The Opportunity

We're looking for a Clinical Contracts Associate II, working in the Biotechnology/Medical Devices industry in Foster City, California, United States.

  • Lead vendor qualifications in the clinical outsourcing of global Phase I-IV clinical trials, which may include clinical monitoring, data management, biostatistics, medical writing, Phase 1 CRU, central lab, biomarker lab, bioanalytical lab, RTSM, eCOA, medical imaging, safety, e-informed consent, mobile HCP services, telemedicine and wearables/sensors.
  • Assist with other vendor assessments in the Development Business Operations group (i.e., IT Security Assessments, Anti-Bribery and Anti-Corruption Due Diligence, etc.).
  • Manage the entire life cycle of vendor qualification, comprised of vendor pre-qualifications and vendor re-qualifications.
  • Work with Vendor Outsourcing Managers, Vendor Selection Teams and internal customers in the vendor qualification process and may assist with the planning of vendor capabilities presentations during the vendor bid defense meetings.
Details

We are offering Competitive Compensation and Benefits. This position may present an opportunity to go permanent.

Our Client

Our client is a people driven staffing company.  Growing fast - 33% annually! 

How?  Building trusting relationships with top candidates. Like you!  You’ll get one-on-one time focused on your skills, needs, and discovering opportunities in which you’ll thrive.  The goal is to place you in the right position for you and your goals. 

Where?  Top IT and telecommunications companies.  You’ll make a difference and grow in Technology, Government Services, Professional Services, or Engineering.

Helping you achieve your goals!  It’s the right way and the only way to succeed in staffing.

Experience Required for Your Success
  • BS or BA with 8+ years of relevant experience
  • Candidate has 10+ years of relevant experience in the pharmaceutical or bio-pharmaceutical industry
  • Demonstrates a thorough knowledge of Good Clinical Practice GCP, Good Pharmacovigilance Practices GVP, Good Laboratory Practice GLP
  • Good Documentation Practice GDP and ICH E6 R2 compliance requirements
  • Demonstrates a thorough understanding of current global and regional trends in compliance
What Do You Think?

Does your experience reflect what it takes to be successful in this role? Do the work and challenges get you excited about what's possible? Apply here.

Not exactly? Join Our Talent Community, and we'll let you know of additional opportunities.

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