Clinical Study Start Up Lead

Clinical Study Start Up Lead South San Francisco, United States | Posted on 05/05/2026 Job Duration: LongTerm Contract (Possibility Of Extension) Pay Rate : $90/hr on W2 We are seeking a ClinicalStudy Start-Up professional to drive the efficient and compliant initiation of clinical trials . This role leads country-level start-up strategy, regulatory submissions, and site activation while ensuring alignment with global timelines and standards. You will collaborate with cross-functional teams, CROs, and regulatory bodies to enable seamless clinical trial execution. Key Responsibilities: Lead country start-up strategy and execution for clinical trials Oversee site activation, regulatory submissions, and amendments Ensure compliance with ICH-GCP, EU CTR, and local regulations Manage ICF processes, site documentation, and trial materials Coordinate with CROs, investigators, and regulatory authorities Drive process improvements, automation, and standardization Manage budgets, contracts, and payment oversight Support cross-functional alignment with global and regional teams Qualifications: Degree in Life Sciences (Bachelor’s required; advanced degree preferred) 2–6+ years of experience in clinical trial start-up / clinical operations Strong knowledge of regulatory submissions and study start-up processes Experience with clinical systems (Veeva Vault, CTIS, RIM, etc.) Experience working with CROs and external vendors Key Skills: Strong communication, stakeholder management, and collaboration Excellent organizational, analytical, and problem-solving skills Ability to manage multiple priorities in a global, matrixed environment Detail-oriented with a focus on compliance and timelines #J-18808-Ljbffr