Central Clinical Research Associate (CRA)
About the Role
Company Description
Sanofi Business Operations, or SBO, is an internal team based in India that supports Sanofi's work worldwide. It centers processes for Specialty Care, Vaccines, General Medicines, and other key areas, along with R&D and Digital functions. SBO works closely with Medical, HEVA, and Commercial teams and helps reduce dependence on outside service providers. It focuses on building strong skills within the company itself.
Job Summary
This role is based in Sanofi’s Registries team, which's part of the General Medicines function in Hyderabad. Central Clinical Research Associate will be the point of contact between the Principal Investigator and site staff for rare disease registries. You are expected to support the study process by managing communication and ensuring that all required information flows correctly. This position plays a role in maintaining the quality and consistency of data across sites.
Key Responsibilities
Support site selection along with the registries team.
Help collect and check documents needed for regulatory and ethics submissions.
Assist with site contracts, budgets, and consent form updates for each country.
Upload and manage study documents in the eTMF system.
Plan and carry out site visits, both remote and on-site, following GCP guidelines.
Review study data and follow up on missing or unclear information.
Support patient enrollment and monitor patient status throughout the study.
Make sure sites have proper staff, training, and system access.
Support safety reporting and help maintain audit readiness at the site level.
Keep trackers, databases, and reports updated and accurate.
Take part in study meetings, training sessions, and quality reviews.
Build and maintain strong working relationships with investigators and other stakeholders.
Educational Qualification and Skills Required
Degree in pharmacy, life sciences, or a related scientific field.
At least 5 years of experience in clinical research, including trial monitoring.
Experience with rare diseases or real world evidence studies is a plus.
Strong attention to detail and solid problem solving skills.
Good project management skills, including handling timelines and resources.
Skilled in writing clear reports, protocols, and regulatory documents.
Comfortable working on global projects with teams across different countries.
Strong understanding of GCP guidelines and regulatory requirements.
Good working knowledge of medical terms and clinical trial processes.
Comfortable using Microsoft Office and clinical data systems.
High level of proficiency in written and spoken English.
Salary Structure
The estimated average salary for a Central Clinical Research Associate (Central CRA) at Sanofi ranges between ₹12.0 Lakhs and ₹19.2 Lakhs per year, depending on the required experience level.
Career Development
This role gives you hands-on experience with every part of the clinical trial process. You'll work through site selection then move into trial execution and finally help with close out. Over time, it opens the door to more advanced roles in clinical research and study management within Sanofi.
How to Apply
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Market Insights & Trends
Salary Insights
The amount of money that gets paid can be different depending on how they have been working, where they live and what kind of job they are doing. Some places pay more than others. Most good jobs include extra money for doing a good job, health insurance and flexible hours. Companies pay high salary to make sure they can get the people they want.
Hiring Trends
The number of jobs for this profile is going up every year. Hospitals and other healthcare companies are looking for people who're good, at their job and can also figure out new problems. They want who can do the work and also think on their feet to deal with the challenges of working in healthcare today.