Syngene Hiring Pharmacist for Clinical Trial Supply Management in Bangalore

Syngene Hiring Clinical Trial Pharmacist in Bangalore for M.Pharm

Global contract research and development organization Syngene International has announced hiring for the position of Pharmacist within its Biometrics division in Bangalore. The role focuses on clinical trial supply management and investigational product handling, making it a valuable opportunity for pharmacy professionals interested in clinical research operations.

As pharmaceutical companies continue expanding global clinical trials, the demand for pharmacists who understand investigational product (IP) management and regulatory compliance is growing rapidly. This position allows professionals to work closely with clinical trial teams and contribute to drug development programs that ultimately lead to new therapies reaching patients.

For pharmacy graduates looking to move beyond traditional retail or hospital pharmacy roles, clinical trial pharmacy operations offer a highly specialized career path in the pharmaceutical research industry.

Company Overview

Syngene International Ltd. is a globally recognized contract research, development, and manufacturing organization (CRDMO). Established in 1993, the company provides integrated scientific services to pharmaceutical, biotechnology, nutrition, animal health, and consumer goods companies worldwide.

The organization collaborates with several leading global pharmaceutical companies including Bristol‑Myers Squibb, Baxter, Amgen, GlaxoSmithKline, Merck KGaA, and Herbalife. Through its advanced research facilities and scientific expertise, Syngene supports clients in accelerating drug discovery, development, and commercialization.

With thousands of scientists and research professionals working across multiple disciplines, the company plays a crucial role in improving research productivity and reducing the time required for pharmaceutical innovation.

Career Outlook for Clinical Supply & Safety Science Professionals in 2026

Clinical trial supply management is becoming an increasingly critical function within pharmaceutical research organizations. By 2026, pharmaceutical companies and contract research organizations are expected to invest heavily in clinical trial logistics, investigational product management, and regulatory‑compliant drug supply chains.

Pharmacists involved in clinical trial supply operations ensure that investigational medicinal products are handled, labeled, stored, and distributed according to strict regulatory standards. Their work directly supports clinical trials conducted across hospitals and research sites globally.

Professionals who begin careers in clinical supply management can later progress into roles such as Clinical Trial Supply Manager, Clinical Operations Manager, Clinical Research Associate, or Regulatory Affairs Specialist. With increasing complexity in global clinical trials, expertise in investigational product management and regulatory compliance remains highly valuable.

Job Role & Responsibilities

The Pharmacist will play a central role in managing investigational medicinal products used in clinical trials conducted by Syngene.

Key responsibilities include:

• Prepare protocol‑specific pharmacy plans and secondary labeling plans for clinical trials
• Manage receipt, verification, and storage of Investigational Medicinal Products (IMP) and Non‑Clinical Supplies (NCS)
• Perform labeling and relabeling activities including expiry extension and secondary labeling
• Coordinate supply and resupply of investigational products to clinical trial sites
• Ensure shipments maintain required temperature conditions during transportation
• Prepare shipment documentation and manage inventory of clinical trial supplies
• Maintain adequate supply of investigational products at research sites
• Conduct reconciliation and return processes for investigational products after study completion
• Witness destruction of unused investigational products according to approved procedures
• Maintain documentation for all clinical supply activities in compliance with regulatory guidelines

These responsibilities ensure that clinical trials receive the correct drug supplies while maintaining strict quality and compliance standards.

Compliance & Documentation Responsibilities

The role requires strict adherence to international clinical research regulations and documentation practices.

Responsibilities include:

• Ensure compliance with ICH‑GCP guidelines and local regulatory requirements
• Maintain standard operating procedures and clinical supply documentation
• Support internal and external audits related to clinical trial supply management
• Ensure calibration and maintenance of clinical supply unit instruments

Accurate documentation and regulatory compliance are essential for maintaining data integrity and patient safety in clinical research studies.

Eligibility / Qualifications

Candidates interested in this clinical research pharmacist role should meet the following criteria:

• Master’s degree in Life Sciences or Pharmacology
• Strong knowledge of clinical trial supply management and investigational product handling
• Understanding of ICH‑GCP guidelines and Indian regulatory requirements
• Familiarity with Microsoft Office tools including Word, Excel, and PowerPoint
• Experience supporting audits and documentation processes

Relevant education backgrounds may include: M.Pharm Pharmacology, M.Pharm Pharmaceutics, M.Pharm Pharmaceutical Analysis, M.Sc Life Sciences, M.Sc Pharmacology.

Location & Salary

Location: Bangalore, Karnataka, India

Application Process

Interested candidates can apply through the official Syngene careers portal using the link below.

Apply here:
https://careers.syngeneintl.com/job/Bangalore-Pharmacist-KA-560100/1332430166/

Applicants should submit an updated resume highlighting experience in clinical trial pharmacy operations, regulatory compliance knowledge, and investigational product management.

Early applications are recommended as clinical research roles in leading CRO organizations often receive strong interest from qualified candidates.

Frequently Asked Questions

Who can apply for the Syngene Pharmacist role?
Candidates with a Master’s degree in Life Sciences or Pharmacology with knowledge of clinical trial operations can apply.

What does a clinical trial pharmacist do?
A clinical trial pharmacist manages investigational drug supplies, labeling, storage, and distribution to clinical research sites while ensuring compliance with regulatory guidelines.

Is knowledge of ICH‑GCP required for this role?
Yes. Understanding ICH‑GCP and regulatory requirements is important for professionals involved in clinical trial supply management.

What career growth opportunities exist in clinical trial pharmacy roles?
Professionals may progress into Clinical Supply Manager, Clinical Operations Specialist, Regulatory Affairs professional, or Clinical Research Associate roles.

Summary

Category	Details
Company	Syngene International Ltd
Vacancies	Pharmacist – Clinical Trial Supply Management
Required Education	M.Pharm Pharmacology, M.Pharm Pharmaceutics, M.Pharm Pharmaceutical Analysis, M.Sc Life Sciences
Experience	Experience in clinical trial supply or IP management preferred
Location	Bangalore, Karnataka
Department	Biometrics / Clinical Supply Management

Tagged as: Pharma Jobs in Bangalore