Clinical Trial Manager I – Syneos Health
Location: IND – Client
Job ID: 25102784
Updated: November 4, 2025
✅ About Syneos Health
Syneos Health® is a global, fully integrated biopharmaceutical solutions provider helping customers accelerate the delivery of therapies.
29,000 employees across 110 countries
Supported 94% of FDA-approved Novel Drugs and 95% of EMA-authorized products
Involved in 200+ studies, 73,000 sites, 675,000+ patients
The company promotes innovation, collaboration, continuous learning, and its “Total Self” culture—encouraging authenticity, diversity, and belonging.
✅ Role Overview
The Clinical Trial Manager I (CTM I) manages and coordinates Phase I–IV clinical research studies, ensuring proper planning, execution, compliance, and delivery of all study-related activities.
This role works closely with investigators, clients, clinical teams, and operations to ensure study success.
✅ Key Responsibilities
1. Study Management & Execution
Develop, plan, and coordinate Phase I–IV clinical trials end-to-end.
Implement clinical protocols while ensuring compliance with GCP, regulatory guidelines, and study requirements.
Oversee study timelines, quality metrics, deliverables, and budget adherence.
2. Cross-Functional Collaboration
Act as the primary liaison for:
Principal investigators
Research subjects
Client teams
Clinic operations teams
Facilitate effective communication between all stakeholders.
3. Operational Planning
Manage trial logistics, including:
Visit scheduling
Resource allocation
Budget planning
Vendor coordination
Monitor progress to ensure milestones and deliverables are achieved.
4. Compliance & Quality Oversight
Ensure all trial activities follow:
ICH-GCP
Global and regional regulatory requirements
Internal SOPs
Identify non-compliance issues and implement corrective actions.
5. Documentation & Reporting
Maintain accurate and complete study documentation.
Prepare and present study progress reports to stakeholders.
Analyze data trends and provide insights on study performance.
6. Issue Resolution
Proactively identify operational challenges and implement effective solutions.
Address escalating issues to ensure uninterrupted study execution.
7. Leadership & Team Support
Provide guidance and mentoring to junior team members.
Foster a collaborative and supportive team environment.
✅ Qualifications
Education
Bachelor’s degree in Life Sciences, Clinical Research, or related field.
Experience
Minimum 3 years of experience in clinical trial management or related operational roles.
Knowledge & Skills
Strong understanding of:
Clinical research processes
Regulatory requirements
Good Clinical Practice (GCP)
Proficient in:
Clinical Trial Management Systems (CTMS)
Microsoft Office (Excel, Word, PowerPoint)
Excellent communication, organizational, and interpersonal skills.
Ability to manage multiple studies and priorities simultaneously.
Strong analytical and problem-solving skills.
Certifications (Preferred)
CCRP (Certified Clinical Research Professional) or equivalent.
✅ Role Summary (P22 Level)
Roles at the P22 level involve:
Overseeing development and coordination of Phase I clinical research studies
Acting as liaison between research subjects, investigators, clients, and clinic teams
Managing logistics, resource planning, and compliance
Contributing to clinical operations processes, policies, and improvements
Potentially supervising lower-level team members
Ensuring trials are executed efficiently, accurately, and in accordance with global regulations
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Rangpo |India :
Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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