JIPMER BPharma Clinical Trial

JIPMER BPharma Clinical Trial Coordinator Job – Applications Invited

JIPMER BPharma Clinical Trial Coordinator Job – Applications Invited. BPharma Job openings at JIPMER. Interested and eligible applicants can check out all of the details on the same below:


Applications are invited by the HOD, Department of Nephrology, Jawaharlal Institute of Postgraduate Medical Education and Research (JIPMER), Puducherry from candidates for the following post for “A prospective, interventional, multicentre, Phase IV, open-label, single arm study to assess the safety and effectiveness of finerenone in participants from india with chronic kidney disease associated with type 2 diabetes”, study. 

Job Title: Clinical Trial Coordinator

Location:  Puducherry

Age: Should be less than 35 years as on 31-08-2023

Mode of Recruitment: Walk in Interview with written test.

Terms and conditions

  1. Tenure for post is Twelve Months, which may be extended for the full project duration. This position will be purely on a temporary/contractual basis for the specified period of time and based on project.
  2. Applicants with research experience, good communication skills in Tamil and basic computer skills will be preferred. 
  3. The remuneration is consolidated; Benefit of provident fund, HRA, CCA, Leave Travel Concession, Medical Claim etc. are not applicable.
  4. The appointment can be terminated at any time with one month’s notice without assigning any reason or if the person’s work is considered unsatisfactory by the competent authority. 
  5. If the appointee wishes to resign his/her job, he/she has to serve one month’s notice or remit one month’s salary or pay thereof, as the case may be proportionate to the shortfall in the notice period 
  6. The appointee shall be on a full time appointment for this project and shall not accept any other assignment nor engage himself/herself, paid or otherwise during the period of appointment.
  7. No TA/DA will be admissible to appear in the interview. 
  8. Only candidates who can join by 01-10-2023 need to apply, as the positions are to be filled on an urgent basis.
  9. Since the posts are purely temporary, the incumbents selected will have no claim for regular appointments in JIPMER or continuation of his/her services in any other project. 
  10. Canvassing in any form will lead to disqualification. 
  11. Interested candidates are requested to report to the Department of Nephrology at 9.00AM on 21-09-2023 with Documents/ Certificates for Verification.
  12. If More candidates appear for a walk -in interview, candidates will be shortlisted by written test. 
  13. Shortlisted candidates shall be called for an interview scheduled on 21-09-2023 at 2.00PM @ Department of Nephrology. 

Documents to be Brought on Walk in Interview

  1. Proof for date of birth 
  2. Proof of residence 
  3. Qualification and experience certificates 
  4. CV

Dr Sreejith Parameswaran
Professor & Head
Department of Nephrology
JIPMER, Puducherry-06

Qualification:  A three-year bachelor’s degree in Paramedical sciences/Life Sciences/B.Pharm 

Experience:Clinical trial experience of 6 or more months  Computer Skills with data entry of patient level database

Remuneration: INR 15,000 (Consolidated)

Click here for the notification

 Possible Interview Questions and Answers:

  1. Can you explain your understanding of the study’s objective and design?

Answer:The study aims to assess the safety and effectiveness of finerenone in individuals from India who have chronic kidney disease associated with type 2 diabetes. It’s a Phase IV, multicentre, open-label, single-arm study, which means it involves a large-scale evaluation of the drug’s real-world use in a diverse patient population.

  1. What qualifications and experience do you have that make you suitable for this role?

Answer:I hold a [mention your relevant degree, e.g., Bachelor’s in Life Sciences or Nursing], and I have [mention your years of experience, e.g., 3 years] of experience working in clinical trial coordination. My experience includes managing various aspects of clinical trials, including patient recruitment, data collection, and regulatory compliance.

  1. How would you ensure the ethical conduct of this clinical trial?

Answer: Ethical conduct in clinical trials is of utmost importance. I would ensure ethical standards are maintained by following the study protocol, obtaining informed consent from participants, and regularly reviewing and reporting any adverse events or deviations from the protocol to the Institutional Review Board (IRB).

  1. Can you describe your experience with patient recruitment for clinical trials?

Answer:In my previous role, I was responsible for patient recruitment for multiple clinical trials. I utilized various strategies such as collaborating with healthcare providers, conducting community outreach programs, and utilizing digital platforms to reach potential participants. I also ensured that all recruited participants met the study’s inclusion criteria.

  1. How would you handle adverse events or unexpected issues during the trial?

Answer:When handling adverse events or unexpected issues, I would follow the established protocol and immediately report them to the appropriate regulatory authorities, such as the IRB and the study sponsor. It’s crucial to document all relevant details, communicate with the study team, and take necessary actions to ensure participant safety and data integrity.

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