CLINICAL TRIAL ASSOCIATE (CTA)

SCOPE

Exciting opportunity to join a growing Clinical Operations team supporting multi-phase clinical trials. Offering room for growth and above-market salary, this role is an excellent opportunity in a stable, mid-size biopharma company in Southern California. As a Clinical Trial Associate, you will be providing comprehensive support to Senior Executives and Clinical Operations teams.

RESPONSIBILITIES

• Maintain trial master file and regularly perform quality check on all documents and data for completeness and accuracy
• Maintain study trackers across multiple clinical sites
• Assemble regulatory binders, study reference manuals, and study supplies for distribution.
• Support planning and coordination of site visits and CRA trainings
• Coordinate with CROs and study vendors
• Ensure compliance with study-specific processes, SOPs, ICH/GCP and industry regulations

EDUCATION/EXPERIENCE

• Bachelor’s Degree in life sciences or equivalent required
• 1+ years relevant experience in life sciences or pharmaceutical company required
• Previous experience in oncology clinical trials strongly preferred
• Demonstrated knowledge of industry regulatory requirements, including ICH/GCP and clinical trial operations guidelines
• Travel may be required (up to 20%)

SKILLS:

• Excellent verbal and written communication skills
• Database proficiency, including eTMF

My team and I are working on a number of additional opportunities for a broad portfolio of clients across the US and internationally. If this role isn't for you but you would like to explore your options in the market, I would welcome a confidential conversation at your convenience. Please contact me at (619) 350-6149 or e.mato@hamlynwilliams.com.