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Clinical Research Coordinator Jobs
Company | Medix™ |
Address | Atlanta, GA, United States |
Employment type | FULL_TIME |
Salary | |
Category | Research Services,Hospitals and Health Care,Pharmaceutical Manufacturing |
Expires | 2023-05-10 |
Posted at | 1 year ago |
We are looking for an experienced Clinical Research Coordinator to join our team. This is a great opportunity to join a growing team that is changing the future of therapeutics. Prior Clinical Research Coordinator experience is required, and candidates with at least 3 years of experience working in clinical trials are who we are looking for to join a team that focuses on personal development and a work life balance. This role is responsible for the successful conduct of clinical trials under the oversight of the principal investigator. The CRC will be responsible for both clinical and administrative duties related to the conduct of clinical research at the site.
RESPONSIBILITIES
- Ensuring that the necessary supplies and equipment for a study are in stock and in working order
- Provide responsive and diligent collaboration with sponsor/CRO study teams, including prompt resolution of queries and other action items
- Abide by local, state, GCP, ICH and FDA guidelines and regulations for the conduct of clinical trials
- Complete all required organization and study specific training in timely manner, including attendance at offsite investigator meetings
- Engaging with subjects and understanding their concerns.
- Overseeing the smooth running of clinical trials at site in collaboration with study investigator(s)
- Supervision and training of site research site staff, including study coordinators, research assistants and lab technicians
- Monitoring research participants to ensure adherence to study participation
- Collecting source obtained from research and transcribe into case report forms
- Provide clinical research training and mentoring to study team
- Process study labs per requirements
- Participate in the planning and conduct of research participant recruitment efforts
- Conduct the proper consenting of research participants
- Perform medically qualified clinical procedures such as vital signs, EKG and phlebotomy
REQUIREMENTS
- Currently trained in phlebotomy, performance of vital signs, medical history collection, and administration of EKGs
- Outstanding written and verbal communication
- Exceptional interpersonal and customer service skills
- 3+ years experience as a clinical research coordinator
- Excellent organizational skills
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