Syngene Hiring CRA – Clinical Operations

Syngene Hiring CRA – Clinical Operations in Bangalore

Syngene has announced a new hiring opportunity for the position of CRA under the Clinical Operations department at its Bangalore location. The company is inviting applications from experienced clinical research professionals with expertise in clinical trial monitoring, site management, GCP compliance, and clinical operations.

This recruitment drive is attracting candidates searching for CRA jobs in Bangalore, clinical research associate vacancies, clinical operations careers, CRO jobs in India, GCP monitoring roles, clinical trial management jobs, pharmaceutical research careers, and healthcare clinical operations opportunities.

Candidates with strong knowledge of clinical trial processes, site monitoring, regulatory compliance, and clinical project coordination can apply for this opportunity.

Company Overview

Syngene is an innovation-led contract research, development, and manufacturing organization offering integrated scientific services from early discovery to commercial supply. The company supports pharmaceutical, biotechnology, healthcare, and research organizations through advanced scientific operations and clinical development services.

The organization operates extensively across clinical research, drug development, laboratory services, healthcare analytics, and contract research operations while maintaining strong quality, safety, and compliance standards.

Clinical research and clinical operations sectors continue to generate strong demand for professionals skilled in clinical trial monitoring, GCP compliance, site management, regulatory documentation, and healthcare project coordination.

Bangalore remains one of India’s leading hubs for CRO operations, biotechnology research, clinical development, pharmaceutical innovation, and healthcare technology services.

Job Role & Responsibilities

CRA – Clinical Operations Responsibilities

Candidates selected for this role will support clinical trial monitoring and site management activities.

Key responsibilities include:

• Performing site selection, initiation, monitoring, and close-out visits
• Managing assigned clinical study protocols and therapeutic areas
• Supporting site management and clinical trial coordination activities
• Conducting protocol and study-related training for assigned sites
• Establishing communication with study sites and investigators
• Ensuring compliance with GCP guidelines and clinical regulations
• Monitoring study quality and integrity at site level
• Investigating quality issues and supporting CAPA implementation
• Tracking regulatory and Ethics Committee submissions and approvals
• Monitoring subject recruitment and CRF completion activities
• Managing data query generation and resolution processes
• Preparing monitoring visit reports and follow-up documentation
• Supporting Clinical Project Managers with study tools and documentation
• Coordinating project activities and clinical operations workflows
• Supporting study timelines and regulatory compliance requirements

Skills Required

Candidates should possess:

• Strong clinical research knowledge
• Clinical trial monitoring expertise
• GCP and regulatory compliance understanding
• Site management and investigator coordination skills
• Clinical documentation and reporting abilities
• Communication and stakeholder management skills
• Problem-solving and analytical capabilities
• Attention to detail and organizational skills
• Ability to manage multiple study activities
• Understanding of CAPA and quality management processes

Candidates with exposure to CRO operations, therapeutic area monitoring, regulatory submissions, and healthcare compliance systems will have an advantage.

Eligibility / Qualifications

Educational Qualification

Candidates with healthcare and life sciences educational backgrounds are eligible.

Relevant educational qualifications include:

M.Pharm, MSc Life Sciences, MSc Pharmacology, Biotechnology, Clinical Research, Pharmaceutical Sciences, Healthcare Management.

Experience Requirement

• Hands-on experience in core clinical research activities required
• Clinical trial monitoring experience preferred
• Site management and GCP compliance exposure preferred
• CRO and clinical operations experience preferred

These openings are suitable for:

• Clinical Research Associates
• Clinical operations professionals
• CRO professionals
• GCP compliance specialists
• Site monitoring associates
• Clinical trial coordinators
• Healthcare research professionals

Location & Salary

Location

Bangalore, India

Estimated Salary

₹5.5 LPA – ₹11 LPA approximately

Salary may vary depending on clinical trial monitoring expertise, therapeutic area exposure, CRO experience, and GCP compliance knowledge.

Application Process

Interested candidates can apply through the official Syngene careers portal.

Apply Online

https://careers.syngeneintl.com/job/CRA/1361196266/

Department

Clinical Operations

Division

Discovery Services

Frequently Asked Questions (FAQs)

1. What position is Syngene hiring for in Bangalore?

Syngene is hiring for the role of CRA under Clinical Operations.

2. Which qualifications are eligible for this clinical research role?

Candidates with M.Pharm, MSc Life Sciences, MSc Pharmacology, Biotechnology, and Clinical Research qualifications can apply.

3. What experience is required for this CRA role?

Candidates with hands-on experience in core clinical research activities and clinical trial monitoring are preferred.

4. What skills are preferred for this opportunity?

Knowledge of GCP compliance, site management, clinical trial monitoring, CRF handling, and regulatory coordination is preferred.

5. What is the estimated salary for CRA positions at Syngene?

The expected salary range is approximately ₹5.5 LPA to ₹11 LPA depending on clinical research and monitoring experience.

6. What is the work location for this opportunity?

The work location is Bangalore, India.

Summary Table

Company	Syngene
Department Vacancies	CRA – Clinical Operations
Qualification	M.Pharm, MSc Life Sciences, MSc Pharmacology, Biotechnology, Clinical Research
Experience	Clinical Research & Monitoring Experience Preferred
Location	Bangalore, India

Tagged as: Pharma Jobs in Bangalore