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city

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<h3>Job Description</h3>
Job DescriptionSalary: 
Reporting to the Associate Director of Translational Medicine, this individual will serve as an integral team member with exposure to multiple facets of research operations focused on pipeline advancement and evaluation. The Senior Research Associate I / II will be responsible for conducting immunogenicity assays to measure the efficacy of clinical vaccines and work closely with teammates on the organizations Translational Medicine team. Additional functions of the role include performing in vivo mouse experiments to characterize the immune response to the companys lead vaccine candidates.
Elicio (ELTX) is a growing organization based out of the Seaport area of Boston, Massachusetts, with additional staff functioning in a virtual-based environment from the Greater Boston area and throughout the United States.
 Major Duties/Responsibilities
<ul>
<li>Execute immunogenicity and/or biomarker assays to evaluate correlates of response to therapeutic vaccination, such as ELISPOT/Fluorospot, ICS, and other flow cytometry-based assays</li>
<li>Complete experimental documentation and data analysis following appropriate SOPs for investigations on clinical samples</li>
<li>Perform PBMC isolations from whole blood and leukopak for research and clinical studies</li>
<li>Review and author compliant documents as part of the organizations document life cycle management</li>
<li>Assist with clinical sample management, including sample receipt and maintenance of the clinical sample chain of custody</li>
<li>Perform murine handling, injections, and blood/organ collections</li>
<li>Communicate findings in various forums and interact collaboratively with other team members</li>
<li>Willingness to learn new analytical assays and assist with the advancement of novel T cell and antibody-based assays</li>
<li>Perform job responsibilities in compliance with GCLP guidelines, where applicable</li>
</ul>
Education &amp; Professional Experience
<ul>
<li>BS with 3-5+ years of relevant work experience OR MS with 1-3+ years of experience</li>
<li>Ability to take initiative and produce in a fast-paced environment</li>
<li>Ability to prioritize tasks and consistently demonstrate strong decision-making and judgment skills</li>
<li>Strong attention to detail, organizational skills, and the ability to manage multiple projects</li>
<li>Outstanding communication (written and verbal) and interpersonal skills</li>
<li>This position is based in our Boston office and requires on-site presence</li>
</ul>
Working Conditions
<ul>
<li>Busy office/laboratory environment with frequent deadlines and interruptions</li>
</ul>
 
Travel
<ul>
<li>Travel is not required</li>
</ul>
 
Physical Requirements
<ul>
<li>Subject to periods of sitting or standing, vision is required to monitor data. Work is performed exclusively in an office/laboratory environment.</li>
</ul>
 
About Elicio Therapeutics
Elicio Therapeutics, Inc. (Nasdaq: ELTX) is a clinical-stage biotechnology company advancing novel immunotherapies for the treatment of high-prevalence cancers, including mKRAS-positive pancreatic and colorectal cancers. Elicio intends to build on recent clinical successes in the personalized cancer vaccine space to develop effective, off-the-shelf vaccines. Elicios Amphiphile (AMP) technology aims to enhance the education, activation and amplification of cancer-specific T cells relative to conventional vaccination strategies, with the goal of promoting durable cancer immunosurveillance in patients. Elicios ELI-002 lead program is an off-the-shelf vaccine candidate targeting the most common KRAS mutations, which drive approximately 25% of all solid tumors. Off-the-shelf vaccine approaches have the potential benefits of low cost, rapid commercial scale manufacturing, and rapid availability of drug to patients especially in neo-adjuvant settings and for prophylaxis in high-risk patients, contrary to personalized vaccines approaches. ELI-002 is being studied in an ongoing, randomized clinical trial in patients with mKRAS-positive pancreatic cancer who completed standard therapy but remain at high risk of relapse. ELI-002 also has been studied in patients with mKRAS-positive colorectal cancer (CRC) in Phase 1 studies. The updated AMPLIFY-201 Phase 1 data for PDAC and CRC was presented at the ESMO Immuno-Oncology Congress 2024 and included a 16.3-month median recurrence-free survival and 28.9-month median overall survival for the full study population. In the future, Elicio plans to expand ELI-002 to other indications including mKRAS positive lung cancer and other mKRAS positive cancers. Elicios pipeline includes additional off-the-shelf therapeutic cancer vaccines candidates, including ELI-007 and ELI-008, that target BRAF-driven cancers and p53 hotspot mutations, respectively. For more information, please visit <a href="http://www.elicio.com" target="_blank">www.elicio.com</a>.
 
About the Amphiphile Platform 
Elicios proprietary AMP platform delivers investigational immunotherapeutics directly to the brain center of the immune system the lymph nodes. Elicio believes this site-specific delivery of disease-specific antigens, adjuvants and other immunomodulators may efficiently educate, activate and amplify critical immune cells, potentially resulting in induction and persistence of potent adaptive immunity required to treat many diseases. In preclinical models, Elicio observed lymph node-specific engagement driving therapeutic immune responses of increased magnitude, function and durability. Elicio believes its AMP lymph node-targeted approach will produce superior clinical benefits compared to immunotherapies that do not engage the lymph nodes based on preclinical studies.
 
Elicios AMP platform, originally developed at the Massachusetts Institute of Technology, has broad potential in the cancer space to advance a number of development initiatives through internal activities, in-licensing arrangements or development collaborations and partnerships.
 
The AMP platform has been shown to deliver immunotherapeutics directly to the lymph nodes by latching on to the protein albumin, found in the local injection site, as it travels to lymphatic tissue.

Senior Research Associate

<h3>Job Description</h3>
Job DescriptionDescription:
At Terra Fertility, we are reimagining fertility care by making it more accessible through transparent pricing, innovative technology, and comprehensive patient education. We aim to ensure that everyone—regardless of background, language, or identity—feels informed, empowered, and supported throughout their fertility journey.
 
Role Summary
We are seeking a highly skilled and experienced Senior Embryologist to join our IVF laboratory team in Dedham, Massachusetts. The ideal candidate will bring at least 5 years of hands-on experience in embryology, including advanced techniques such as ICSI, PGTA, cryopreservation, and embryo biopsy. The Senior Embryologist will collaborate with clinical, laboratory, and administrative teams to support excellent patient outcomes and operational excellence.
 
Key Responsibilities
<ul>
<li>Perform ICSI, embryo biopsy (e.g., trophectoderm biopsy), and vitrification with high accuracy and success rates.</li>
<li>Support daily operations of the embryology lab including quality control, media preparation, equipment maintenance, and documentation.</li>
<li>Assist with oocyte retrievals, including assessment and preparation of oocytes and semen samples.</li>
<li>Perform fertilization assessments, embryo culture, grading, and cryopreservation.</li>
<li>Adhere to strict quality assurance, double-verification, and safety protocols to maintain lab integrity.</li>
<li>Support embryo transfer processes and communicate with physicians and nursing teams as needed.</li>
<li>Maintain accurate and timely records in laboratory information systems.</li>
<li>Ensure compliance with all regulatory requirements (e.g., CLIA, FDA, OSHA).</li>
<li>Participate in data review, protocol optimization, and lab performance improvement initiatives.</li>
<li>Provide mentorship and training to junior embryology staff.</li>
<li>Support research and validation projects as needed.</li>
</ul>
Work Schedule and Compensation
 
<ul>
<li>This is a full-time, salaried, exempt position. This role is 40 hours/week. </li>
<li>The compensation for this role is $120-170,000, commensurate with experience and qualifications.</li>
<li>Eligible for a generous bonus based on individual and clinic performance. </li>
<li>Comprehensive health, dental, and vision insurance. </li>
<li>401(k) with employer match beginning on day one. </li>
<li>Paid Time off </li>
<li>Support for professional development and ongoing education. </li>
<li>Inclusive, mission-driven workplace environment. </li>
</ul>
Accessibility and Inclusion 
Terra Fertility is committed to fostering an inclusive, diverse, and equitable work environment. We are proud to be an equal opportunity employer. Reasonable accommodations are available upon request during the hiring process or on the job for individuals with disabilities. 
As a condition of employment, Terra Fertility requires all team members to be fully vaccinated against COVID-19 and influenza. Reasonable accommodations will be considered in accordance with applicable laws. 
 
Accommodations
Terra Fertility is committed to providing equal employment opportunities to all individuals. If you require a reasonable accommodation during the application or interview process, or to perform the essential functions of this role, please contact our team at <a href="mailto:info@terrafertility.com" target="_blank">info@terrafertility.com</a>. We will work with you to meet your needs in accordance with applicable law.
 
 
Requirements:
<ul>
<li>Bachelor’s degree in Biology, Biomedical Sciences, or related field required.</li>
<li>Minimum of 5 years of hands-on embryology lab experience, preferably in a high-volume IVF setting.</li>
<li>Proficiency in ICSI, embryo vitrification/warming, egg vitrification embryo biopsy, and embryo culture techniques.</li>
<li>PGT-A biopsy experience strongly preferred.</li>
<li>Strong working knowledge of embryology laboratory equipment, regulatory standards, and best practices.</li>
<li>Detail-oriented with exceptional accuracy and problem-solving skills.</li>
<li>Excellent communication and collaboration with multidisciplinary teams.</li>
<li>Flexible and reliable, with availability for early mornings and occasional weekend or holiday shifts if needed.</li>
</ul>

Senior Embryologist

<h3>Job Description</h3>
Job Description
Title: Undergraduate HTE Research Co-op (Spring - Summer 2026)
Adimab is the leading technology provider for therapeutic antibody drug discovery, focusing solely on our partnerships without pursuing an internal product pipeline. Since 2009, we have partnered with over 130 pharmaceutical and biotechnology companies, generating more than 600 therapeutic programs, of which more than 75 have entered clinical trials.&nbsp;&nbsp;
Role
We are seeking a motivated student&nbsp;to join our High Throughput Expression Group for approximately 40 hours per week, with the potential for minimum (2-4 hours) weekend work. The successful candidate will provide support on the following tasks:
Responsibilities
<ul>
<li>Media formulation</li>
<li>Yeast culture maintenance</li>
<li>Routine platform affinity purification</li>
</ul>
Needed upon hire
<ul>
<li>Working towards degree in Biotechnology, Bioengineering, or a related field</li>
<li>Detail oriented</li>
<li>Ability to commit to a 6-month term starting in January 2026</li>
<li>Knowledge of basic wet bench skills and laboratory safety</li>
<li>Adaptable and productive in a fast-paced environment</li>
<li>Ability to communicate effectively and openly with colleagues and supervisors&nbsp;</li>
<li>Willing to work weekends as needed</li>
</ul>
Come join us!
As a profitable privately-held biotech company, we take a long-term view on value creation and make substantial investments in technology development, research, and our people.&nbsp;
Located in New Hampshire’s beautiful Upper Connecticut River Valley, we are minutes from Dartmouth College, the Geisel School of Medicine, the Thayer School of Engineering, the Tuck School of Business, and the&nbsp;Dartmouth Hitchcock&nbsp;Medical Center. We are fortunate to be situated in an area that is renowned for its premier skiing, hiking, and biking.
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Undergraduate HTE Research Co-op (Spring - Summer 2026)

<h3>Job Description</h3>
Job DescriptionTumor Ex-vivo Research Associate (6 month contract role) Position Summary We are seeking a highly motivated Research Associate on a 6 month contract basis to join the Primary Cell Platform (PCP) Team within the Immunology and Pharmacology Department at PIRC. The candidate will be part of a collaborative and fast-paced team driving preclinical research focused on human tumor biology and immune function. The role offers the opportunity to work with clinically relevant human samples and contribute to translational research efforts that support early-stage therapeutic discovery. A strong candidate will have a background in immunology and/or cell biology, with prior hands-on experience in cellular assays, tissue culture, or immunoassays. The ability to work effectively within multidisciplinary teams, follow complex protocols, and deliver high-quality experimental data is essential. This is an excellent opportunity to gain experience in advanced tumor modeling and immunoprofiling techniques while supporting impactful, real-world research. This is a 6 month contract with potential to transition to a full-time permanent role based on performance and project success. Upon conversion, the employee will be eligible for our full benefits package. &nbsp;Main Responsibilities
<ul>
<li>Perform in vitro and ex vivo experiments focused on tumor-immune interactions using primary human models</li>
<li>Support the culture and maintenance of primary tumor tissues, including tumor slice assays, spheroids/organoids, and immune co-cultures</li>
<li>Process tumor/blood specimens: e.g. tissue dissociation, PBMC isolations from whole blood, viability assessment, and assay preparation</li>
<li>Execute immunological assays such as:
<ul>
<li>Flow cytometry, ELISA, MSD, cytokine profiling</li>
<li>T cell activation, proliferation, and cytotoxicity assays</li>
</ul>
</li>
<li>Culture primary human immune cells (e.g., PBMCs, T cells, macrophages)</li>
<li>Analyze and interpret experimental data and present findings to the team</li>
<li>Maintain detailed, timely, and compliant documentation using an electronic lab notebook (ELN)</li>
<li>Follow lab safety and quality standards</li>
<li>Be available for occasional after-hours work to support time-sensitive tumor sample processing</li>
</ul>
Basic Qualifications
<ul>
<li>Bachelors/Masters degree in Immunology, Cell Biology, Biomedical Sciences, or a related life science field with 2-3 years of industrial experience</li>
<li>Available to work full-time, onsite for the 6 months duration without needed work authorization/sponsorship from the company</li>
</ul>
Preferred Qualifications
<ul>
<li>Previous relevant laboratory experience is highly preferred</li>
<li>Skilled in aseptic technique and primary human cell culture</li>
<li>Experience with tumor tissue handling, 3D culture systems, or ex vivo tumor models</li>
<li>Familiarity with flow cytometry, immunoassays, and related technologies</li>
<li>Experience using an electronic lab notebook for experimental documentation</li>
<li>Excellent communication, time management, and organizational abilities</li>
<li>Collaborative, flexible, and motivated to work in a fast-paced translational research environment</li>
</ul>
 &nbsp;
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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Tumor Ex-vivo Research Associate (6 month contract role)

<h3>Job Description</h3>
Job DescriptionSenior/Principal Scientist, Translational Sciences Job summary: PharmaEssentia Innovation Research Center (PIRC) is seeking a highly motivated and experienced senior or principal scientist to join our Translational Sciences team and contribute to the development of first-in-class and best-in-class biotherapeutics, including cytokines, antibodies, and antibody-drug-conjugates. The successful candidate will contribute to the design, execution, and interpretation of translational biomarker and mechanism of action (MOA) studies to support the development and regulatory approval of novel therapeutics as they transition from late discovery into first in human clinical trials and beyond. In this position, you will utilize your expertise in pharmacokinetics, pharmacodynamics, and biomarker discovery to guide drug development and biomarker strategies, optimize dosing regimens, and ensure the safety and efficacy of investigational drugs. You will also contribute to translational activities aimed at maximizing the potential of BESREMI, PharmaEssentia’s marketed drug for the treatment of myeloproliferative neoplasms. These efforts include indication expansion, novel combinations, and refining/improving biomarker approaches to guide dosing and patient selection. Additionally, you will provide scientific leadership, mentorship, and cross-functional collaboration within the Translational Sciences team and across other departments. The Company: It’s not often that you get the chance to make a real impact on the lives of others, while expanding your own possibilities. You’ll find that rare opportunity at PharmaEssentia. Join us, and let’s transform lives, together. PharmaEssentia Corporation is a rapidly growing biopharmaceutical innovator. We are leveraging deep expertise and proven scientific principles to deliver effective new biologics for challenging diseases in the areas of hematology, oncology and immunology, with one approved product and a diversifying pipeline. We believe in the potential to improve both the health and quality of life for patients with limited options today through the combination of rigorous research and innovative thinking. Founded in 2003 by a team of Taiwanese American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taipei Exchange (TPEx: 6446) and are expanding our global presence with operations in the U.S., Japan, China and Korea, along with a world-class biologics production facility in Taichung. Our new research center, PharmaEssentia Innovation Research Center (PIRC), will build upon our invention and discovery-based innovation efforts originally established in Taiwan that led to a transformative advancement for treating polycythemia vera (one of the myeloid proliferative neoplasms). At PIRC, we aim to expand our current expertise in related therapeutic areas and identify novel therapeutic approaches in early to mid-stage discovery and development. Data scientists will leverage artificial intelligence and machine learning to inform new target and indication selection. The company is also recruiting for talented scientists who have deep knowledge in immunology, translational science, bioinformatics and biologics platforms to develop novel drugs leveraging disease-driving biology, novel technology in protein engineering, antibody discovery and new modalities. Summary of Key Responsibilities:
<ul>
<li>Study Design and Execution: Lead the design, planning, and execution of translational studies in indication-relevant animal models and primary human cellular and tissue systems to identify and validate biomarkers and explore drug candidate mechanism of action. Collaborate with cross-functional teams to ensure alignment with discovery and development goals as well as regulatory requirements.</li>
<li>Further Exploration of BESREMi: Collaborate with clinical development team to further explore the potential of BESREMi in MPN and other areas of Oncology. Conduct translational studies internally and be involved in investigator-initiated trials (IITs) or company sponsored clinical trials to maximize the clinical potential of BESREMi.</li>
<li>Data Analysis and Interpretation: Oversee the analysis, interpretation, and reporting of in vitro and in vivo pharmacology/translational biomarker data, including pharmacokinetic and pharmacodynamic parameters, exposure-response relationships, and safety/tolerability profiles. Provide scientific insights to inform decision-making and optimize study outcomes.</li>
<li>Drug Development Strategy: Contribute to the development and implementation of clinical pharmacology strategies to support the progression of investigational drugs through all phases of clinical development. Generate scientific rationale for dose selection, formulation optimization, and therapeutic target validation.</li>
<li>Regulatory Interaction: Work with regulatory affairs to support the preparation and review of regulatory submissions, including investigational new drug (IND) applications, new drug applications (NDAs), and marketing authorization applications (MAAs). Address inquiries and provide scientific justifications for study designs, endpoints, and data analyses.</li>
<li>Scientific Leadership: Serve as a subject matter expert in translational biomarkers, target biology and candidate therapeutic mechanism of action, providing guidance and mentorship to junior scientists, clinicians, and project teams. Contribute to the scientific literature through publications, presentations, and participation in professional conferences and working groups.</li>
<li>Cross-Functional Collaboration: Collaborate closely with colleagues in data sciences, biologics, immunology/pharmacology, clinical development, and regulatory affairs to integrate translational biomarker and mechanism of action insights into overall drug development strategies. Foster a culture of scientific excellence, innovation, and collaboration.</li>
</ul>
Qualifications:
<ul>
<li>Ph.D. in oncology, immunology, immuno-oncology, pharmacology, pharmaceutical sciences, or a related discipline.</li>
<li>3+ (for senior scientist) or 8+ (for principal scientist) years’ experience in the pharmaceutical or biotechnology industries, including a proven track record of leadership and scientific achievement in translational sciences.</li>
<li>Expertise in in vivo model design and biomarker discovery, both internally and via contract research organizations and academic collaborations.</li>
<li>Experience with primary human cellular/tissue-based assays to guide/inform indication selection, biomarker discovery and mechanism of action.</li>
<li>Experience with immuno-oncology and autoimmune disease/chronic inflammation targets and associated in vitro and in vivo models is preferred.</li>
<li>Experience in clinical trial design and/or clinical operations in either company-sponsored, or IIT clinical trials is strongly desirable.</li>
<li>Strong analytical skills, with proficiency in pharmacokinetic/pharmacodynamic software (e.g., NONMEM, Phoenix WinNonlin, R) is preferred.</li>
<li>Experience working closely with academic collaborators via sponsored research agreements or IITs is preferred.</li>
<li>Excellent communication and presentation skills, with the ability to effectively convey complex scientific concepts to diverse audiences.</li>
<li>Demonstrated leadership capabilities, including the ability to mentor and develop talent, foster teamwork, and drive results in a dynamic environment.</li>
</ul>
Conclusion: As a Senior/Principal Scientist in Translational Sciences, you will play a pivotal role in advancing the understanding of drug pharmacology and contributing to the development of innovative therapeutics to address unmet medical needs. Your scientific expertise, leadership skills, and collaborative approach will be critical for driving drug development programs forward and ultimately improving patient outcomes at PIRC.
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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Senior/Principal Scientist, Translational Sciences

<h3>Job Description</h3>
Job DescriptionJob Description The Role: Title: In vivo research associate, Immunology and Pharmacology Job summary: The PharmaEssentia Innovation Research Center is building a world-class new drug discovery team in Boston area. We are seeking a highly motivated in vivo research associate to support in vivo experiment (rodent), including MTD studies, Efficacy studies, PK/PD studies and tissue harvest. You will also be asked to maintain and expand cancer cell lines to support the in vivo tumor model studies and conduct hand-on dosing and procedure support for mice pharmacology studies. In addition, you may need to support all aspects of laboratory operation to maintain a highly productive vivarium/laboratory. The Company: It’s not often that you get the chance to make a real impact on the lives of others, while expanding your own possibilities. You’ll find that rare opportunity at PharmaEssentia. Join us, and let’s transform lives, together. PharmaEssentia Corporation is a rapidly growing biopharmaceutical innovator. We are leveraging deep expertise and proven scientific principles to deliver effective new biologics for challenging diseases in the areas of hematology, oncology and immunology, with one approved product and a diversifying pipeline. We believe in the potential to improve both the health and quality of life for patients with limited options today through the combination of rigorous research and innovative thinking. Founded in 2003 by a team of Taiwanese American executives and renowned scientists from U.S. biotechnology and pharmaceutical companies, today we are listed on the Taipei Exchange (TPEx: 6446) and are expanding our global presence with operations in the U.S., Japan, China and Korea, along with a world-class biologics production facility in Taichung. Our new research center, PharmaEssentia Innovation Research Center (PIRC), aims to leverage our current expertise in oncology and immunology therapeutic areas to identify and develop novel therapeutic opportunities. Therefore, we are recruiting talented scientists who have deep knowledge in immunology, translational science, bioinformatics and biologics platforms to develop novel drugs through disease-driving biology, novel technology in protein engineering, antibody discovery and new modalities. PIRC offers a competitive benefit package, including a competitive 401k match, medical/dental/eye care benefits, and other benefits. Summary of Key Responsibilities:
<ul>
<li>Hand-on execute subcutaneous tumor model studies from cancer cells expansion, implantation (in mice), tumor measurement, group randomization and administration of test articles. </li>
<li>Hand-on support all mice pharmacology study procedures, including but not limiting to dosing and tissue harvest.</li>
<li>Follow PIRC IACUC program/protocols and standard operating procedures (SOPs) for all animal procedures.</li>
<li>Maintain and expand cancer cell lines for human xenograft tumor and mouse syngeneic tumor models. </li>
<li>Data process and graphing for the internal team update presentation.</li>
</ul>
Essential Qualifications:
<ul>
<li>B.S. or higher degree in immunology, pharmaceutical sciences or related scientific field</li>
</ul>
&nbsp;SkillPerformed in the last 2 years (includes training)In vitro assayELISANot required, good to knowMSDNot required, good to knowFACSNot required, good to knowHusbandry&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Aseptic TechniqueMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Micro-Isolator TechniqueMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Restraint &amp; HandlingMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Room ChecksNot required, good to know&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cage ChangeNot required, good to know&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Injections/ Administration&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; SubcutaneousMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; IntraperitonealMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; IntravenousMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; IntramuscularNot required&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Oral GavageNot required, good to knowBlood Withdrawal&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Tail BleedMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cardiac PunctureMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; SubmandibularMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; RO BleedNot required, good to knowEuthanasia&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; CO2 OverdoseMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Cervical DislocationMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; DecapitationNot requiredAnimal Preparation&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; ShavingMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ear TaggingNot required&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Ear Punching/ NotchingNot requiredImplantation&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Xenograft SCMust&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Mammary Fat Pad&nbsp;Good to know&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; TrocarNot required&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Anesthesia&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; Isoflurane AnesthesiaNot required, good to knowLab OperationsGeneral Organizing lab spaceMustReceiving/stocking suppliesMustAny other duties that may ariseMustMammalian Cell CultureStandard mammalian cell culture procedures and associated aseptic techniques in addition to maintenance of tissue culture facilitiesMustMedia and buffer preparation, culture initiation, propagation, and cryopreservation of cells, including primary human and mouse cells and cell lines as well as adherence to quality control schedules for ensuring consistency of cell culture materials.Must &nbsp; EEO Statement: At PharmaEssentia Innovation Research Center (PIRC), we are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants without regard to race, color, religion, sex, pregnancy (including childbirth and related medical conditions), national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information (including characteristics and testing), military and veteran status, and any other characteristic protected by applicable law. PIRC believes that diversity and inclusion among our team are critical to our success as a global company, and we seek to recruit, develop and retain the most talented people from a diverse candidate pool.&nbsp; PIRC does not accept unsolicited agency resumes. Staffing agencies should not send resumes to our HR team or to any PIRC employees. PIRC is not responsible for any fees related to unsolicited resumes from staffing agencies. &nbsp;
At PharmaEssentia, our goal is to treat as many people with cancer as possible. That means challenging the status quo with better science that leads to better lives. By joining our team, you will not only expand your own possibilities, but you will contribute to expanding options for people with cancer.
<a href="https://us.pharmaessentia.com/careers/" target="_blank">https://us.pharmaessentia.com/careers/</a>
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In-vivo Research Associate, Immunology and Pharmacology

<h3>Job Description</h3>
Job DescriptionJob Title: Process Chemistry Contractor Location: Cambridge, MA, 02139 Duration:12+ months (Possibilities of Extension) Work Shift: : 5 days onsite in the lab. Pay Rate: $43/Hour on W2 Job Description Summary: Duties: Seeking an exceptional organic chemist to join our Process Chemistry group. This contract position resides within the Pharmaceutical Sciences organization. The candidate will work full-time onsite and execute laboratory activities related to the development of robust drug substance manufacturing processes across various phases of drug substance development. The ideal candidate will conduct multi-step organic synthesis, route scouting and optimization, purification and characterization of intermediates and final compounds to support drug substance scale-up activities. An ideal candidate will have a strong foundation in modern synthetic organic chemistry and analytical techniques such as NMR, LCMS, UPLC/HPLC (Empower proficiency) and an understanding of early drug development processes and experiments. Experience in small-molecule process development and scale up is highly desired, however not required. Responsibilities: • Participate in the design, planning and execution of multi-step synthesis, process research and development as a cross-functional team member. • Collaborate with cross-functional teams to ensure successful project outcomes. • Implement process enhancements, scientific approaches and technical improvements to deliver robust chemical processes. • Document and report experimental results and findings. • Draft and review technical documents (development reports, patent applications, tech transfer documents etc.) • Maintain an accurate, timely and compliant laboratory notebook. • Maintain laboratory equipment and ensure compliance with safety regulations. Skills: Qualifications: • Strong knowledge of organic chemistry. • Experience with early phase route development and process optimization • Proficiency in using analytical instruments (HPLC/UPLC, NMR, LCMS) and software. • Strong analytical and problem-solving skills. • Strong written and verbal communication skills. • Ability to work independently and as part of a team. • Strong organizational and time management skills. Capabilities: • Ability to effectively prioritize and manage multiple tasks and compounds • Ability to adapt to change and to work optimally within a variety of situations • Ability to build productive working relationships across functions and highly diverse groups of individuals • Self-motivated and willing to “learn on the job” and ask for assistance when needed • Ability to make a significant impact in a results-driven environment where accountability is key. • A team player, who listens effectively and invites response and discussion • A collaborator who communicates in an open, transparent, complete, timely and consistent manner Education: 
<ul>
<li>An ideal candidate would have a B.S. or M.S. in Chemistry, or a related field with 3+ years of experience in pharmaceutical research or laboratory setting or, Ph.D. with 0-3 years of experience.</li>
</ul>
 #sczr2

Process Chemistry Contractor

<h3>Job Description</h3>
Job DescriptionAbout Us
Merryfield Investment Management, Inc. is a leading investment management firm that specializes in providing personalized investment solutions to high-net-worth individuals, institutions, and foundations. With a client-centered approach and a team of experienced professionals, we aim to help our clients achieve their financial goals through disciplined and calculated investment strategies.
About the Job
Merryfield Investment Management, Inc. is seeking a highly skilled Quantitative Analyst to join our dynamic team. As a Quantitative Analyst, you will be responsible for conducting in-depth research and analysis of market trends and data to help inform our investment decisions. You will utilize your strong quantitative and analytical skills to provide insights that drive performance and enhance our clients' portfolios.
Responsibilities
<ul>
<li>Develop, maintain and enhance quantitative models and tools for analyzing investment opportunities and tracking portfolio performance.</li>
<li>Conduct extensive research and analysis of market trends, economic indicators, and company financial data.</li>
<li>Collaborate with portfolio managers to identify investment opportunities and make data-driven investment decisions.</li>
<li>Perform statistical and data analysis to identify investment trends and opportunities within various market sectors.</li>
<li>Monitor and evaluate risk metrics, including value-at-risk, stress testing, and exposure analysis, to ensure effective portfolio management.</li>
<li>Utilize programming skills to develop and automate data collection, analysis, and reporting processes.</li>
<li>Present findings and insights to the investment team and assist in the formulation and implementation of investment strategies.</li>
<li>Stay up-to-date with industry developments and best practices to continuously improve our quantitative processes.</li>
</ul>
Requirements
<ul>
<li>Bachelor's or Master's degree in Mathematics, Statistics, Quantitative Finance, or a related field.</li>
<li>3-5 years of experience as a Quantitative Analyst, preferably in the investment management industry.</li>
<li>Strong analytical and problem-solving skills with a keen attention to detail.</li>
<li>Proficient in statistics, econometrics, and programming languages such as SAS, R, Python, or MATLAB.</li>
<li>Excellent communication and presentation skills, with the ability to clearly communicate complex quantitative concepts to non-technical stakeholders.</li>
<li>Knowledge of financial markets and investment products, with a deep understanding of risk management principles.</li>
<li>Ability to work independently and collaboratively in a fast-paced, deadline-driven environment.</li>
<li>CFA or FRM certification is a plus.</li>
</ul>
Bonus Points
<ul>
<li>Paid parental leave</li>
<li>Parental leave</li>
<li>Health insurance</li>
<li>401(k) matching</li>
<li>Paid time off</li>
<li>Vision insurance</li>
<li>Dental insurance</li>
</ul>

Quantitative Analyst

<h3>Job Description</h3>
Job Description
Discover Veranova
At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focuses on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference.
Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. 
Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. 
Role Overview:
We’re seeking a motivated scientist to support the development of next-generation antibody-drug conjugates (ADCs). In this role, you’ll perform hands-on conjugation and purification experiments with antibodies, peptides, and oligonucleotides, optimizing processes that directly impact the success of innovative therapeutics. Working under the guidance of experienced technical leads, you’ll gain valuable experience while contributing to projects that drive real-world impact.
Core Responsibilities: 
<ul>
<li>Develop and implement phase appropriate bioconjugation development strategies for the attachment of cytotoxic payloads, peptides, oligonucleotides, or other small molecules to antibodies, proteins, peptides, or other therapeutic entities.</li>
<li>Delivers experimental output with a high degree of scientific integrity, schedule and target adherence, and quality with guidance. </li>
<li>Exhibits safety awareness by conducting lab and other operations in a safe manner and holding themselves accountable for safe behavior in the work environment. </li>
<li>Act on feedback and shows continuous commitment to learning and development.</li>
<li>Makes efforts towards independently working and consistently meeting deadlines.</li>
<li>Keeps accurate, legible and complete records of all experiments, observations, and equipment. </li>
<li>Writes high quality reports and delivers presentations to customers and management with some guidance in alignment with the project milestones.</li>
<li>Builds an understanding of process chemistry for developing active pharmaceutical ingredients.</li>
<li>May maintain technical equipment.</li>
<li>Accomplishes other duties which are within the employee’s skills and abilities per reasonable request.</li>
</ul>
Qualifications: 
Required
<ul>
<li>Bachelor’s degree (or equivalent experience) in a chemistry related discipline.</li>
<li> </li>
<li>Experience with bioconjugation lab and analytical techniques desired.</li>
<li>Ability to write clear and concise technical reports.</li>
<li>Good understanding of Microsoft Office and other relevant technical software platforms</li>
<li>Good written and verbal communication skills.</li>
<li>Ability to work independently and in a team environment.</li>
</ul>
Preferred
<ul>
<li>Master’s degree (or equivalent experience) in a chemistry related discipline.</li>
</ul>
Special Factors 
<ul>
<li>While performing the duties of this job it is required to stand, walk, and use hands to operate objects, tools, or controls; reach with hands or arms; climb, balance, stoop, kneel, or crouch when necessary for the job activity.</li>
<li>Must be able to lift and/or move up to 50 pounds.</li>
<li>Specific vision abilities include: near, distance, peripheral, color perception, and the ability to adjust focus.</li>
<li>Regularly works with moving mechanical parts and may work with toxic or caustic chemicals. </li>
<li>The work may be performed in humid areas with low or high temperatures. </li>
<li>This work may need to work with a respirator or operate with full-body Tyvek suits and supplied air or PAPR.</li>
</ul>
Our Commitment:
<ul>
<li>Health &amp; Wellness: Comprehensive health &amp; Wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. </li>
<li>Financial Wellness: Comprehensive total compensation package that includes competitive base salary, Defined Contribution Pension program, eligibility for performance-based bonuses, and attractive 401(k) Plan with company match.</li>
<li>Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs.</li>
<li>Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We are committed to ensuring that everyone can bring their full self to work and thrive in their career.</li>
</ul>
How to Apply: 
At Veranova, we are on a misson to meet people that believe in our values and can contribute to the team in a variety of ways. Please visit <a href="http://www.veranova.com" target="_blank">www.veranova.com</a> to view all open roles and join our Talent Community to stay connected and learn about opportunities as they arise. 
We value a range of experiences and perspectives. If you want to be part of improving and saving the lives of patients, we encourage you to apply regardless of whether you meet every qualification listed. 
For applicants who may require a reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email to <a href="mailto:talentacquisition@veranova.com" target="_blank">talentacquisition@veranova.com</a> in order to confirm your request for an accommodation. Please include the job number, title, and location of role. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Veranova employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Additional Information:
Applicants for this role must be authorized to work in the United States without further employer sponsorship. 
Agency and Search Firm Representatives: Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. 
Important Notice Regarding Recruitment Scams: Veranova is committed to providing professional and secure recruitment experience for all applicants. Unfortunately, fraudulent job postings and recruitment scams are becoming more prevalent. We want to ensure that all candidates are aware of potential scams. Please see our notice here.
<ul>
<li>Legitimate communications from Veranova will only come from official email addresses using our domain: veranova.com.</li>
<li>Legitimate LinkedIn communications will only come from active Veranova employees.</li>
<li>Veranova will never ask candidates for sensitive personal information during the application process (e.g., bank account details or social security number).</li>
<li>Veranova will never ask candidates for payment (e.g., for equipment, training, or background checks).</li>
</ul>
All your information will be kept confidential according to EEO guidelines.
Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law.
All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice.
#LI-Onsite

Associate Scientist - Bioconjugation

<h3>Job Description</h3>
FM is a leading property insurer of the world's largest businesses, providing more than one-third of FORTUNE 1000-size companies with engineering-based risk management and property insurance solutions. FM helps clients maintain continuity in their business operations by drawing upon state-of-the-art loss-prevention engineering and research; risk management skills and support services; tailored risk transfer capabilities; and superior financial strength. To do so, we rely on a dynamic, culturally diverse group of employees, working in more than 100 countries, in a variety of challenging roles.
 
Provide technical support in the performance of Research and Approvals tests conducted at the FM Research Campus, primarily in the Large and Small Burn Laboratories, under the direction of the General Foreman. Day-to-day activities includes test setup, instrumentation and equipment troubleshooting as well as firefighting and cleanup efforts.
 
High School/Trade School or Military specialist training with 3 years general mechanical or electrical experience.
1 year laboratory experience preferred.
Experience with or knowledge of product assembly, equipment repair, use of hand and power tools, welding/fabrication, use of instrumentation and sensors and computer literacy.&nbsp;
Must be able to commute to the FM Research Campus in West Glocester, RI.
Must be able to fulfill the physical requirements of the job (applies to all Labs, LBL, SBL, Remote Test Site, Earthquake Lab,&nbsp;and Campus Work Areas) including:
<ul>
<li>Ability to lift 50 pounds</li>
<li>Ability to climb stairs and ladders</li>
<li>Ability to work at heights</li>
<li>Ability to operate vehicles, lift trucks, fork trucks,&nbsp;other vehicles</li>
<li>Must be able to work while wearing full Firefighter’s Turnout gear with SCBA for an extended period of time in a wet and smoky environment</li>
<li>Must be able to obtain certification&nbsp;for using a personal respirator and work while wearing one for an extended period of time in a wet and smoky environment</li>
<li>Must not be claustrophobic and be able to work in tight and cramped spaces</li>
<li>Must have a current US Driver’s License</li>
<li>Must be able to communicate effectively in English</li>
<li>Must be able to work while wearing a Fall Protection Harness</li>
<li>Candidate must have the ability to read, write and speak English proficiently and the ability to understand and follow English instructions.</li>
</ul>
The final salary offer will vary based on geographic location, individual education, skills, and experience. The position is eligible to participate in FM's comprehensive Total Rewards program that includes an incentive plan, generous health and well-being programs, a 401(k) and pension plan, career development opportunities, tuition reimbursement, flexible work, time off allowances and much more.&nbsp;
FM is an Equal Opportunity Employer and is committed to attracting, developing, and retaining a diverse workforce.
#LI-TA1

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