Role OverviewOur clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess certification such as an MA, phlebotomy, or similar and have a strong desire to work directly with patients.
What You Will Do
Conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc. Performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
Why It Might Be a Fit
A lover of patient interaction and skilled at providing patient care, a team player with a bias for action and an attitude that takes personal responsibility, skilled in all aspects required for conducting an IRB approved clinical trial protocol.
Requirements
- legal authorization to work in the US
- certification such as an MA, phlebotomy, or similar
Benefits
- Competitive compensation
- 401(k) with Company match
- Short- and Long-Term Disability
- Health Savings and Flexible Spending Accounts
- Health, Dental and Vision insurance Plans
- Generous PTO
- Adoption Assistance
- Paid Holidays
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