What are the responsibilities and job description for the Research Coordinator position at OrthoArizona?
About OrthoArizona:
At OrthoArizona, we are bringing the best together. Our organization was created to help serve ALL orthopedic and podiatry needs throughout the Valley! We have a wide range of orthopedic surgeons and mid-level providers including physical and occupational therapists.
Today we are one of Arizona’s largest privately owned and most comprehensive orthopedic practices with more than 75 locally and nationally renowned providers across 30 locations, in addition to 2 ambulatory surgical centers and in house state of the art MRI capabilities. At OrthoArizona we are committed to best-in-class patient care, being a pioneer in research and technology, and most importantly, rewarding and recognizing our employees.
As a Research Coordinator with OrthoArizona, you will get to:
At OrthoArizona, we are bringing the best together. Our organization was created to help serve ALL orthopedic and podiatry needs throughout the Valley! We have a wide range of orthopedic surgeons and mid-level providers including physical and occupational therapists.
Today we are one of Arizona’s largest privately owned and most comprehensive orthopedic practices with more than 75 locally and nationally renowned providers across 30 locations, in addition to 2 ambulatory surgical centers and in house state of the art MRI capabilities. At OrthoArizona we are committed to best-in-class patient care, being a pioneer in research and technology, and most importantly, rewarding and recognizing our employees.
As a Research Coordinator with OrthoArizona, you will get to:
- Collaborate with the supervising physician and research team to develop, implement, and manage clinical research protocols.
- Recruit and screen potential study participants, explaining the purpose and procedures of the study and obtaining informed consent.
- Coordinate and conduct study visits, collect and record accurate data, and ensure compliance with study protocols and regulatory requirements.
- Monitor participant safety and well-being throughout the study, promptly reporting any adverse events or deviations from the protocol.
- Assist in maintaining study records, source documentation, and case report forms in adherence to Good Clinical Practice (GCP) guidelines.
- Liaise with study sponsors, regulatory authorities, and ethics committees as needed to ensure study compliance and approvals.
- Maintain effective communication with all stakeholders, providing regular updates on study progress and any challenges encountered.
- 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.
- Participate in the training and education of study team members, as well as study-related educational sessions for participants.
- Bachelor's degree in a related field (e.g., life sciences, nursing, pharmacy) is preferred. Advanced degrees (e.g., Master's) are highly valued.
- Previous experience as a Clinical Research Coordinator or in a similar research-related role is preferred.
- Familiarity with clinical research processes, regulations (FDA, ICH-GCP), and ethical guidelines is essential.
- Knowledge of electronic data capture systems and proficiency in MS Office applications.
- Excellent communication skills, both written and verbal, with the ability to interact professionally with participants and multidisciplinary teams.
- Strong organizational skills and attention to detail to manage multiple tasks efficiently.
- Ability to work independently and collaboratively within a team-oriented environment.
- A passion for advancing medical research and improving patient outcomes.