Clinical Research Coordinator Job at SJRI | Apply by May 27
St. John’s Research Institute (SJRI) is inviting applications for the role of Clinical Research Coordinator for the Multiple Myeloma Project. This is an excellent opportunity for life sciences graduates or Pharm D professionals, especially those with training in clinical research, to work in a highly reputed institution and gain hands-on experience in clinical trial coordination. The role begins on June 1, 2025, and offers structured exposure to ICH-GCP, ethics, regulatory submissions, and patient interactions.
Clinical Research Co-ordinator – Multiple Myeloma Project
Division Non Division User
Project / Title Multiple Myeloma Project
Contact Person HR
Contact No 080497011/7021
Job Details
Brief Description about the Project
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 Principal Investigator and Co investigators in screening of subjects by maintaining and updating the list of potentially eligible patients for the ongoing studies
Clinical Research Co-ordinator
Position Starting:
1st June 2025No. of Vacancy: one
Salary: 20,000/ month to be escalated depending on job performance
Language: English, Kannada and Hindi, Telugu
Experience: 0 -1 year
Preferred Qualifications: Degree with life Science background, trained in Clinical research e.g. Diploma in clinical research, or MSC Clinical research and Pharm D
Minimum Experience: No. required: fresher
Maximum Experience: No. required: 1 year
Last Day for Receiving Application: 27.05.2025
Roles 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 & Medidata data capture.
- Ensure and maintain inventory of Study consumables like Investigational product handling, storage, dispensing, accountability, tracking temperature, calibration of equipment’s, 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 SAEs 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. GC-P/C-IRMS, Orbitrap-MS) and IR spectroscopy (FTIR) for the ongoing research project.
Interested candidates may send their Resume to:
The Principal Investigator
Multiple Myeloma Project
SJRI
To Apply: E-mail cover letter and curriculum vitae with 3 references (names and email addresses / phone numbers) by on or before 27th May 2025 hemtrials.stjohns@sjri.res.in & cc to hr@sjri.res.in
For more information, please visit our website www.sjri.res.in
Can Contact us on the following Numbers 080-49467010 / 49467011
Keywords: Clinical Research Coordinator, Multiple Myeloma Project, Clinical Research, St. John’s Research Institute, Clinical Research Coordinator Job
