Regulatory and Start Up Specialist

Precision for Medicine(6 days ago)

United StatesOnsiteFull TimeMedior$68,700 - $103,100Regulatory Affairs

About this role

The Regulatory and Start Up Specialist (RSS) is an experienced professional responsible for managing regulatory and site start-up activities for clinical trials. This role involves coordinating submissions, ensuring compliance, and supporting site activation and collaboration to facilitate efficient trial conduct.

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Required Skills

Regulatory Affairs
Clinical Trials
IRB
ICH-GCP
Document Management
Languages
Project Management
Submission
Site Activation
Contracts

About Precision for Medicine

precisionformedicine.com

Precision 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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