Syngene Hiring Senior Clinical Research Associate

Syngene Opens CRA Opportunity for Life Science & Pharmacy Professionals

Clinical research hiring in India continues to grow, and Syngene International has announced a new opening for the role of Senior Clinical Research Associate in Bangalore. For professionals with a background in pharmacy and life sciences, this opportunity offers a direct path into advanced clinical trial management and global drug development projects.

As pharmaceutical companies accelerate clinical trials and regulatory submissions, experienced clinical research professionals are in strong demand. Roles like Senior Clinical Research Associate allow candidates to work closely with investigators, study sites, and global research teams driving new therapies toward approval.

Company Overview

Syngene International Ltd is a globally recognized contract research, development, and manufacturing organization (CRDMO). The company provides integrated scientific services that support pharmaceutical, biotechnology, and healthcare companies from early discovery research to commercial manufacturing.

Headquartered in India, Syngene collaborates with leading global pharmaceutical organizations to accelerate innovation in drug discovery and clinical development. The company is widely respected for its strong compliance culture, scientific expertise, and commitment to quality and safety in research operations.

Career Outlook for Clinical Research & Safety Science Professionals in 2026

The clinical research industry is entering a phase of rapid growth as pharmaceutical companies invest heavily in clinical trials, drug safety monitoring, and regulatory compliance. By 2026, experts predict strong demand for professionals skilled in clinical trial monitoring, pharmacovigilance, and safety science analytics.

Clinical Research Associates and Safety Science Analysts will play a critical role in ensuring patient safety, maintaining trial integrity, and supporting regulatory submissions worldwide. Professionals who gain experience in monitoring clinical trial sites, Good Clinical Practice guidelines, and regulatory documentation will have strong long‑term career prospects in global CROs and pharmaceutical companies.

Job Role & Responsibilities

The Senior Clinical Research Associate will be responsible for managing clinical trial sites and ensuring studies are conducted in accordance with Good Clinical Practice guidelines and regulatory standards.

Key responsibilities include:

• Conduct site selection, site initiation, monitoring, and close‑out visits for clinical trials
• Manage assigned study sites, protocols, and therapeutic areas
• Provide protocol and study training to investigators and site staff
• Maintain communication with study sites to monitor ongoing research progress
• Ensure clinical trial data quality and regulatory compliance
• Track regulatory submissions and ethics committee approvals
• Monitor subject recruitment, case report form completion, and data query resolution
• Prepare site monitoring reports and documentation for project management

The role requires strong coordination between investigators, regulatory teams, and clinical project managers to maintain high standards of clinical research and patient safety.

Eligibility / Qualifications

Candidates applying for this clinical research role should meet the following criteria:

• M.Sc, M.Pharm, Pharm.D, BAMS, BDS, MDS, BHMS or any Life Science degree
• Prior experience as a Clinical Research Associate (CRA)
• Strong knowledge of Good Clinical Practice (GCP) and clinical trial processes
• Excellent communication and teamwork skills
• Ability to work in fast‑paced research environments and meet project deadlines

Relevant education backgrounds may include: M.Pharm, Pharm.D, M.Sc Clinical Research, M.Sc Biotechnology, M.Sc Microbiology, M.Sc Biochemistry, B.Pharm, BDS, BAMS, BHMS, MDS.

Location & Salary

Location: Bangalore, India

Salary: Competitive salary package based on experience and clinical research expertise. Leading CRO organizations often offer strong compensation packages along with performance incentives and career advancement opportunities.

Application Process

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

Apply here:
https://careers.syngeneintl.com/job/Senior-Clinical-Research-Associate/1357980966/

Applicants should prepare an updated resume highlighting clinical trial monitoring experience, regulatory knowledge, and therapeutic area expertise.

Frequently Asked Questions

Who can apply for the Syngene Senior CRA role?
Candidates with degrees in Pharmacy, Clinical Research, Medicine, Dentistry, Ayurveda, Homeopathy, or Life Sciences with CRA experience can apply.

What does a Clinical Research Associate do?
A CRA monitors clinical trial sites, ensures compliance with Good Clinical Practice guidelines, manages study documentation, and verifies data quality during clinical research studies.

Is prior experience required for this role?
Yes. Syngene is seeking candidates with experience working as a Clinical Research Associate.

What career growth opportunities exist for CRAs?
Clinical Research Associates can advance to roles such as Senior CRA, Clinical Project Manager, Clinical Trial Manager, or Regulatory Affairs specialist within pharmaceutical and CRO organizations.

Summary

Category	Details
Company	Syngene International Ltd
Vacancies	Senior Clinical Research Associate
Required Education	M.Pharm, Pharm.D, M.Sc Clinical Research, M.Sc Biotechnology, M.Sc Microbiology, M.Sc Biochemistry, B.Pharm, BDS, BAMS, BHMS, MDS
Experience	Prior experience as Clinical Research Associate
Location	Bangalore
Department	Clinical Operations

Tagged as: Pharma Jobs in Bangalore