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Work as Clinical Research Coordinator at St. John Research Institute - Pharm.D Job


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Clinical courses

Work as Clinical Research Coordinator at St. John's Research Institute

The St. John's Research Institute (SJRI) is a part of the St John's National Academy of Health Sciences, which is run by the CBCI Society for Medical Education. From its inception, St. John's has set before it an ideal of excellence in academic courses as well as service to society as a result of which it has truly become holistic both in its outlook and in its approach to the problems of community health.

Post : Clinical Research Coordinator

Brief Description about the Project
Responsible for multiple studies and specifics as per the protocols submitted to IEC.
• Interaction with Patients, Sponsor / CRO, IEC, Lab staff and other departments in the institution and conduct the study according to ICH GCP Guidelines, SOPs' and study protocol guidelines and act as the main line of communication between patients, Investigators and CROs in study conduct  activities.
• Assist in Feasibility questionnaires, Coordinate in pre-site selection visit, site initiation visit.
• Assist the Principle Investigator and Co investigators in screening of subjects by maintaining and updating the list of potentially eligible patients for the ongoing studies

Salary : Rs 20,000/-pm to be escalated depending on job performance
Preferred Qualifications : Degree with life Science background, trained in Clinical research Diploma in clinical research, or MSC Clinical research or Pharm.D,

Language : English, Kannada, Telugu, Tamil
Experience : 2-3 years

Roles and Responsibilities
• Coordinate in screening, Audio-Video consenting, enrolment, periodic study visits and close out visit.
• Ensure that rights and well being of a research participant is protected throughout the duration of the study.
• Coordinate with finance, legal and regulatory team and assist in the preparation of CTAs specific to the trials.
• Assure all study documentation is maintained by completing the source documents for each
• Patient and maintaining and updating Site Master Files.
• Completing CRFs, e-CRFs on time and resolve data queries.
• EDC, InForm & Medios data capture.
• Ensure and maintain inventory of Study consumables like Investigational product handling, storage, dispensing, accountability, tracking temperature, calibration of equipments, sample centrifugation, courier of documents and lab samples shipment.
• Timely preparation, notification and tracking of the Ethics committee submissions.
• Submission of the study progress, amendments, Protocol Deviations, AE's and SAE's to the ethics committee and sponsor in a timely manner.
• Coordinate with the investigator and the safety monitoring team at the time of SAEs.
• Assist in resolving IEC, DCGI and FDA queries.
• Coordinate and participate in monitoring visits with sponsor/CRO and Facilitating inspections/audits.
• Follow up with patients and document in telephone contact report.
• Conduct study closeout visit and archive the documents.
• Maintain record of closeout studies and resolve the post closeout queries.

Position Starting : 01st February 2023

Interested candidates may send their Resume to :
The Principal Investigator
At las Paed and Neo Atlas /other Hemophilia Studies Project

To Apply : E-mail cover letter and curriculum vitae with 3 references (names and email addresses / phone numbers) by on or before 24th January, 2023 to & cc to

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