Clinical Contracts Associate

Job Description

Job Description

We are a national staffing firm and are currently seeking a Clinical Contracts Associate for a prominent client of ours in Foster City, CA. Hybrid , on site 3 days a week. Details of the position are as follows: 

 

Job Details:

• Pay Rate: $40 – $42.74 hr.
• 1 year assignment, possibility of extension or conversion.
• Monday – Friday, 8AM – 5 PM.
• Looking for a Clinical Contracts Associate (Vendor Qualification Associate I), who will report to the Director of Vendor Outsourcing. The candidate will be responsible for ensuring high quality of data and services across all vendors supporting global R&D portfolio – Ph I-IV clinical trials.
• The candidate should have a deep understanding of vendor capability assessments, sourcing, contracting, procurement, category management, and inspection readiness activities as they will be leading and/or supporting those cross-functional efforts.
• The candidate should also have an understanding of various clinical trial activities such as clinical monitoring, data management, Real World Data/Evidence (RWD/RWE), biostatistics, medical writing, Ph 1 CRU, central lab, biomarker lab, bioanalytical lab, RTSM, eCOA, medical imaging, safety, e-informed consent, mobile HCP services, telemedicine and wearables/sensors.
• Daily activities will include, but are not limited to, conducting Request for Information (RFI), Data Privacy and Security IT Assessments, Anti-Bribery and Anti-Corruption Due Diligence, Financial Health Assessments, Inspection Readiness Preparation Activities, Data Analyses and Benchmarking to Provide Data Informed Insights into Strategies and Continuous Improvement Initiatives, Presentations, and Trainings.

 

Qualifications:

• BS or BA with 5 years of relevant experience. PMP certification or equivalent certification.
• The candidate should have executive presence, excellent communication skills, project management & critical thinking skills; comfortable interacting with internal stakeholders and external vendors.
• Will be regularly partnering with team members such as R&D Quality & Compliance, clinical operations, finance, legal, business conduct, vendor relationship management, payments, and vendors.
• Expected to complete tasks and projects under minimal supervision and has the ability to manage competing priorities effectively and proficiently.
• Demonstrates a thorough knowledge of Good Clinical Practice “GCP”, Good Pharmacovigilance