Syneos Health, a global leader in biopharmaceutical solutions, is inviting applications for the position of Clinical Research Associate II (Client base) in Mumbai, India. This hybrid opportunity offers professionals in clinical research a chance to contribute to impactful studies while working with one of the most respected names in the CRO industry.
If you have a passion for clinical monitoring, patient safety, and regulatory compliance, this is your opportunity to grow your career with an organization committed to innovation and development.
About Syneos Health
Syneos Health® is a fully integrated biopharmaceutical solutions organization that supports the clinical development, commercialization, and market success of new therapies. With over 29,000 employees across 110 countries, Syneos Health is dedicated to accelerating the delivery of life-changing treatments through collaboration, technology, and patient-centered approaches.
Key Responsibilities
As a Clinical Research Associate II, your main duties include:
- Overseeing the progress of clinical trials and ensuring adherence to protocols, SOPs, and GCP guidelines.
- Acting as the site-level liaison for internal and external stakeholders.
- Identifying and assessing potential investigators and sites for new studies.
- Conducting pre-study, initiation, monitoring, and close-out visits.
- Reviewing site activities, data quality, and safety reporting.
- Managing multiple protocols across therapeutic areas while maintaining compliance and timelines.
- Providing training and mentorship to site staff and maintaining effective relationships.
- Supporting audit and inspection readiness by ensuring corrective and preventive actions are implemented.
Required Qualifications
- Bachelor’s degree (preferably in Life Sciences) or equivalent combination of education and experience.
- Minimum 3 years of clinical research experience with at least 1 year of on-site monitoring.
- Strong knowledge of ICH-GCP guidelines, clinical trial regulations, and clinical research methodologies.
- Excellent communication, time management, and organizational skills.
- Proficiency in electronic data capture (EDC) and clinical trial management systems (CTMS).
- Willingness to travel up to 75% of the time.
Preferred Qualifications
- Experience working with Pharma or Biotech sponsors or as a Clinical Study Coordinator.
- Familiarity with regulatory compliance, ethics committee submissions, and investigator site file (ISF) management.
Why Join Syneos Health
- Opportunity to work with a leading global CRO known for innovation and excellence.
- Hybrid work model with flexibility and support for work-life balance.
- Professional development, continuous learning, and career progression programs.
- Inclusive “Total Self” culture, celebrating diversity, authenticity, and well-being.
- Competitive compensation and comprehensive benefits.
How to Apply
