Clinical Contracts Associate II - Hybrid

Up to US$42 per hour + Highly Competitive Salary
  1. Contract
  2. Clinical Scientist, Clinical Outsourcing, Clinical Evaluation
  3. United States
Santa Monica, USA
Posting date: 21 Dec 2022
CR.KC.50086

This vacancy has now expired. Please see similar roles below...

Proclinical is seeking a hybrid Clinical Contracts Associate for a leading biopharmaceutical organization located in Santa Monica, CA & Foster City, CA. The position will be responsible for ensuring high quality of data and services across all vendors supporting global R&D portfolio. Other responsibilities include:

Job Responsibility:

  • 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.
  • Understand the 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.
  • Comfortable interacting with internal stakeholders and external vendors.
  • 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 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.

Skills and Requirements:

  • 10+ years of relevant experience in the pharmaceutical or biopharmaceutical industry; and, has a BS or BA with 5 years of relevant experience.
  • PMP certification or equivalent certification
  • Current or former project managers
  • Project management experience in Pharmaceutical or Healthcare industries
  • Excel test required to be submitted
  • Executive presence, excellent communication skills, project management & critical thinking skills

If you are having difficulty in applying or if you have any questions, please contact Kelly Campbell at (+1) 570-277-7115 or k.campbell@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology, and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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