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<h3>Job Description</h3>
Job DescriptionCompany Description 
<ul>
<li>Katalyst Healthcares &amp; Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.</li>
<li>We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.</li>
</ul>
Job Description 
Job Description:
The Associate QC Scientist performs laboratory testing within a fast paced GMP environment in support of one or more of the following areas; raw materials, in-process product, final Bulk product, stability, and/or validation. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but is able to manage time efficiently in achieving timely completion of assigned duties. Assists in trending data to support assay performance. Assists in writing lab Investigation reports.
Responsibilities
<ul>
<li>Performs test methods as written to support product/material release.</li>
<li>Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.</li>
<li>Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.</li>
<li>Will perform a multitude of laboratory techniques for which they are trained.</li>
<li>Accepts responsibility to complete assigned tasks as committed. works with others to maintain a positive atmosphere to accomplish business objectives.</li>
<li>Revises procedures as necessary and provides support for department.</li>
<li>Helps maintain trend reports, which support departmental performance.</li>
<li>Support investigations.</li>
<li>Will effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.</li>
</ul>
Requirements
<ul>
<li>BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.</li>
<li>3 + years of related work experience.</li>
</ul>
Additional Information 
All your information will be kept confidential according to EEO guidelines.

Chemist II

<h3>Job Description</h3>
Job Description
Job Description 
<ul>
<li>
As a Senior Scientist, you will be at the center of our operations and you'll find that everything we do, every day, is in line with an unwavering commitment to quality. 
</li>
<li>
As part of the upstream mammalian team within Manufacturing Sciences and Technology (MSAT) you will be responsible for process troubleshooting, process improvements and second-generation process development of late-stage commercial biopharmaceuticals and vaccines.
</li>
<li>
Through laboratory scale process development and transfer to commercial stages, you will partner with manufacturing specialists for drug substance production and provide support for technology transfer to manufacturing sites and third-party facilities. 
</li>
<li>
Your innovative mindset will help us develop economical, efficient and safe active APIs.
</li>
<li>
Be recognized as a technical expert and scientific contributor. 
</li>
<li>
With your deep knowledge of mammalian cell culture and bioreactor engineering you will be an active team member whose decisions impact the project. 
</li>
<li>
Use your scientific judgement to adapt standard methods and techniques by applying prior work experience. 
</li>
<li>
Be forecasting and planning resource requirements for your project team. 
</li>
<li>
Your creativity in developing novel processes and new ideas will be used frequently. 
</li>
<li>
Undertake mentoring activities to guide team members.
</li>
<li>
It is your innovative scientific temperament that will help in making ready to achieve milestones and new patients across the globe.
</li>
</ul>
Qualifications:
<ul>
<li>
Minimum Bachelor's degree in relevant scientific discipline
</li>
<li>
BA and PhD candidates welcome
</li>
<li>
Biochemical engineering
</li>
<li>
Mammalian Cell Culture
</li>
<li>
Bioreactor operation
</li>
<li>
Antibody production
</li>
<li>
Experience must be beyond education/hands on in the field
</li>
<li>
6+ years of experience in bioprocessing
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

MSAT Snr Scientist

<h3>Role Summary </h3>
<ul>
<li> Responsibilities: You will take a leading role across a variety of medical communication projects, working alongside a team of excellent colleagues to ensure that projects are delivered to an exceptionally high standard</li>
<li> Salary: $90,000 to $94,000 per annum, depending on your qualifications and previous experience (please note that we have established salary bands that are determined by your level of educational attainment and relevant experience to ensure a fair and consistent approach for all applicants, eliminating the need for individual negotiations)</li>
<li> Benefits: Discretionary profit share bonuses paid twice per year, hybrid and flexible working options, generous vacation allowance, private medical and dental insurance, 401K plan with up to a 5% employer contribution, life insurance, full funding and study leave for external training and <a href="https://www.costellomedical.com/careers/working-at-costello-medical/benefits-package-in-the-us/" target="_blank">more</a> </li>
<li> Role Type: Full-time, permanent</li>
<li> Start Date: We are currently recruiting for start dates throughout 2025, and we can offer both immediate and deferred start dates. You will be asked to state your availability on your application form</li>
<li> Application Deadlines: Whilst there are no set application deadlines, we strongly recommend applying as early as possible. The role will close when suitable candidates are found</li>
<li> Location: This role is based in our <a href="https://www.costellomedical.com/careers/locations/working-in-boston/" target="_blank">Boston, MA</a> office</li>
</ul>
<h3>About the Role</h3>
Costello Medical are growing quickly through demand from both new and existing clients and are therefore looking for candidates with prior experience in medical affairs and/or publications who enjoy content delivery, as well as project and client management, to join us as Senior Medical Writers in our <a href="https://www.costellomedical.com/what-we-do/medical-communications/" target="_blank">Medical Communications</a> team. In this role, you will be at the forefront of our exciting expansion in the US market. This is a unique opportunity to influence and drive change in our fast-growing company, in a role you can shape to be your own, where we can offer excellent career development opportunities to high performing individuals. 
Senior Medical Writers take a leading role across projects, providing strategic advice to clients, supervising the project team, and producing high-quality scientific content themselves. They ensure projects are delivered to an exceptionally high standard and in line with agreed timelines. This role involves regular client communication, project planning, reviewing colleagues’ work, providing constructive feedback, scientific writing and contributing to business development by identifying new clients, writing proposals, and building and maintaining excellent client relationships.
You will be based in our office in <a href="https://www.costellomedical.com/careers/locations/working-in-boston/" target="_blank">Boston</a>, which was established in 2020. This presents opportunities to shape and drive our US company, whilst being supported by the success of our existing operations in the UK and Asia. You will work closely with our Boston-based Team Heads, who each have 7–10+ years of experience in the industry, as well as other senior colleagues in the US and globally.
Hybrid Working Policy: We believe that having face-to-face time in the office holds many benefits and is central to ensuring that the community we have created, where people have a workplace they belong to and feel part of, is never lost. At the same time, we recognise that homeworking can improve work life balance, reduce commuting times and costs, and provide the opportunity to juggle personal commitments. Therefore, we offer flexible working arrangements that allow our colleagues to work from home for up to half of the time, measured across a 2-week rolling period. 
<h3>Why Join Costello Medical as a Senior Medical Writer?</h3>
At Costello Medical we think that the road to success is through investing in and developing our talent. Because of that philosophy, we believe that our environment is the perfect place to grow your career, and here are a few reasons why: 
<ul>
<li> We are invested in our culture: We make it a priority to create an energetic, fun and supportive work environment while still delivering the highest standard of work to our clients. As a result, we achieved our B Corp certification in 2022</li>
<li> Join us early in our US venture: Our US operations are relatively new and growing quickly, presenting unique opportunities for professional growth. We are onboarding multiple new hires across various roles every month, offering a dynamic and evolving work environment. This is the perfect time to join and contribute to shaping the future of our operations</li>
<li> Our range of expertise: Whilst you will be primarily working on Medical Communications projects, you may also have the opportunity to work on projects for our different service offerings, including Value and Access, Rare Diseases and Evidence Development, collaborating with colleagues in a range of positions and specialisms</li>
<li> The varied responsibilities: You will have the unique opportunity to continue to develop your scientific writing expertise, whilst using your communication skills to build strong and long-lasting client relationships</li>
<li> Have a real-world impact: Our clients are some of the preeminent pharmaceutical and medical technology companies in the industry. We are committed as an organization to improve health outcomes globally, and you will get the chance to take a leading role in this vision</li>
</ul>
<h3> Career Profile</h3>
We offer many opportunities for personal and professional development at Costello Medical. Please click below to read firsthand accounts from our colleagues about their time with the company: <a href="https://www.costellomedical.com/careers/working-at-costello-medical/" target="_blank">https://www.costellomedical.com/careers/working-at-costello-medical/</a> 
<h3>About Costello Medical </h3>
Costello Medical is a rapidly growing global healthcare agency specializing in medical communications, market access and health economic and outcomes research. We work with a wide range of clients, including the industry’s most successful pharmaceutical companies. We received B Corporation Accreditation in 2022. Please click here to learn more about us, our work and our mission: <a href="https://www.costellomedical.com/" target="_blank">https://www.costellomedical.com/</a>&nbsp; 
Requirements
<h3> About You</h3>
Essential requirements for the role are:
<ul>
<li>A degree level or higher qualification in a scientific discipline (minimum GPA 3.3). We welcome applications from candidates with a diverse range of specialisms, including but not limited to; biology, chemistry, pharmacy and medicine</li>
<li>At least 2 years’ professional experience in a medical communications (medical affairs and/or publications) role outside of academia, ideally within an agency setting</li>
<li>Strong scientific writing skills with the ability to tailor writing style to different audiences</li>
<li>Project management skills sufficient to enable timely project delivery</li>
<li>Exceptional attention to detail and high degree of written accuracy</li>
<li>Excellent proficiency in written English and arithmetic</li>
<li>Experience with supporting junior colleagues with their learning and development </li>
<li>Excellent data presentation skills, including the ability to use Excel, PowerPoint and Word effectively and efficiently, to produce a professional, high standard of work</li>
<li>Sufficient technical and strategic knowledge to provide clients with recommendations on project content and approach</li>
<li>The capacity to maintain exceptional customer service and quality of deliverables under multiple competing demands </li>
<li>Experience in communicating directly with clients, including responding to different communication styles, as well as a proven ability to build robust and sustainable client relationships</li>
<li>The ability to motivate colleagues and take a leadership role in the delivery of project components</li>
</ul>
Whilst we are seeking applications from those who already have at least 2 years experience delivering projects in medical communications, we are seeking those who are flexible and willing to contribute to a wide variety of projects. You will be expected to work across different accounts spanning multiple disease areas and therefore should be able to familiarize yourself with new information quickly.
Benefits
<h3>What We Offer </h3>
Alongside our award-winning company culture, where every team member is celebrated, respected, and has their voice heard, our comprehensive benefits package includes:
<ul>
<li>$90,000 to $94,000 per annum, depending on your previous experience, as well as a discretionary profit share bonus paid twice per year. Please note that we have established salary bands that ensures a fair and consistent approach for all applicants, eliminating the need for individual negotiations</li>
<li>23 days’ vacation leave increasing by 1 day each year to a maximum of 27 days. 6 public holidays plus 1 floating vacation day to use on a holiday of your choosing</li>
<li>Flexible working hours and the chance to work from home for up to half of your working time</li>
<li>Private medical insurance with a company contribution, as well as dental and vision cover, and life insurance</li>
<li>Retirement savings via a 401k plan with up to a 5% employer match</li>
<li>Paid funding for external education, and study leave</li>
<li>Paid and unpaid sabbaticals based on length of service</li>
<li>Regular company-funded social activities </li>
</ul>
Please click here to learn about our reward package and the other benefits of working for Costello Medical: <a href="https://www.costellomedical.com/careers/benefits-package-in-the-us/" target="_blank">https://www.costellomedical.com/careers/benefits-package-in-the-us/</a> 
<h3> The Application Process</h3>
You are required to submit your resume and a cover letter via our online application form. In your cover letter, you must explain why you think you would be suited to the role and why you would like to join Costello Medical, with examples to support both. Your resume should clearly state the dates of all qualifications and grades achieved where applicable.
Our recruitment process includes a telephone call with a member of the Talent Acquisition team, followed by a written assessment and proofreading exercise for you to complete in your own time. If successful, you will be invited to an interview which will include a short presentation that you can prepare for in advance. Our standard recruitment process lasts around 1 month, however, this is adapted if necessary. 
As an equal opportunity employer, we are committed to fostering a diverse and inclusive workforce and, throughout the recruitment process, there are a number of reasonable adjustments we can provide. Please <a href="https://www.costellomedical.com/reasonable-adjustments/" target="_blank">click here</a> to learn more.
Please note that, whilst we embrace AI to innovate and improve processes, your role may involve confidential data that cannot be uploaded to AI. Therefore, it is important for us to assess your own skills and abilities, so we recommend that you do not rely solely on this technology to generate any application materials.
<h3> Visa Sponsorship</h3>
We welcome applications from international candidates, but we cannot provide visa sponsorship for working visas. Therefore, you must have the right to work in the US independently from the company. However, we do consider those on a temporary visa, such as an OPT visa.

Senior Medical Writer

<h3>Job Description</h3>
Job Description
???? Location: Bothell, WA • Cambridge, MA • Plymouth, MN (Hybrid – 3 days onsite)
Are you a clinical science expert ready to impact the future of ultrasound technology? Join our innovative team as a Senior Clinical Development Scientist and lead the strategy, execution, and documentation of clinical studies that drive regulatory success and patient outcomes.
???? Key Responsibilities:
<ul>
<li>
Design and lead clinical studies (pre-market and post-market) for ultrasound products.
</li>
<li>
Develop protocols, CSRs, CERs, and regulatory documentation to support FDA and international submissions.
</li>
<li>
Collaborate with cross-functional teams (R&amp;D, Regulatory, Medical Affairs, Market Access).
</li>
<li>
Engage with investigators, IRBs, and global regulatory agencies (FDA, EMA, NMPA).
</li>
<li>
Analyze clinical data, support health economics evidence, and drive publication strategy.
</li>
</ul>
???? Ideal Candidate Has:
<ul>
<li>
PhD or MD in a relevant scientific field (required).
</li>
<li>
7+ years in clinical research or development, preferably with medical devices.
</li>
<li>
Strong experience designing clinical studies for regulatory environments (FDA, EU-MDR).
</li>
<li>
Solid understanding of GCP, design controls, and product development processes.
</li>
<li>
Excellent writing and communication skills in English for scientific documentation.
</li>
<li>
Experience with ultrasound and/or AI-driven clinical validation (a plus).
</li>
<li>
Based near one of the required offices with ability to work onsite 3 days/week.
</li>
</ul>
???? Why Join Us?
<ul>
<li>
Help shape the next generation of ultrasound innovation.
</li>
<li>
Collaborate with thought leaders and make an impact globally.
</li>
<li>
Competitive salary, benefits, and opportunities for growth.
</li>
</ul>

Senior Clinical Development Scientist (Ultras

Currently, we do not have specific job openings available. However, we are eager to connect with professionals who are interested in future opportunities with our organization. We encourage you to submit your resume so that we can consider you when roles aligned with your expertise and interests become available.
Requirements
If you are interested in future opportunities, please submit your resume. 
Your information will be kept in our talent pool, and we will reach out to you should a suitable position arise.
Benefits
<ul>
<li>Health Care Plan (Medical, Dental &amp; Vision)</li>
<li>Retirement Plan (401k with the company match)</li>
<li>Life Insurance (Basic, Voluntary &amp; AD&amp;D)</li>
<li>Unlimited Paid Time Off Policy</li>
<li>Family Leave (12 weeks for primary caregiver/ birthing parent, 3 weeks for non-primary caregiver)</li>
<li>Short Term &amp; Long-Term Disability</li>
<li>Training &amp; Development</li>
<li>Hybrid Work Setting</li>
<li>Free Snacks and Company Lunches on Wednesdays</li>
<li>Wellness Resources</li>
<li>Stock Option Plan</li>
<li>Foghorn Therapeutics is pleased to provide you and your family with a comprehensive suite of benefits, including:</li>
<ul>
<li>Highly competitive and inclusive medical, dental and vision coverage options</li>
<ul>
<li>BCBS PPO and PPO HSA plans</li>
<li>BCBS Dental Plan</li>
<li>EyeMed Vision Plan</li>
</ul>
<li>FSA and HSA for medical expenses and dependent care expenses</li>
<li>401(k) Program via Fidelity with the company match</li>
<li>Corporate Wellness Program</li>
<li>Unlimited Paid Time Off policy</li>
<li>Winter shut down</li>
<li>12 weeks of 100% paid parental leave for birthing/primary parent and primary guardian in case of adoption and 3 weeks of 100% paid parental leave for non-birthing/non-primary parent/guardian.</li>
<li>Paid Life, LTD and STD insurance coverages, as well as voluntary benefit options</li>
<li>Free parking, subsidized commuter passes, or a $100 monthly stipend for walking/biking to work</li>
<li>Company lunches on Wednesdays</li>
</ul>
<li>Foghorn Therapeutics is a smoke-free, alcohol-free and drug-free work environment. </li>
<li>Foghorn is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. Foghorn Therapeutics will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.</li>
</ul>

Future Opportunities

Cambridge Isotope Laboratories, Inc. (CIL) is searching for a&nbsp;Senior Chemist I based onsite in our Andover, MA facility.&nbsp; CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets.&nbsp; CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years.
The Senior Chemist I will be responsible for the de novo synthesis, route development, and final product characterization of a wide variety of complex isotopically labeled targets (13C, 15N, 18O, and D isotopes). This role demands the production of high-quality, finished products in accordance with established specifications, while adhering to CIL’s safety and general policies. The Senior Chemist I will operate with a high degree of autonomy, ensuring that production requirements for safety, yield, time, and quality are consistently met.
Responsibilities 
<ul>
<li>Adhere to CIL’s general and safety policies to maintain a safe work environment</li>
<li>Synthesize complex, non-routine, and routine target compounds containing isotopes such as 15N, 18O, D, and/or 13C, utilizing established SOPs where applicable</li>
<li>Design and develop new synthetic routes when required to achieve optimal results</li>
<li>Contribute to the optimization of chemical processes for targeted molecules, intermediates, and scalable, cost-effective production methods</li>
<li>Analyze and interpret data using various techniques, including Nuclear Magnetic Resonance (NMR), Ultraviolet (UV) Spectroscopy, Mass Spectrometry (MS), High-Performance Liquid Chromatography (HPLC), and Infrared (IR) Spectroscopy</li>
<li>Employ a variety of purification techniques, including chromatography, distillation, recrystallization, and sublimation</li>
<li>Maintain accurate and detailed records in the laboratory notebook</li>
<li>Mentor and assist junior team members, offering guidance on experimental techniques and troubleshooting</li>
<li>Ensure all work is conducted with strict adherence to safety protocols and good laboratory practices, in line with CIL’s safety manual</li>
<li>Perform additional related duties as needed</li>
</ul>
Requirements
<ul>
<li>Ph.D. in Synthetic Organic Chemistry or a closely related field, or a Master's degree with significant relevant experience (e.g., 5+ years in organic chemistry and/or synthesis)</li>
<li>Alternatively, a Bachelor's degree in Chemistry or a related field with extensive hands-on experience in organic synthesis and chemical processes may be considered</li>
<li>1-3 years of professional experience in organic chemistry and/or synthesis, or equivalent practical training as a Research Assistant or Postdoctoral Researcher</li>
<li>Expertise in organic synthetic methods, chemical separation, and compound identification, with strong analytical skills</li>
<li>Proficiency in laboratory techniques, including synthesis, purification, and characterization of organic compounds</li>
<li>Excellent verbal and written communication skills. Additionally, strong documentation and collaboration skills are essential</li>
<li>Ability to perform hands-on bench chemistry, which may involve standing, bending, and stooping</li>
<li>Familiarity with working in a controlled, hooded lab environment, as required by safety protocols</li>
<li>Comfortable working with both hazardous and non-hazardous chemicals</li>
<li>Physical ability to lift 50 lbs regularly and transport drums of chemicals, including up to 55-gallon drums, using appropriate equipment (e.g., drum dolly)</li>
</ul>
Benefits
CIL and CIS offer a competitive salary and comprehensive benefits including generous paid time off, Long Term Incentives, 6% matching 401K plan and health insurance with no in-network deductible.
Cambridge Isotope Laboratories is an Equal Opportunity Employer. 
Learn more about us on our website:&nbsp;<a href="http://www.isotope.com/" target="_blank">www.isotope.com</a>
About Us: Cambridge Isotope Laboratories, Inc. (CIL) is the world’s leading producer of&nbsp;<a href="http://www.isotope.com/userfiles/files/assetLibrary/MET_MATTHEWS.pdf" target="_blank">stable isotopes&nbsp;</a>and stable isotope-labeled compounds. With approximately 750 employees and laboratories in four countries, CIL specializes in the process of labeling biochemical and organic compounds with highly enriched, stable (nonradioactive) isotopes of carbon, hydrogen, nitrogen and oxygen. Our chemists substitute common atoms (e.g., 1H, 12C, 14N, 16O) with rare, highly valued isotopes (e.g., 2H or D, 13C, 15N, 18O) so that the final product can be readily measured or traced using mass spectrometry (MS) or nuclear magnetic resonance (NMR). CIL’s products are utilized in laboratories, medical, government and academic research centers and health care facilities worldwide.
We are proud that CIL products have contributed to medical advancements in cancer research, new-drug development, environmental analysis, and medical diagnostic research. In the past decade, as the fields of proteomics and metabolomics have developed as leading techniques for determining biomarkers for disease presence, progression and the monitoring of therapeutic response, CIL has worked closely with industry leaders and researchers to provide the stable isotope-labeled tools needed for improved quantitation and qualification of complex biological systems.
After decades of research, stable isotopes have found their place in an ever expanding commercial scale applications in pharmaceuticals, semiconductors, flat panel displays as well as other high technology fields specifically with deuterium oxide (D2O) and deuterium gases. Pharmaceutical companies have begun to investigate deuteration of molecules that may provide advantages over their existing nondeuterated counterparts. In addition, increasing research into the potential medical advantages of new deuterated drugs is also occurring. In high technology, deuterated organic molecules and deuterium gas are commonly used in the manufacturing of microelectronics and OLEDs, which contribute to the increased lifetime of the devices.
Learn more about us on our website:&nbsp;<a href="http://www.isotope.com/" target="_blank">www.isotope.com</a>

Senior Chemist I

<h3>Job Description</h3>
Baystate Health is a not-for-profit, integrated healthcare system in western Massachusetts which consists of an academic medical center, Baystate Children’s Hospital, three community hospitals and the region’s largest multispecialty group.&nbsp; Our flagship hospital, Baystate Medical Center, is home to the University of Massachusetts Chan Medical School-Baystate.&nbsp;
POSITION HIGHLIGHTS:
<ul>
<li>Provide clinical and academic leadership of our well-established Division of Medical Genetics at Baystate Medical Center. Lead our experienced team of one physician, one APP, five genetic counselors, a care coordinator and a MA.&nbsp;</li>
<li>Housed in the Dept. of Pediatrics, our diverse team provides genetics care for patients across the lifespan. The program includes pediatric genetics, reproductive genetics and genetic counseling, cancer genetics and genetic counseling (Family Cancer Risk program), adult genetics, and our nationally recognized lysosomal storage disorders program.</li>
<li>Direct operations for our inpatient consult service as well as ambulatory service at nearby Baystate Children’s Specialty Center. This position offers 0.3 FTE administrative time.</li>
<li>Support faculty/team development and contribute to the department’s and hospital’s strategic vision and mission.</li>
<li>Faculty appointment at UMass Chan Medical School- Baystate (preferably Associate Professor or higher). Foster an environment of educational excellence through direction of our resident elective and lecturing to residents and med students.</li>
<li>Qualifications:
<ul>
<li>ABMS board certification in Medical Genetics</li>
<li>4+ years of experience post-training with interest in management and leadership.</li>
<li>Strong track record of interdisciplinary collaboration; excellent interpersonal and communication skills, enthusiasm for medical education and mentoring residents, and ability to engage a broad base of stakeholders.</li>
</ul>
</li>
</ul>
THE ADVANTAGES OF WORKING WITH BAYSTATE:

<ul>
<li>Compensation plan includes base salary and opportunity to earn incentive bonuses</li>
<li>Robust relocation package</li>
<li>Flexibility- opportunities to flex your FTE to fit your life</li>
<li>Immediate access to paid time off</li>
<li>Lucrative 403b match and 457b plan</li>
<li>Professional development and mentorship</li>
<li>Wellbeing programs that include mental, physical, and financial health and more</li>
</ul>
For more information please contact:
Ruben Vaidya, MD, Division Chief of Newborn Medicine
C/O Melissa Hale, Senior Provider Recruiter
<a href="mailto:Melissa.Hale@baystatehealth.org" target="_blank">Melissa.Hale@baystatehealth.org</a> or 413-794-2624

Genetics, Division Chief, Medical Genetics

<h3>Role Summary </h3>
<ul>
<li> Responsibilities: You will be given hands-on experience working across Medical Communications, Evidence Development and/or Value and Access projects, all of which involve the assimilation, interpretation and creative presentation of scientific data related to pharmaceuticals or medical devices</li>
<li> Compensation: $24 to $30 per hour depending on experience</li>
<li> Benefits: Generous vacation leave allowance, flexible working hours and the chance to work from home 1 day per week, access to medical, dental and vision insurance, as well as funded social activities</li>
<li> Role Type: Full-time, 3-month internship</li>
<li> Start Date: We are currently recruiting for start dates in September and you will be asked to state your availability on your application form</li>
<li> Location: This role is available in our <a href="https://www.costellomedical.com/careers/locations/working-in-boston/" target="_blank">Boston</a> office</li>
</ul>
<h3> About the Role </h3>
Our internships are ideal for current students and recent graduates in the sciences seeking to gain an insight into life at a fast-growing healthcare consultancy. We work with a wide range of clients, including the industry’s most successful pharmaceutical and medical technology companies, patient and public health organizations and non-profits. You will gain hands-on experience with a variety of projects, typically working on two to three projects for the duration of your internship. All projects involve the assimilation, interpretation and creative presentation of data from clinical trials, and depending on your team and project allocations, you could be working on anything from medical communications to market access and evidence synthesis. Specific tasks could include supporting the preparation of medical education slides, performing systematic searches of medical literature, developing clinical trial manuscripts, or assimilating clinical and cost-effectiveness evidence to support HTA submissions to NICE. These meaningful and exciting projects contribute to improving healthcare outcomes globally. Interns receive one-to-one training on the technical aspects of the role and learn about project management and effective communication with clients.
Analyst/Medical Writer Interns may be based in any of our scientific teams, and while you are here you would likely be working across projects for two different teams. Whether you are hired as an Analyst Intern or Medical Writer Intern will be determined by which team you are based in, though the responsibilities of the role are quite similar regardless of your team allocation. Generally, only applicants who will be working in Publications have the job title of Medical Writer Intern. These are broadly categorized as <a href="https://www.costellomedical.com/what-we-do/medical-communications/" target="_blank">Medical Communications</a>, <a href="https://www.costellomedical.com/what-we-do/value-and-access/" target="_blank">Value and Access</a>, <a href="https://www.costellomedical.com/what-we-do/evidence-development/" target="_blank">Evidence Development,</a> and <a href="https://www.costellomedical.com/what-we-do/rare-diseases/" target="_blank">Rare Diseases</a>. If you have a particular interest in any of our services, please indicate this in your cover letter. Please note that, if successful, your team will be confirmed closer to your start date and, while every effort will be made to consider your team preference, this will be subject to business need and project availability.
Hybrid Working Policy: We recognize that home-working can improve work life balance, reduce commuting times and costs, and provide the opportunity to juggle personal commitments. At the same time, we believe that having face-to-face time in the office holds many benefits and is central to ensuring that the community we have created, where people have a workplace they belong to and feel part of, is never lost. Given the wealth of training, mentorship and development opportunities that are available as part of our internship programs, time spent in the office is even more crucial. Therefore, our Interns are able to work from home for 1 day per week. 

<h3>A Day in the Life of an Analyst/Medical Writer Intern</h3>
<a href="https://www.costellomedical.com/day-in-the-life/scientific-intern.html" target="_blank"></a>To learn more about a typical day for an Analyst/Medical Writer Intern at Costello Medical, please click here: <a href="https://www.costellomedical.com/day-in-the-life/scientific-intern.html" target="_blank">https://www.costellomedical.com/day-in-the-life/scientific-intern.html</a>
<h3>Career Prospects After the Internship</h3>
<a href="https://www.costellomedical.com/careers/working-at-costello-medical/" target="_blank"></a>During the internship program, individuals performing well may be given the opportunity to extend their internship to six months (note that this is dependent on business need. When this happens, it allows our interns to further develop their skills and potentially gain experience of other areas of the company (again, dependent on business need as well as the individual’s interests). Additionally, there is the opportunity for strong candidates to apply for the Analyst/Medical Writer role and join our expanding team on a permanent basis. On average, 34% of our UK Analyst/Medical Writer Interns move into a permanent role with Costello Medical. We are hopeful that a similar percentage or more will progress into permanent roles in this new US internship program. To learn more about the benefits that we offer for permanent roles, please click here: <a href="https://www.costellomedical.com/careers/working-at-costello-medical/benefits-package-in-the-us/" target="_blank">https://www.costellomedical.com/careers/working-at-costello-medical/benefits-package-in-the-us/</a> 
To learn more about the personal and professional development we offer at Costello Medical, please click below to read firsthand accounts from our colleagues about their time with the company: <a href="https://www.costellomedical.com/careers/working-at-costello-medical/" target="_blank">https://www.costellomedical.com/careers/working-at-costello-medical/</a> 
Requirements
<h3>About You</h3>
This internship is suited to recent graduates and post-graduates, as well as current students who are permitted to complete full time internships either during the holidays or as a placement as a part of their degree. Please note that we do not recommend completing the Analyst/Medical Writer Internship program at the same time as studying, completing a dissertation or writing a PhD thesis due to the competing demands of your workload in your course and the role.
Essential requirements for the role are:
<ul>
<li> A degree or enrolled in a degree program in a scientific discipline (minimum or expected GPA 3.3). We welcome applications from candidates with a diverse range of educational backgrounds, but particularly those with coursework in the life sciences</li>
<li>Exceptional attention to detail</li>
<li>Strong analytical skills</li>
<li>Excellent written English and spoken English, and the ability to communicate scientific material clearly in both written and oral form for a variety of audiences</li>
<li>Strong organizational skills and the ability to plan your own work effectively, with a proactive approach to task prioritization and time management</li>
<li>The ability to communicate effectively and work collaboratively as part of a team</li>
<li>Strong self-motivation, self-awareness and willingness to learn, with a desire to contribute to the company above and beyond project work </li>
<li>Fluency in Microsoft Word, Excel and PowerPoint</li>
<li>A genuine interest in healthcare and an eagerness to learn about new areas of science</li>
</ul>

<h3>About Costello Medical </h3>
Costello Medical is a rapidly growing global healthcare agency specializing in medical communications, market access and health economic and outcomes research. We work with a wide range of clients, including the industry’s most successful pharmaceutical and medical technology companies, patient and public health bodies and charitable organizations. Our mission is to be a community of the very best people, building trusted partnerships across the healthcare sector by delivering an exceptional service. Our vision is to be a leading global partner consistently striving for meaningful and outstanding contributions that improve people’s health and lives.
On May 27th 2022 Costello Medical received its certification as a <a href="https://www.bcorporation.net/en-us/find-a-b-corp/company/costello-medical-consulting-ltd" target="_blank">B Corporation</a>. We are really proud of this achievement as it demonstrates that Costello Medical is meeting the highest standards of verified social and environmental performance. We underwent a rigorous assessment that covered the whole of our business including employee benefits, charitable giving and sustainability. We believe this certification is external validation of our mission to be a force for good.
<h3>The Recruitment Process </h3>
Our recruitment process includes a written assessment and proofreading exercise for you to complete in your own time. If successful, you will be invited to an interview with our members of our Analyst/Medical Writer recruitment team. Our standard recruitment process lasts around 1 month, however, this can be adapted if necessary.
As an equal opportunity employer, we are committed to fostering a diverse and inclusive workforce and, throughout the recruitment process, there are a number of reasonable adjustments we can provide. Please <a href="https://www.costellomedical.com/reasonable-adjustments/" target="_blank">click here</a> to read more about this and contact the People team via <a href="mailto:recruitment@costellomedical.com" target="_blank">recruitment@costellomedical.com</a> should you require reasonable adjustments at any stage.
We are currently recruiting for start dates in September and you will be asked to state your availability on your application form. 
While there are no set application deadlines, we strongly recommend applying as early as possible so that we can begin processing your application. The role will close when suitable candidates are found. 
Please note that this role is available in our&nbsp;Boston office, which you can learn more about here: <a href="http://www.costellomedical.com/careers/locations" target="_blank">www.costellomedical.com/careers/locations</a> 
Benefits
<h3>What We Offer </h3>
We offer a competitive hourly rate of $24 to $30 per hour, depending on experience, and you will be entitled to pro-rated vacation days, based on internship length.&nbsp;We are proud to be a certified B Corporation company as this certification is a testament to the exceptional team at Costello Medical and their steadfast commitment to being a force for good. We are therefore eager to welcome individuals who share this vision. We provide exceptional internal training, opportunities to work on pro bono and charitable projects, and regular company-funded social activities.
<h3>How to Apply </h3>
You are required to submit your resume and a cover letter via our online application form. In your cover letter, you must explain why you think you would be suited to the role and why you would like to join Costello Medical, with examples to support both. Your resume should clearly state the dates of all qualifications and grades achieved where applicable.
While we embrace Artificial Intelligence (AI) technologies to innovate and improve processes, we want to understand your unique skills and experiences throughout the recruitment process. Therefore, if you use AI to assist with your application, we recommend that you do not rely solely on this technology to generate your application materials. As your role may involve developing new written content from scratch and handling confidential data that cannot be uploaded to AI technology, it is important for us to assess your own skills and abilities.
Please contact the Talent Acquisition team at <a href="mailto:recruitment@costellomedical.com" target="_blank">recruitment@costellomedical.com</a> if you have any questions about the role or application process.
<h3>Visa Sponsorship </h3>
We welcome applications from international candidates, but we are unfortunately unable to provide visa sponsorship for working visas. Therefore, you must have the right to work in the US independently from the company. However, we are able to consider those on a temporary visa, such as an OPT visa.

Analyst/Medical Writer Internship

<h3>Job Description</h3>
Job DescriptionOur client in Westwood MA is seeking a Chemist to join the team Duties: - Prepare and test samples by performing physical, chemical, and electrical evaluations on both new and existing products in accordance with specified standards. - Operate, calibrate, and maintain analytical instruments, including FTIR, TGA, DSC, TMA, GC/MS, and GPC. - Conduct analysis of raw materials and final products to ensure compliance with quality specifications. - Manage inventory of essential lab consumables and critical spare parts to ensure uninterrupted operation of analytical equipment. - Develop and validate reliable testing methodologies for the analysis of raw materials and finished products. - Train laboratory technicians in established analytical procedures to ensure consistency and accuracy. Requirements: - BS or MS degree in chemistry, polymer science or a related field with three or more years of laboratory experience - High school diploma or equivalent acceptable with 10+ years laboratory experience - Successful candidate should have demonstrated experience with the following instruments / techniques: FTIR, TGA, DSC, TMA, GC/MS, GPC, HPLC. - Experience in set up, calibration, maintenance, methods development / optimization, interpretation and reporting of results required. - Excellent communication skills required. Ability to organize and present scientific data to technical and non-technical audiences. - Strong organizational skills with ability to execute multiple parallel projects #ZRPB

Chemist

<h3>Job Description</h3>
Job Description
Description:
<ul>
<li>
Responsible for conducting an independent research project under the co-mentorship and supervision of research scientists.
</li>
<li>
Attend on-boarding and training sessions
</li>
<li>
Plan, design, and execute a research project as agreed upon your scientist co-mentors (aka "Supervisors")
</li>
<li>
Actively participate in weekly Summer Internship Program professional development sessions/workshops
</li>
<li>
Present research project at an end of program poster session
</li>
<li>
Adhere to all policies
</li>
</ul>
QUALIFICATIONS:
<ul>
<li>
Enrolled in a US academic institution and have completed at least 3 semesters
</li>
<li>
Have a GPA of at least 3.0 on a 4.0 scale
</li>
<li>
Have a strong desire to pursue a graduate-level STEM degree for biomedical research
</li>
</ul>
Benefits:
Healthcare Insurance: Synectics offers eligible employees and their dependents healthcare coverage through BlueCross BlueShield of Illinois. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. Premiums are subsidized by Synectics. 
Dental Insurance: Synectics offers eligible employees and their dependents a dental plan through MetLife. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics. 
Vision Insurance: Synectics offers eligible employees vision insurance through VSP. Eligibility begins on the 1st day of the calendar month following 60 days of continuous full time employment with Synectics.401(k) Plan: The Synectics Inc. Investment Savings Retirement Plan. Synectics offers all employees who are 21 years of age or older the opportunity to invest in the 401(k) Plan on the first enrollment date that is at least 30 days after employment begins. Enrollment dates are each January 1st, April 1st, July 1st, and October 1st.
Technical Certification Bonus: Synectics is pleased to award its employees a bonus of up to $500 for an approved professional certification. In determining the bonus amount, Synectics will consider the cost of the test(s) for any certification relating to your current position, achieved during your employment with us. Only one Certification Bonus per calendar year may be awarded per employee. Only current, active employees will be eligible to receive this bonus. It will be awarded 90 days after the Synectics office has received documentation confirming the successful completion of the certification.
Synectics is an equal opportunity employer.

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