Sanofi Hiring for Clinical Research Associate in Hyderabad
Company: Sanofi
Position: Central CRA (Clinical Research Associate) – Registries
Job Type: Permanent, Full-Time
Location: Hyderabad, India
Experience Required: 3+ Years
Salary Range: ₹7 – ₹8 LPA
Educational Qualification: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Lifesciences
Application Mode: Online
Job Status: Verified Job Posting
About Sanofi
Sanofi is a global biopharmaceutical company focused on human health. With a legacy of scientific innovation and global reach, Sanofi is committed to transforming medical research into life-changing treatments. The company specializes in therapeutic areas such as rare diseases, oncology, immunology, vaccines, and general medicines. Sanofi provides a dynamic and inclusive work environment that nurtures talent, encourages continuous learning, and promotes patient-centered outcomes. Sanofi Hiring for Clinical Research Associate
Sanofi is currently hiring for the position of Central Clinical Research Associate (CRA) for their Registries Division in Hyderabad, offering a promising career opportunity in clinical trial operations.
Job Overview
Job Title: Central CRA (Clinical Research Associate) – Registries
Location: Hyderabad, India
Department: Clinical Operations
Job Type: Full-Time, Permanent
Annual Salary: ₹7,00,000 – ₹8,00,000 (depending on experience)
Key Responsibilities
Feasibility and Start-Up Activities:
- Participate in site feasibility assessments and site selection in coordination with project teams.
- Prepare and submit documents to Health Authorities and Ethics Committees for regulatory approvals.
- Coordinate and manage site contracts, budget negotiations, and insurance documentation.
- Ensure the customization and proper review of Informed Consent Forms (ICFs) in compliance with regulatory standards.
- Sanofi Hiring for Clinical Research Associate
Monitoring and Site Management:
- Conduct remote and onsite monitoring visits including site initiation, interim monitoring, and site close-out.
- Review source data, resolve queries, and ensure adherence to protocols and Good Clinical Practice (GCP) guidelines.
- Ensure that all assigned trial sites operate in full compliance with clinical protocols, regulatory standards, and internal SOPs.
Data and Safety Management:
- Maintain quality control over clinical data during trial execution.
- Monitor safety reporting processes and ensure timely communication of safety events.
- Identify protocol deviations and implement Corrective and Preventive Actions (CAPAs) where necessary.
- Support audit readiness and assist during regulatory inspections.
Administration and Documentation:
- Maintain trackers, logs, and clinical trial management systems to monitor study milestones.
- Ensure that all required documents are accurately maintained in the Trial Master File (TMF) and are audit ready.
- Participate in investigator meetings, internal trainings, and quality assurance activities.
Stakeholder Engagement:
- Collaborate with investigators, study coordinators, sponsors, and regulatory authorities.
- Act as the communication bridge between internal and external stakeholders to ensure study progress.
- Resolve conflicts or operational delays and provide timely updates on key deliverables.
Required Qualifications
Educational Background:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Medical Sciences, or other related scientific disciplines.
- Pharm.D, M.Sc, or equivalent qualifications in health-related domains are acceptable.
Professional Experience:
- Minimum 3 years of experience in clinical research or trial monitoring roles.
- Prior experience in real-world evidence, observational studies, or rare disease studies is advantageous.
- Familiarity with international regulatory environments and global clinical trials is highly desirable.
Technical Proficiency:
- Solid understanding of GCP (Good Clinical Practice), ICH guidelines, and regulatory frameworks.
- Working knowledge of data management systems, clinical trial documentation, and safety reporting tools.
- Proficiency in Microsoft Office applications, especially Excel, Word, and PowerPoint.
- Sanofi Hiring for Clinical Research Associate
Soft Skills:
- Strong communication skills, both written and verbal.
- Proven problem-solving abilities and ethical judgment.
- Highly organized with effective time management and multi-tasking capabilities.
- Excellent interpersonal skills to manage complex stakeholder relationships.
Why Join Sanofi?
Sanofi offers a unique opportunity to contribute to groundbreaking research in a collaborative and inclusive environment. The organization provides: Sanofi Hiring for Clinical Research Associate
- A culture focused on scientific excellence and ethical conduct.
- Exposure to international clinical trial operations and best practices.
- Opportunities for career development, training, and advancement.
- Competitive salary packages and health & wellness benefits.
- A commitment to employee well-being, diversity, and professional growth.
Application Deadline
Apply by: July 31, 2025
Eligible candidates are encouraged to submit their applications as early as possible to be considered for this opportunity.
How to Apply
Interested candidates can apply online via the official Sanofi Careers portal or recruitment page. Ensure your resume is updated with relevant clinical trial experience and your contact details. Shortlisted candidates will be contacted for further evaluation and interview rounds. Sanofi Hiring for Clinical Research Associate
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