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Clinical Trial Manager I

2-3 years
Not Disclosed
10 Oct. 19, 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

📅 Updated: October 16, 2025
📍 Location: India (Client Site)
🆔 Job ID: 25102351


Company Overview

Syneos Health® is a fully integrated biopharmaceutical solutions organization, committed to accelerating customer success. The company brings together clinical, medical affairs, and commercial expertise to improve outcomes for patients and simplify processes for clients.

Culture & Values:

  • Focused on career development, technical and therapeutic training, and peer recognition.

  • Promotes a Total Self culture to encourage authenticity, inclusion, and belonging.

  • Emphasizes collaboration, innovation, and agility to accelerate therapy delivery.

Impact Statistics:

  • Worked with 94% of novel FDA-approved drugs, 95% EMA-authorized products, and over 200 studies across 73,000 sites involving 675,000+ trial patients.


Job Purpose

Oversee the development, coordination, and execution of Phase 1 clinical research studies, ensuring alignment with regulatory standards, project milestones, client deliverables, and budgets. Serve as a liaison between investigators, research subjects, client teams, and clinic operations. Contribute to process, program, and policy design to ensure clinical trials are conducted efficiently and effectively.


Key Responsibilities

Clinical Trial Management

  • Develop and coordinate Phase 1 clinical research studies from planning to execution.

  • Implement clinical research protocols and ensure compliance with Good Clinical Practice (GCP) guidelines.

  • Collaborate with principal investigators, research subjects, client teams, and clinic operations teams for smooth coordination.

  • Plan and manage logistics, resources, scheduling, budgeting, and resource allocation for clinical trials.

  • Track study progress, ensuring alignment with project milestones, client deliverables, and budgets.

  • Prepare and present study reports and updates to stakeholders, including detailed analysis of study data.

  • Provide guidance and support to junior professionals, fostering collaboration.

  • Identify and resolve study-related challenges promptly and effectively.

  • Maintain accurate and comprehensive documentation of all study activities.

Regulatory & Compliance

  • Ensure adherence to global and regional regulations and guidelines.

  • Stay updated on changes in regulatory requirements relevant to clinical trials.

Process Improvement & Contribution

  • Contribute to the design, implementation, and delivery of clinical processes, programs, and policies.

  • Manage and potentially direct the work of lower-level professionals to ensure efficient execution of trials.


Qualifications

  • Education: Bachelor’s degree in Life Sciences, Clinical Research, or related field.

  • Experience:

    • Minimum 3 years in clinical trial management or related field.

    • Minimum 2 years of project management experience.

    • Experience in global pharma is preferred.

    • Candidate from Mumbai location preferred.

  • Knowledge & Skills:

    • In-depth understanding of clinical research processes and regulations.

    • Strong project management and organizational skills.

    • Excellent communication and interpersonal skills.

    • Ability to work independently and in teams.

    • Proficiency with clinical trial management software and tools.

    • Strong analytical and problem-solving skills, attention to detail, ability to manage multiple projects.

    • Knowledge of GCP guidelines and regulatory requirements.

  • Certifications: Certified Clinical Research Professional (CCRP) or equivalent preferred.

  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).


Impact & Contribution

  • Ensure all aspects of Phase 1 trials are meticulously planned and executed.

  • Significantly influence trial success and contribute to medical research and new treatment development.


Additional Information

  • This posting may represent a potential future opportunity, not a live role.

  • Tasks, duties, and responsibilities may evolve based on company discretion.

  • Transferrable skills and equivalent experience may be considered.

  • Commitment to compliance with applicable legislation and regulations.

  • Reasonable accommodations provided under the Americans with Disabilities Act when appropriate.


Company Commitment to Inclusion

  • Encourages applicants from diverse backgrounds to apply, even if experience doesn’t match perfectly.

  • Join the Talent Network to stay informed about additional opportunities.

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