ManpowerGroup - Alameda, CA

posted 24 days ago

Full-time - Mid Level
Onsite - Alameda, CA
Administrative and Support Services

About the position

The Senior Clinical Data Coordinator will oversee internal and outsourced data management activities for clinical research studies. This role involves leading Clinical Data Management Study subteams and collaborating with Clinical and Regulatory teams to ensure effective data management throughout clinical trials.

Responsibilities

  • Responsible for internal and outsourced data management activities in support of clinical research studies.
  • Lead 1-3 Clinical Data Management Study subteams.
  • Support or lead data management activities for clinical trials in collaboration with Clinical and Regulatory teams.
  • Conduct protocol review, CRF design, and create CRF completion guidelines and data entry guidelines.
  • Design databases, define validation checks, and perform data review.
  • Generate and resolve queries, and prepare DM Status reports.
  • Ensure timely entry of CRFs by Data Coordinators/Data Entry personnel.
  • Create DM plans, perform SAE reconciliation, and coordinate quality control audits.
  • Review final reports, tables, and listings.

Requirements

  • Bachelor's degree in physical, mathematical, or computer science or related field or equivalent.
  • Master's degree preferred.
  • 5+ years of experience in clinical data management.
  • Willingness to perform routine and tedious tasks such as laptop installations and managing user accounts.

Nice-to-haves

  • Interest in project management.
  • Exposure to EDC, eTMF, SharePoint, Business Analytics, and Cloud systems.

Benefits

  • Equal employment opportunities in a professional work environment.
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