Job Description
Overview:
This role will drive policies, procedures, governance frameworks, and cross-functional execution for disclosure of clinical trial information, results, and patient-level data-sharing, positioning as a leader in data transparency and accountability.
Qualifications
- Advanced degree in life sciences, public health, or related field (PhD, PharmD, or equivalent strongly preferred).
- 8-10 years of industry experience in regulatory affairs, clinical research, medical writing, or related areas, with 5 years in clinical trial disclosure and transparency.
- Demonstrated expertise in global disclosure regulations (FDA/ClinicalTrials.gov, EU CTR, EudraCT, EMA Policy 0070, Health Canada PRCI, Japan PMDA, WHO).
- Proven track record of building and leading global teams and/or major transparency initiatives.
- Strong understanding of clinical development, regulatory submissions, and data privacy principles.
- Exceptional leadership, communication, and collaboration skills.