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Clinical Data Coordinator Jobs
Company | Intellectt Inc |
Address | Alameda, CA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Staffing and Recruiting |
Expires | 2023-08-24 |
Posted at | 9 months ago |
Role: Senior Clinical Data Coordinator - C
Location: Alameda, CA - 94502
Duration: 12 Months on W2 (Possibility of project extension)
Skills Looking For:
- Senior Clinical data coordinators.
- Experience with clinical research trials in med devices.
- Open to pharma as well but would prefer med devices.
- Exp with Clinical research trial documentation and clinical data management.
- Experience using any kind of online eTMF(Electronic Trial Master File).
- Working knowledge of Microsoft office tools - Excel, word, outlook.
- Knowledge knowledge on using statistics.
- SAS experience is nice to have (running the program).
- Must know how clinical trials are run, and know how to draft documents.
- Work with the data management team and interact a lot with the statistics team and clinical team. A lot of cross-functional coordination is needed in terms of documentation. This person will work on more than one study at a time so they must be able to juggle between two or three studies.
- Day to Day Activities: Run reports on a weekly basis. Depending on study; depending on various studies and the phases they are in work will differ. For example, if the study is in the statistical phase they need to draft CRF completion guidelines and the database specifications. Work with the systems team who will design the database by giving them requirements. Some studies are in the maintenance phase, then they will need to look at clinical data, query data review, etc. This person will deal with a lot of documentation work and will read a lot of clinical protocols..
Education and Experience:
- Bachelor required (any scientific degree) with 5+ years exp in clinical research trials.
- Open to Masters degree (Lifesciences, Bio-chemistry, genetics; any research related) but again 5+ years experience is needed as it is a very senior role.
Top Skills:
- Exp working on clinical trial research
- Coordinate and communicate effectively
- Worked with a lot of documentation. Need to be able to juggle between different studies.
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