Job Description
Role Description
This is a contract role for a Clinical Research Coordinator, located on-site in Bryn Mawr, Pennsylvania. The Clinical Research Coordinator will be responsible for managing the day-to-day clinical trial activities, obtaining informed consent from study participants, ensuring protocol adherence, conducting clinical research tasks, and managing clinical trial documentation.
Qualifications
- Experience in obtaining Informed Consent and ensuring Protocol adherence
- Strong background in Research, with a focus on Clinical Research Experience
- Proficiency in managing Clinical Trials and related tasks
- Excellent organizational and documentation skills
- Ability to work collaboratively in an on-site environment
- Knowledge of regulatory requirements and GCP (Good Clinical Practice) guidelines
- Bachelor’s degree in a related field or equivalent experience
NOTE: This role will start at 20 hrs/week with ability to convert to full-time.
Job Tags
Full time, Contract work,