Macleods Hiring Clinical Trials – Deputy General Manager

Clinical Research Job Opening for Science Postgraduates – Macleods Hiring in Mumbai

Opportunity for Postgraduates in Clinical Research or Life Sciences with 5–10 years of experience to apply for a senior role in Mumbai at Macleods.

Explore a High-Level Opportunity in Clinical Trials at Macleods, Mumbai

Are you a seasoned clinical research professional seeking to work with one of India’s top pharmaceutical companies? Macleods Pharmaceuticals is inviting applications for the role of Deputy General Manager – Clinical Trials at their Mumbai office. This role offers the chance to work on critical clinical trial documentation and protocol development—ideal for experienced candidates passionate about quality and regulatory standards.

Why Consider Macleods for Your Clinical Research Career?

Macleods has established itself as a trusted name in the pharmaceutical industry with a focus on innovation, patient care, and global regulatory compliance. The Clinical Trials team plays a vital role in ensuring product safety and efficacy through scientific, structured, and ethical trial documentation. This is your chance to contribute directly to public health and regulatory excellence.

Key Responsibilities in This Role

Drafting & Reviewing Critical Trial Documents

• Prepare and review clinical trial protocols, clinical study reports, informed consent forms, investigator brochures, and patient-facing documents.
• Collaborate with internal stakeholders to ensure accurate scientific input into trial documentation.

Quality Oversight & Compliance

• Perform thorough quality checks of all clinical trial documents.
• Ensure that documentation aligns with global GCP (Good Clinical Practice) and ICH guidelines.

Cross-functional Collaboration

• Work alongside medical writers, regulatory experts, and clinical operations teams.
• Serve as the central contact for all documentation needs within the trial lifecycle.

Eligibility Criteria & Candidate Profile

Required Educational Background

• Postgraduate Degree in Life Sciences, Clinical Research, Pharmacy, Biotechnology, or related fields.

Experience

• 5 to 10 years of relevant industry experience in medical writing or clinical trial documentation.

Additional Competencies

• Strong command of medical terminology, regulatory writing standards, and data interpretation.
• Ability to manage multiple projects under tight deadlines.

Job Location

Mumbai, Maharashtra – A pharmaceutical hub with numerous career advancement opportunities.

How to Apply

Interested candidates can send their resumes to:

mayuri.muneshwar@macleodspharma.com

For more details, visit the official careers page:

https://www.macleodspharma.com

Related Career Paths Based on Educational Background

Relevant Courses:
Clinical Research, Pharmacy (MPharm), Biomedical Science, Biotechnology, Microbiology, Pharmacology, Regulatory Affairs, Public Health, Biostatistics, and Health Sciences.

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