Clinical Research Coordinator III
4 weeks ago
Medasource is seeking a highly skilled Clinical Research Coordinator III to join our team. As a key member of our research team, you will be responsible for coordinating all clinical research activities with minimal supervision.
Key Responsibilities:
- Coordinate and oversee all aspects of clinical research projects, including study start-up, site qualifications, initiation, monitoring, and close-out visits.
- Ensure strict adherence to study protocols and regulatory requirements throughout all study activities.
- Manage regulatory compliance and documentation processes, including preparing and maintaining regulatory documents.
- Promote ethical conduct in research and ensure integrity in all aspects of study conduct and data handling.
- Manage logistical and administrative aspects of clinical research projects, including maintaining inventory of supplies and equipment.
- Manage participant engagement throughout clinical research studies, including identifying and recruiting eligible subjects.
- Manage the data lifecycle in clinical research, including abstracting information from medical records and entering data into case report and study forms.
- Provide comprehensive training and mentorship to research personnel.
Requirements:
- Bachelor's degree and two or more years research experience required.
- Strong organizational skills with ability to manage multiple simultaneous studies.
- Strong verbal and written communications skills.
- Strong knowledge of FDA, HSR, and GCP Guidelines.
- Ability to foster an inclusive environment where all team members feel valued and respected.
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