TMC Muzaffarpur Recruitment 2026: Trial Coordinator Walk-in Interview

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TMC Muzaffarpur Recruitment 2026: Trial Coordinator Walk-in Interview ( TMC Muzaffarpur Recruitment 2026 ) Tata Memorial Centre (TMC) has announced a project-based recruitment opportunity for the post of Trial Coordinator at Homi Bhabha Cancer Hospital and Research Centre (HBCH&RC), Muzaffarpur, Bihar . This recruitment is associated with a breast cancer screening research project and offers an opportunity for eligible Science graduates and postgraduates who hold a mandatory Postgraduate Diploma in Clinical Research. According to the recruitment details provided, one vacancy is available, with a consolidated monthly remuneration of ₹30,000. Eligible candidates can attend the walk-in interview scheduled for 29 October 2026 . Outstation candidates who wish to request an online interview must submit their application documents by 26 October 2026, before 3:00 PM . Candidates interested in Clinical Research Jobs, Clinical Trial Jobs, Hospital Research Jobs, and Life Science Jobs shou...

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"ProPharma Hiring Pharmacovigilance Safety Scientist in India – Apply Now"

"ProPharma Hiring Pharmacovigilance Safety Scientist in India – Apply Now"



(ProPharma Hiring Pharmacovigilance)



Are you passionate about drug safety and pharmacovigilance? ProPharma, a trusted global leader in regulatory sciences, clinical research, and drug safety, is inviting applications for the Pharmacovigilance Safety Scientist role in India. This position offers an excellent opportunity to work on global projects and contribute to improving patient safety worldwide.


Key Responsibilities:-

As a Pharmacovigilance Safety Scientist at ProPharma, you will be responsible for:

  • Authoring aggregate safety reports such as PSURs, PBRERs, PADERs, Annual Reports, ACO, and DSUR.
  • Developing and maintaining Risk Management Plans (RMPs).
  • Preparing Signal Management Reports and conducting literature searches.
  • Reconciling process trackers and validating extracted data.
  • Generating and reviewing line listings from safety databases.
  • Supporting ad-hoc pharmacovigilance activities as per project requirements.
  • Ensuring all deliverables meet ICH-GCP, FDA, EMA, and global PV regulations.
  • Contributing to SOPs, deviations, and CAPA activities.
  • Analyzing large volumes of safety data with precision and accuracy.


Required Qualifications & Skills:-

  • Education: Bachelor’s/Master’s in Pharmacy, Nursing, Life Sciences, or related health sciences.
  • Experience: Minimum 2+ years in pharmacovigilance, with expertise in medical writing, signal detection, or literature review.
  • Strong understanding of global PV regulations.
  • Excellent communication, writing, and analytical skills.
  • Proficiency in MS Office tools and PV database applications.
  • Ability to work in a matrix and multicultural environment.


Why Join ProPharma?

  • Be part of a global leader in pharmacovigilance and regulatory sciences.
  • Contribute to patient safety and global healthcare improvement.
  • Opportunity to work with a collaborative, diverse, and inclusive team.
  • Strong career growth in drug safety, PV, and medical writing.


How to Apply:-

Interested candidates can apply directly through the official link below:

👉 Apply Here – Pharmacovigilance Safety Scientist at ProPharma India


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