Regulatory and Start Up Specialist
Precision for Medicine(1 day ago)
About this role
Precision for Medicine is seeking a Regulatory and Start Up Specialist to join their team. The role involves managing site activation processes for clinical trials, including documentation, regulatory submissions, and coordination with sites and regulatory authorities.
Required Skills
- Regulatory Submissions
- Clinical Trials
- Documentation
- IRB/Ethics
- Project Management
- Regulatory Affairs
- Site Activation
- Translation
- Compliance
- Biomarker
Qualifications
- Bachelor’s degree in life sciences or related field
- 1 year or more experience in regulatory or start-up roles
About Precision for Medicine
precisionformedicine.comPrecision for Medicine is a global clinical research organization (CRO) that uses advanced technologies and translational science to maximize insights into patient biology and inform drug development. They offer integrated services—including biomarker strategy, bioanalysis, multi‑omics and data analytics—alongside clinical trial design and execution to support precision medicine programs. Their platform-driven approach helps sponsors improve patient selection, de‑risk development, and accelerate timelines across therapeutic areas. Precision for Medicine partners with biotech and pharma to move candidates from early development toward approval.
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