Sign up with

Already have an account? Log in here

Need some help?
Talk to us at +91 7670800001

Clinical Study Start Up Lead at Dawar Consulting, Inc.

South San Francisco, California, United States -

Full Time

Start Date

Immediate

Expiry Date

03 Aug, 26

Salary

90.0

Posted On

05 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Communication, Stakeholder Management, Collaboration, Organizational Skills, Analytical Skills, Problem-solving, Compliance Management, Timeline Management

Industry

IT Services and IT Consulting

Description

Our client, a world leader in diagnostics and biotechnology, is looking for a "Clinical Study Start Up Lead” based out of South San Francisco, CA. Job Duration: Long Term Contract (Possibility Of Extension) Pay Rate : $90/hr on W2 We are seeking a Clinical Study 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 If interested, please send us your updated resume at hr@dawarconsulting.com/akansha@dawarconsulting.com

Responsibilities

Lead country-level start-up strategy, regulatory submissions, and site activation for clinical trials. Coordinate with CROs and regulatory bodies to ensure compliant and efficient trial execution.