Syngene Hiring Senior Clinical Research Associate

Senior CRA Openings | Syngene Bangalore Clinical Research

Apply for Senior Clinical Research Associate role at Syngene, Bangalore. Qualification: M.Sc/M.Pharm/Pharm.D/Life Sciences, 3–9 years’ experience.

Syngene International Ltd., a leading global contract research, development, and manufacturing organization (CRDMO), is inviting applications for the role of Senior Clinical Research Associate (CRA) in its Clinical Operations Department at Bangalore, India. This opportunity is ideal for experienced clinical research professionals looking to advance their careers in clinical trials, site management, and regulatory compliance with one of the most respected names in the life sciences industry.

Company Overview

Syngene International (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022) is an innovation-driven research organization that provides integrated scientific solutions from early drug discovery to commercial supply. With a workforce of over 4,500 scientists and state-of-the-art facilities spanning 1.9 million sq. ft., Syngene partners with global leaders including Amgen, Baxter, Bristol-Myers Squibb, Herbalife, GSK, and Merck KGaA. The company emphasizes safety, quality, integrity, and professionalism, making it a trusted partner in pharmaceutical and biotechnology research worldwide.

Job Role & Responsibilities

As a Senior CRA at Syngene, you will be responsible for:

• Conducting site selection, initiation, monitoring, and close-out visits in line with SOPs, GCP guidelines, and regulatory requirements.
• Managing assigned sites, protocols, and therapeutic areas while ensuring data quality and study integrity.
• Delivering protocol and study-related training to assigned sites.
• Establishing regular communication with clinical sites to manage project expectations.
• Investigating quality issues and collaborating with Project Managers for CAPA (Corrective and Preventive Action) implementation.
• Tracking submissions and approvals from regulatory and ethics committees.
• Overseeing patient recruitment, CRF (Case Report Form) completion, and data query resolution.
• Preparing documentation such as visit reports, follow-up letters, and study action plans.
• Supporting Clinical Project Managers in study design, documentation, and project-level coordination.
• Leading projects as Lead CRA, if assigned, including delegating tasks and coordinating with project teams.

Eligibility / Qualifications

• Educational Qualification: M.Sc, M.Pharm, Pharm.D, BAMS, BDS, MDS, BHMS, or any Life Science degree.
• Experience: 3–9 years of relevant experience in clinical research, clinical trial monitoring, and site management.
• Skills Required:
  • Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
  • Excellent communication and organizational skills.
  • Ability to work under pressure, multitask, and prioritize effectively.
  • Strong teamwork and problem-solving abilities.

Location & Salary

• Location: Bangalore, Karnataka, India
• Salary: Competitive package based on experience and industry standards.

Application Process

Candidates who meet the above criteria are encouraged to apply directly via Syngene’s career portal:

Apply Here

Apply before 23rd August 2025 to secure your opportunity!

Why Join Syngene?

• Be part of a world-class CRDMO with global collaborations and partnerships.
• Contribute to innovative clinical research supporting new drug development.
• Career growth with structured training and development opportunities.
• Work in a collaborative culture that values safety, excellence, and integrity.
• Equal opportunity employer fostering diversity and inclusion.

Frequently Asked Questions (FAQs)

Q1: What qualifications are required for this CRA role?
Applicants should have M.Sc, M.Pharm, Pharm.D, or a Life Sciences degree (including BAMS, BDS, MDS, BHMS).

Q2: How much experience is needed?
Candidates should have 3–9 years of experience in clinical research, clinical trial monitoring, or site management.

Q3: What will my core responsibilities be?
You will handle site visits, monitoring, regulatory compliance, patient recruitment oversight, and study documentation.

Q4: Is prior CRA experience mandatory?
Yes, relevant prior experience in clinical research and monitoring is required.

Q5: Where is this job located?
The role is based at Syngene’s Bangalore facility, Karnataka.

Q6: How can I apply?
Interested applicants can apply via the official Syngene careers page using the application link provided.

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