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Clinical Trial Manager I

3+ years
Not Disclosed
10 Nov. 11, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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