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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 |
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
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