Clinical Research Coordinator

Educational Qualification/s

Bachelor's degree in Lifesciences /medical, Biotech, public health required +

Certification in Clinical Research & basic knowledge of GCP

Experience - 0-2 Years

Job Duties & Responsibilities:

• Coordinates with Principal Investigator, CRO, Sponsor and Fortis central administration to help ensure that clinical research and related activities are performed in accordance with Protocol, DCGI Schedule Y & FDA policies and procedures.
• Assists the PI in the conduct of the study around issues related to protocol requirements, Patient schedule of visits, execution of research plan.
• Essential study related documentation, Site setup, Patient database searching, assist in ICF administration, maintain TMF & patient source files, eCRF filling, SAE reporting etc.
• CRC will use clinical skills and empathy to help study patients with study related procedures
• Building and maintaining relationships with study subjects- Establishing trust with the study patients offering highest level of care & monitoring for study subjects
• Communication/Follow‐up- CRC will regularly call participants between visits to check on their well being (especially if long interval between visits)
• Confirm and remind of upcoming appointments