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Senior Clinical Research Associate

Company

Collabera

Address Alameda, CA, United States
Employment type CONTRACTOR
Salary
Category Medical Equipment Manufacturing,Biotechnology Research,Pharmaceutical Manufacturing
Expires 2023-08-25
Posted at 9 months ago
Job Description

Must Haves:

  • Previous experience within the Medical Device or Pharma industry
  • Comfortable working with a lot of documentation
  • Coordinator and communicate effectively
  • Ability to multitask.
  • Experience working on Clinical Trial Research and Clinical Research Trial Documentation

Key Duties/Responsibilities:

  • Protocol review, CRF design, creation of CRF completion guidelines and data entry guidelines, database design, validation check definition, data review, query generation and resolution, DM Status reports
  • Will be responsible for internal and outsourced data management activities in support of clinical research studies. Will lead 1-3 Clinical Data Management Study sub teams. Will support or lead the data management activities for clinical trials in collaboration with Clinical and Regulatory.
  • SR CDC will ensure timely entry of CRF's by Data coordinators/Data Entry, create DM plans, perform SAE reconciliation, coordinate quality control audits, and review final reports, tables, and listings.

Education/Experience Requirements:

  • 5+ years’ experience in Clinical Research
  • Bachelor’s Degree – Any life sciences related degree

Pay rate:

· $60-70/Hr