What are the responsibilities and job description for the Source Documentation Specialist position at Bioresearch Partner?
We are seeking an experienced and detail-oriented Source Documentation Specialist to join our Clinical Research team. The ideal candidate will play a vital role in creating and ensuring the accuracy and completeness of our source documents. The ideal candidate must have knowledge of RealTime CTMS and eSources.
What you will do in this role:
- All source documents will follow GCP Guidelines and 21 CFR Part 11 Compliance in addition to Care Access Research internal SOP.
- Create templates, worksheets, supplemental source for visits based on detailed review of protocol-defined exams, tests, evaluations, and assessments.
- Review draft source and ensure it is accurate and complete and to ensure that the source document is equipped to record all the required data for the trial.
- Collaborate with the Clinical Research Coordinators when changes need to be made within the source
- Manage daily communication with Site staff and other internal departments
- Maintain version control of all source documents.
Job Type: Full-time
Pay: From $26.00 per hour
Expected hours: 40 per week
Benefits:
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
Schedule:
- 8 hour shift
- Monday to Friday
Work Location: In person
Salary : $26
