Clinical Research Coordinator

Job Description

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/Followup- 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