Sr Clinical Trials Management Associate

R&D Partners is seeking to hire a Sr Clinical Trials Management Associate in Los Angeles.

Your main responsibilities as a Sr Clinical Trials Management Associate:

• Conduct site evaluation, site initiation, routine monitoring and closeout visits as required
• Assure site compliance with routine protocol and regulatory requirements and quality of data
• Draft and coordinate review of protocols, informed consents, case report forms and monitoring plans
• Assist in the review of routine data and preparation of safety, interim, and final study reports, and resolution of data discrepancies
• Participate or effectively run meetings with CROs, vendors, and multi-functional teams

What we are looking for in a Sr Clinical Trials Management Associate:

• BS/BA in Life Sciences with 4+ years of biopharma experience
• Working knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of routine clinical trials
• Demonstrated experience with prioritizing multiple tasks, planning proactively, and meeting goals using well-defined instructions and procedures

Why choose R&D Partners?
As an employee, you have access to a comprehensive benefits package including:

• Medical insurance – PPO, HMO & HSA
• Dental & Vision insurance
• 401k plan
• Employee Assistance Program
• Long-term disability
• Weekly payroll
• Expense reimbursement
• Online timecard approval

Salary:

• $125,000 – $139,360 (Dependent on Experience)

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners is acting as an Employment Agency in relation to this vacancy.

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