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Company | OrthoArizona |
Address | Gilbert, AZ, United States |
Employment type | PART_TIME |
Salary | |
Category | Hospitals and Health Care |
Expires | 2023-09-03 |
Posted at | 8 months ago |
Position: Clinical Research Coordinator
- Collaborate with the supervising physician and research team to develop, implement, and manage clinical research protocols.
- Participate in the training and education of study team members, as well as study-related educational sessions for participants.
- Recruit and screen potential study participants, explaining the purpose and procedures of the study and obtaining informed consent.
- Liaise with study sponsors, regulatory authorities, and ethics committees as needed to ensure study compliance and approvals.
- Monitor participant safety and well-being throughout the study, promptly reporting any adverse events or deviations from the protocol.
- Maintain effective communication with all stakeholders, providing regular updates on study progress and any challenges encountered.
- Coordinate and conduct study visits, collect and record accurate data, and ensure compliance with study protocols and regulatory requirements.
- Assist in maintaining study records, source documentation, and case report forms in adherence to Good Clinical Practice (GCP) guidelines.
- Contribute to the preparation and submission of research manuscripts, abstracts, and presentations for scientific conferences.
- Ensure proper storage and accountability of investigational products and study supplies.
- Knowledge of electronic data capture systems and proficiency in MS Office applications.
- Ability to work independently and collaboratively within a team-oriented environment.
- Familiarity with clinical research processes, regulations (FDA, ICH-GCP), and ethical guidelines is essential.
- Excellent communication skills, both written and verbal, with the ability to interact professionally with participants and multidisciplinary teams.
- Bachelor's degree in a related field (e.g., life sciences, nursing, pharmacy) is preferred. Advanced degrees (e.g., Master's) are highly valued.
- Strong organizational skills and attention to detail to manage multiple tasks efficiently.
- Previous experience as a Clinical Research Coordinator or in a similar research-related role is preferred.
- A passion for advancing medical research and improving patient outcomes.
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