Role: Senior Clinical Data Coordinator - C
Location: Alameda, CA - 94502
Duration: 12 Months
Shift Timings: 8 am to 5 pm

Job Description:

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.

The responsibilities will include: 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.

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.

May perform other duties as required.

Bachelor's degree required (BS degree) 5+ years' experience