Regulatory Affairs Officer Job in Ankleshwar – Icpa Health Products Ltd Hiring (Plant RA) (Regulatory Affairs Officer Job in Ankleshwar) Introduction Are you searching for a Regulatory Affairs Officer job in Ankleshwar, Gujarat? Icpa Health Products Ltd has announced exciting openings for Plant Regulatory Affairs professionals with formulation experience and expertise in global regulatory markets such as the EU, UK, Australia, and Ukraine. This Pharmaceutical Regulatory Affairs job is ideal for B.Pharm and M.Pharm candidates who have 1–4 years of experience in dossier preparation, CTD/ACTD documentation, and ICH guideline compliance. If you are looking to build a strong career in global regulatory submissions and plant-level regulatory compliance, this opportunity can be a valuable step forward. About The Company Icpa Health Products Ltd is a well-established Indian pharmaceutical company founded in 1972. The company is headquartered in Mumbai, Maharashtra, India, and has a stro...
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"MSD Hiring Sr Clinical Trial Coordinator (3–5 Years Exp) – Salary Up to ₹16 LPA | Apply Before 04 March 2026"
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MSD Hiring Sr Clinical Trial Coordinator – Global Clinical Trial Operations (GCTO)
(MSD Hiring Sr Clinical Trial Coordinator)
Introduction
MSD (Merck Sharp & Dohme), globally known as Merck & Co., Inc., USA, has announced an exciting opportunity for experienced Clinical Research professionals. The company is hiring a Sr Clinical Trial Coordinator (CTC) for its Global Clinical Trial Operations (GCTO) team.
This role is ideal for candidates with 3–5 years of hands-on experience in clinical trial documentation, CTMS systems, eTMF management, regulatory submissions, and clinical trial agreements. If you are looking to grow your career in global clinical operations, regulatory compliance, and site start-up management, this is a strong opportunity to work in a multinational pharma environment.
About The Company
MSD, officially known as Merck & Co., Inc., is a leading global biopharmaceutical company headquartered in Rahway, New Jersey, USA. The company was founded in 1891 and has more than 130 years of experience in healthcare innovation.
MSD operates in more than 140 countries worldwide and employs approximately 68,000+ employees globally. The company focuses on discovering, developing, and delivering innovative medicines and vaccines for human and animal health.
MSD is recognized for its strong compliance culture, high ethical standards, and commitment to improving global public health through advanced clinical research and regulatory excellence.
Job Overview Summary
The Sr Clinical Trial Coordinator position is a senior-level operational role within MSD’s Global Clinical Trial Operations (GCTO) department.
This role involves managing clinical trial documentation, supporting regulatory submissions, coordinating site start-up activities, handling budgets and contracts, and ensuring compliance with ICH-GCP guidelines.
The selected candidate will act as a Subject Matter Expert (SME), support junior coordinators, and contribute to process improvements in clinical operations. It is a high-responsibility position in a matrix-driven global environment.
Vacancy Details (Official Information)
Position: Sr Clinical Trial Coordinator Company: MSD (Merck Sharp & Dohme) Department: Global Clinical Trial Operations (GCTO) Experience Required: 3–5 Years Qualification: Bachelor’s Degree (Healthcare / Clinical Research / Administration preferred) Employment Type: Regular Requisition ID: R384567 Job Posting End Date: 04 March 2026 Application Mode: Online
The Sr CTC will ensure smooth coordination of clinical trial sites. This includes tracking essential documents, maintaining safety reports, updating CTMS databases, and ensuring all sites are ready before trial initiation. The role also involves coordinating labeling updates and translation requests.
2. Clinical Trial Documentation & eTMF Management
Proper documentation is critical in clinical research. The candidate will manage the electronic Trial Master File (eTMF), perform reconciliation, execute quality control checks, and prepare Investigator Trial Files (ITF). Maintaining Good Documentation Practices (GDP) compliance is mandatory.
3. Regulatory & Site Start-Up Support
The coordinator will assist in preparing IRB/ERC submission packages and coordinate submissions to regulatory authorities. They will track and study insurance documents and ensure compliance with local regulatory publishing requirements.
4. Budgeting, Contracts & Investigator Payments
This role includes site budget development, Clinical Trial Agreement (CTRA) negotiation, contract lifecycle management, and investigator grant processing. FCPA documentation compliance must be ensured at all stages.
5. Quality Oversight & Leadership
As a senior-level professional, the candidate will mentor junior CTCs, support investigator meetings, and drive continuous improvement initiatives within the GCTO team.
Eligibility Criteria (Official)
Minimum 3–5 years of experience in Clinical Research or Healthcare Bachelor’s Degree (Healthcare / Clinical Research / Administration preferred) Strong knowledge of:
ICH-GCP Guidelines Clinical Trial Compliance CTMS & Clinical IT Systems eTMF Documentation Clinical Trial Agreements (CTA/CTRA) Good Clinical Data Management Practices (GCDMP)
Skills Required (Expanded)
Strong Microsoft Excel and IT system proficiency Hands-on experience in CTMS platforms Knowledge of regulatory submission processes Clinical documentation and data accuracy skills Budget negotiation and contract handling capability Time management and multitasking ability Strong communication and stakeholder coordination skills Ability to work in a global, cross-functional team environment
Salary Estimate (India Equivalent)
For Senior Clinical Trial Coordinator roles in multinational pharma companies and CROs, the estimated salary range in India can be:
₹10,00,000 – ₹16,00,000 per annum (Estimated CTC)
The final compensation may vary depending on experience, country location, and negotiation skills.
Interview Details (Official)
Application Mode: Online through the official MSD careers portal Shortlisting: Based on experience and qualifications Interview Rounds: HR Screening + Technical Round + Final Managerial Discussion The selection process may vary depending on location and business needs
Required Documents (For Application & Interview)
Updated CV with clinical trial experience Educational certificates Experience letters from previous employers CTMS/eTMF system exposure details Proof of regulatory submission experience Salary slips (if required) Government ID proof
Location
MSD operates globally. The exact job location will be mentioned in the official job posting page. Candidates should check the official link for location confirmation.
Apply Method
Interested candidates must apply online through the official MSD career portal:
Q1. What experience is required for a Senior CTC position at MSD? Minimum 3–5 years of experience in Clinical Research or the Healthcare domain.
Q2. Is CTMS knowledge mandatory? Yes, hands-on experience in CTMS and eTMF systems is highly preferred.
Q3. What is the salary range for this position? The estimated salary in India equivalent is ₹10–16 LPA, depending on experience.
Q4. Is this a permanent role? Yes, this is a regular employment position.
Q5. What is the last date to apply? 04 March 2026.
Final Conclusion
MSD’s Sr Clinical Trial Coordinator opportunity is an excellent career move for professionals aiming to grow in global clinical trial management. With responsibilities in regulatory compliance, site start-up operations, documentation control, budgeting, and contract management, this role offers significant exposure in international clinical research operations.
If you have strong expertise in CTMS, eTMF documentation, and clinical trial agreements, this position can accelerate your career in multinational pharma clinical operations.
Candidates are encouraged to apply before the closing date and carefully review all eligibility requirements on the official MSD website.
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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