Sanofi Hiring for Central Clinical Research Associate
About Sanofi
Sanofi, a global leader in healthcare innovation, is committed to transforming scientific advancements into life-changing therapies. Join the team in Hyderabad and play a pivotal role in clinical research while contributing to impactful healthcare solutions. Sanofi Hiring for Central Clinical Research Associate
Job Title: Central Clinical Research Associate (CRA) – Registries
Location: Hyderabad, India
Experience Required: Minimum 3 Years
Salary: ₹7–9 LPA
Education: B.Pharm, M.Pharm, Pharm.D, MSc, BSc, or Life Sciences
Role Overview
- Employment Type: Permanent, Full-time
- Travel: As needed
This role involves comprehensive responsibilities across feasibility, site management, data collection, quality control, and stakeholder collaboration in clinical research.
Key Responsibilities
Feasibility & Site Selection
- Collaborate with the Registries Team to select study sites.
Study Start-Up
- Collect and review site documents for regulatory submissions.
- Customize informed consent forms and maintain documentation in eTMF.
Site Monitoring
- Conduct remote and occasional onsite visits for study initiation, monitoring, and close-out activities.
Data Management
- Review eCRF completeness, resolve data queries, and coordinate data collection projects.
Site Management
- Oversee patient recruitment, ensure adequate site facilities, and train staff on study protocols.
- Manage safety reporting and ensure compliance with study guidelines.
Quality Assurance
- Ensure adherence to Good Clinical Practice (GCP) and maintain audit readiness.
- Implement corrective actions as necessary.
Administrative Tasks
- Maintain study trackers, attend investigator meetings, and manage the investigator payment process.
Required Qualifications
Education
- A degree in pharmaceutical sciences or a life science-related field.
Experience
- Minimum of 3 years in clinical research, including trial monitoring.
- Experience in rare diseases or real-world evidence studies is advantageous.
Skills & Knowledge
- Proficient in GCP and regulatory guidelines (FDA, EMA).
- Strong understanding of data management and medical terminology.
Language Proficiency
- Fluent in English (spoken and written).
Preferred Skills
Technical Skills
- Attention to detail, technical writing, and project management.
- Experience with global projects and familiarity with registries.
Soft Skills
- Effective communication, adaptability, ethical judgment, and strong interpersonal skills.
How to Apply
Apply online through Sanofi’s career portal and become part of a company shaping the future of healthcare.
This is a unique opportunity to gain exposure to groundbreaking clinical research while working in a dynamic and supportive environment. Sanofi Hiring for Central Clinical Research Associate