Care Access is looking to revolutionize access to clinical trials for the benefit of patients everywhere by integrating individuals into their research process and learning the skills necessary to be a Clinical Research Coordinator.
Requirements
- A working knowledge of medical and research terminology
- A working knowledge of federal regulations, Good Clinical Practices (GCP)
- Phlebotomy experience and proficiency required.
- Proficiency in Microsoft Office Suite
Responsibilities
- Record data legibly and enter in real time on paper or e-source documents.
- Collect, process and ship specimens as directed by protocol, under the direction of the CRC.
- Assist with query resolution.
- Update all applicable internal trackers and online recruitment systems.
- Assist with maintaining all site logs.
- Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.
- Obtain informed consent per Care Access Research SOP, under the direction of the Clinical Research Coordinator (CRC).
Other
- This position is for a full-time temporary, hourly role. The duration is 12-months from the decision to hire.
- Candidates must be willing to travel 75% of the time nationwide.
- Ability and willingness to work independently with minimal supervision.
- Ability to learn to work in a fast-paced environment.
- Excellent communication skills and a high degree of professionalism with all types of people
