Trial Coordinator Jobs For BPharm & MPharm Candidates at TMC, Mumbai
Trial Coordinator Jobs For BPharm & MPharm Candidates at TMC, Mumbai. BPharm and MPharm Clinical Trial Coordinator job openings. Interested and eligible applicants can check out all of the details on the same below
Possible Interview Questions for the roles of Trial Coordinators at TMC are posted below
TATA MEMORIAL HOSPITAL
(TATA MEMORIAL CENTRE)
H.R.D. DEPARTMENT
(Grant-In-Aid Institute of Department of Atomic Energy, Government of India)
Ref. No. TMC/AD/ 72 /2023
WALK IN INTERVIEW
ON 20.06.2023
Between 09.30 a.m. & 10.30 a.m
Required Trial Co-ordinator on “A phase II study to evaluate oral chlorophyllin in hemorrgagic cystitis secondary to radiation therapy for pelvic malignancies” (CLARITY Trial) Project (A/c No.4780) Initially for a period of six months.
Post I
Name of the Post: Trial Co-ordinator (Jr)
Qualification: Graduation in Science (e.g. B. Pharm, Life Science, Biotech, Zoology, Botany etc.) with PG Diploma in Clinical Research is mandatory.
Remuneration: Starting Rs.22000/- p.m. depending upon qualification and experience.
Post II
Name of the Post: Trial Co-ordinator (Sr)
Qualification: Post Graduation in Science (e.g. M. Pharm, Life Science, Biotech, Zoology, Botany etc.) with PG Diploma in Clinical Research is mandatory.
Experience: 1 year
of experience in clinical research will be preferred. (Preference will be given to the candidate with TMH experience. Candidates currently working in TMC must bring NOC from their respective HOD at the time of interview.)Remuneration: Starting Rs.23000/- p.m. depending upon qualification and experience.
How to Apply –
Interested candidates may come at Tata Memorial Hospital, 4TH Flr, Dinning Hall, Golden Jubilee Bldg., Dr. E. Borges Marg, Parel, Mumbai – 400012 along with Bio-data, recent passport size photograph, copy of PANCARD, AADHAR Card, original certificates and set of attested copies of all certificates.
For further enquiry please contact No.24177000 Extn. 4666
Possible Interview Questions for the roles of Trial Coordinator at TMC:
- Question: What is the role of a Trial Coordinator in a clinical research project? Answer: The Trial Coordinator plays a crucial role in managing and coordinating various aspects of a clinical research study. They are responsible for overseeing participant recruitment, data collection, regulatory compliance, and ensuring the smooth execution of the study protocol.
- Question: What qualifications and experience do you possess that make you suitable for the position of Trial Coordinator (Jr/Sr)? Answer: For the position of Trial Coordinator (Jr), a graduation degree in Science along with a PG Diploma in Clinical Research is mandatory. In the case of Trial Coordinator (Sr), a post-graduation degree in Science along with a PG Diploma in Clinical Research is required. Relevant experience in clinical research is also preferred for the senior position.
- Question: Can you explain the significance of the CLARITY Trial and its objective? Answer: The CLARITY Trial focuses on evaluating the efficacy of oral chlorophyllin in the treatment of hemorraghic cystitis secondary to radiation therapy for pelvic malignancies. The objective is to assess the potential benefits of chlorophyllin in reducing the severity and incidence of hemorraghic cystitis and improving the quality of life for the patients undergoing radiation therapy.
- Question: How do you ensure regulatory compliance in clinical research studies? Answer: Regulatory compliance is essential to maintain ethical standards and protect the rights and well-being of study participants. As a Trial Coordinator, I would ensure compliance by following established protocols, obtaining informed consent from participants, adhering to Good Clinical Practice (GCP) guidelines, maintaining accurate and complete documentation, and coordinating with regulatory authorities for necessary approvals.
- Question: Describe your experience in coordinating clinical research studies and managing data collection. Answer: If the candidate has relevant experience: I have been involved in coordinating clinical research studies, where I was responsible for participant recruitment, scheduling visits, collecting and recording data, ensuring data quality and integrity, and liaising with the study team and investigators. I have experience in using electronic data capture systems and maintaining strict confidentiality and data security measures.If the candidate is a fresher: Although I do not have direct experience in coordinating clinical research studies, my educational background in [relevant field] and my PG Diploma in Clinical Research have equipped me with the necessary knowledge and skills to perform the role effectively. I am eager to apply my theoretical understanding and learn from experienced professionals in this role.
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