Clinical Research Associate job at Sun Pharma Mumbai. Check eligibility, experience, responsibilities, and apply online for clinical research role today now.
Introduction
Are you an experienced clinical research professional aiming to advance your career with a leading pharmaceutical company? The Clinical Research Associate Job at Sun Pharma Laboratories Ltd offers a dynamic opportunity to work on clinical trials, site monitoring, and regulatory processes.
This role is ideal for candidates with prior clinical research experience who want to enhance their expertise in trial management, compliance, and global research standards.
Job Overview
| Details | Information |
|---|---|
| Job Title | Clinical Research Associate |
| Company Name | Sun Pharma Laboratories Ltd |
| Location | Mumbai, Maharashtra |
| Employment Type | Full-time |
| Department | Medical Affairs & Clinical Research |
| Experience Required | 1–5 Years |
| Education | Life Sciences / Pharmacy / Clinical Research |
| Salary | As per company standards |
Company Overview
Sun Pharma Laboratories Ltd is one of India’s largest pharmaceutical companies with a strong global presence. The organization is known for its focus on innovation, quality manufacturing, and clinical research excellence.
Working at Sun Pharma provides professionals with exposure to international clinical trial standards, regulatory frameworks, and advanced drug development processes.
Job Location & Employment Type
- Location: Mumbai (Sun House – Corporate Office)
- Employment Type: Full-time
- This role involves coordination with multiple clinical sites and stakeholders.
Open Positions / Department Details
- Role: Clinical Research Associate (CRA)
- Department: Medical Affairs & Clinical Research
- The role focuses on managing and monitoring clinical trials across multiple sites.
Key Roles & Responsibilities
As a Clinical Research Associate, your responsibilities will include:
Clinical Trial Management
- Conducting site feasibility assessments and identifying investigators
- Finalizing study sites and executing contracts (CDA, agreements)
- Coordinating site initiation, monitoring visits, and close-out activities
Regulatory & Compliance Activities
- Preparing and submitting documents for Ethics Committee (EC) approvals
- Ensuring compliance with Good Clinical Practice (GCP) guidelines
- Monitoring adherence to regulatory requirements
Site Monitoring & Data Management
- Overseeing investigational product (IP) handling, inventory, and reconciliation
- Ensuring accurate data entry, source data verification (SDV), and query resolution
- Monitoring recruitment timelines and study progress
Safety Reporting & Risk Management
- Reporting SAEs (Serious Adverse Events) and SUSARs as per regulations
- Identifying risks and implementing CAPA (Corrective and Preventive Actions)
- Ensuring compliance with pharmacovigilance policies
Coordination & Communication
- Training investigators and site staff on protocols and GCP
- Coordinating with CROs, data management, and statistical teams
- Supporting database lock (DBL) and final reporting
Eligibility Criteria
Education
Candidates must have:
- Bachelor’s or Master’s degree in:
- Biology
- Chemistry
- Pharmacy
- Nursing
- Public Health
- OR Postgraduate Diploma in Clinical Research
Experience
- Minimum 1–5 years of experience in clinical research
Skills Required
- Strong knowledge of clinical trial processes and GCP guidelines
- Site monitoring and trial management skills
- Excellent communication and coordination abilities
- Analytical thinking and problem-solving skills
- Attention to detail in documentation and compliance
- Ability to manage multiple sites and timelines
Salary & Benefits
- Salary: As per company standards
- Opportunity to work on global clinical trials
- Exposure to advanced research methodologies
- Career growth in clinical research and regulatory roles
- Learning opportunities in pharmacovigilance and data management
Selection Process
The hiring process may include:
- Resume shortlisting
- Technical interview (clinical research knowledge)
- HR discussion
- Final selection
How to Apply
- Candidates should apply through the official Sun Pharma careers portal.
- Ensure your CV highlights clinical research experience and relevant project exposure.
Important Dates
- Last date to apply: Not specified
Why Apply for This Job?
The Clinical Research Associate Job at Sun Pharma Laboratories Ltd is an excellent opportunity for professionals looking to grow in the clinical research domain.
Here’s why this role stands out:
- Work with a globally recognized pharmaceutical leader
- Hands-on experience in multi-site clinical trials
- Exposure to regulatory submissions and compliance
- Opportunity to handle end-to-end clinical trial processes
- Career progression into:
- Senior CRA
- Clinical Project Manager
- Regulatory Affairs Specialist
- Pharmacovigilance roles
FAQs
1. Who can apply for this Clinical Research Associate job?
Candidates with Life Science, Pharmacy, or Clinical Research qualifications and relevant experience can apply.
2. What is the required experience?
A minimum of 1–5 years of experience in clinical research is required.
3. What is the salary offered?
Salary is provided as per company standards.
4. What are the key responsibilities of a CRA?
Site monitoring, regulatory submissions, data verification, and trial coordination are key responsibilities.
5. How can I apply?
You can apply through the official Sun Pharma careers website.
Conclusion
The Clinical Research Associate Job at Sun Pharma Laboratories Ltd offers a strong career pathway for professionals in clinical research. With exposure to global trials, regulatory frameworks, and site management, this role can significantly enhance your professional growth.
If you have relevant experience and are ready for the next step in your clinical research career, this opportunity is worth applying for.
Disclaimer
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