Clinical Trial Manager I
Job ID: 25102784
Updated: November 4, 2025
Location: Pune, Maharashtra, India
Company: Syneos Health®
Job Type: Full-time
About Syneos Health
Syneos Health® is a fully integrated biopharmaceutical solutions organization committed to accelerating customer success. We bring together clinical, medical affairs, and commercial insights to deliver real-world outcomes and address evolving market needs.
Our Clinical Development model centers around the customer and patient, simplifying processes to make Syneos Health easier to work with—and work for. Whether you join us in a Functional Service Provider (FSP) partnership or Full-Service environment, you’ll collaborate with dedicated professionals who are passionate about innovation, problem-solving, and improving patient lives.
With 29,000 employees across 110 countries, we embody our mission that—
“WORK HERE MATTERS EVERYWHERE.”
Why Join Syneos Health
Career development and growth opportunities
Supportive and engaged line management
Continuous learning through technical and therapeutic training
Peer recognition and total rewards programs
Inclusive “Total Self Culture”—encouraging authenticity, diversity, and belonging
A global environment where every perspective is valued
Job Responsibilities
Study Development & Coordination
Lead the planning, development, and execution of Phase I–IV clinical research studies.
Ensure study protocols comply with ICH-GCP, regulatory requirements, and internal SOPs.
Collaborate with principal investigators, client teams, and clinic operations to coordinate study activities and ensure seamless communication.
Operational Management
Manage logistics, resources, and budgets for assigned clinical trials.
Oversee scheduling, milestone tracking, and resource allocation to ensure studies stay within scope, timeline, and cost.
Prepare and deliver progress reports and data analysis summaries to internal and external stakeholders.
Regulatory Compliance & Quality Oversight
Ensure adherence to global and regional clinical research regulations.
Maintain up-to-date knowledge of regulatory updates and industry best practices.
Promote data accuracy, protocol adherence, and patient safety across all study phases.
Leadership & Team Collaboration
Provide guidance, mentorship, and oversight to junior clinical operations staff.
Foster a collaborative team environment that encourages transparency, accountability, and knowledge sharing.
Identify and resolve study-related issues proactively through effective problem-solving.
Documentation & Reporting
Maintain accurate, comprehensive, and audit-ready documentation of all study activities.
Ensure all study-related communications, reports, and records meet company and sponsor standards.
Qualifications
Bachelor’s degree in Life Sciences, Clinical Research, or a related field
Minimum 3 years of experience in clinical trial management or equivalent role
Strong understanding of clinical research processes, GCP guidelines, and regulatory compliance
Proven project management, leadership, and organizational abilities
Excellent communication and interpersonal skills
Proficiency in clinical trial management systems (CTMS) and related tools
Preferred Certifications
Certified Clinical Research Professional (CCRP) or equivalent credential (preferred but not mandatory)
Essential Skills
Analytical thinking and problem-solving abilities
Strong attention to detail and documentation accuracy
Ability to manage multiple concurrent projects and priorities
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
In-depth understanding of Good Clinical Practice (GCP) and regulatory frameworks
Impact & Contribution
Roles within the Clinical Trial Management job family at the P22 level play a pivotal role in ensuring the successful planning and execution of clinical research studies.
They:
Coordinate all operational aspects of clinical trials
Serve as the liaison between investigators, clients, and internal teams
Ensure compliance with global and regional regulations
Contribute to designing and implementing key clinical processes and programs
Manage project timelines, deliverables, and team performance
By directing resources efficiently and maintaining compliance, these professionals directly advance medical research and the development of innovative therapies.
About Syneos Health’s Global Impact
Partnered in 94% of all FDA-approved novel drugs in the past five years
Supported 95% of EMA-authorized products
Managed 200+ studies, across 73,000 sites and 675,000+ patients worldwide
Learn more at 👉 www.syneoshealth.com
Additional Information
Job responsibilities and duties may evolve per company needs.
Equivalent education or experience may substitute listed qualifications.
Syneos Health complies with all equal employment and disability accommodation laws, including the Americans with Disabilities Act (ADA).
This description does not constitute a binding employment contract.
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