Full Job Description
Successful applicant will be involved in Clinical Trials as a member of site staff.
Responsibilities include:
Patient evaluation through direct patient contact, history, review of medication list and allergies, Physical examination. Review of medical records, determination of Inclusion and exclusionary criteria. Knowledge of GCP is preferred. Successful candidate will be trained in clinical trial management and conduct. Works closely with physician Principal Investigators across multiple therapeutic areas.
Details of role with Paradigm:
The Sub-Investigator is a critical member of the study team as a mid-level practitioner responsible for providing medical guidance and management. The Sub-Investigator provides direct leadership, training, and oversight to site staff including study coordinators and research assistants. The Sub-Investigator overseas the care of study subjects under the guidance of the Principle Investigator.
The Sub-Investigator takes an active role in the Company’s growth objectives. The Sub-Investigator supports the development of new client relationships and the strengthening of existing account relationships with a view to expanding the Company’s portfolio of investigators, studies, clients and therapeutic area experience and expertise. The Sub-Investigator also assists in building and managing positive relationships in the clinical research community to increase the Company’s visibility, reputation, and stature consistent with being a recognized employer and partner of choice.
Job Type: Full-time
Pay: $100,000.00 – $150,000.00 per year
Benefits:
- 401(k)
- 401(k) matching
- Dental insurance
- Flexible schedule
- Flexible spending account
- Health insurance
- Health savings account
- Life insurance
- Paid time off
- Professional development assistance
- Retirement plan
- Vision insurance
Application Question(s):
- Do you have experience in clinical research?
Experience:
- clinical practice: 1 year (Required)
Work Location: In person