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Clinical Trial Manager I

3+ years
Not Disclosed
10 Oct. 28, 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: IND – Client-Based
Job ID: 25102351
Company: Syneos Health®


About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization that accelerates customer success by combining clinical, medical affairs, and commercial expertise.

Our Clinical Development model places both the customer and patient at the center of everything we do. With a presence in 110 countries and a team of 29,000+ professionals, we continuously simplify and streamline operations to make Syneos Health not only easier to work with — but easier to work for.

Work Here Matters Everywhere.


Why Join Us

  • Career development and progression opportunities.

  • Supportive and engaged leadership.

  • Technical and therapeutic training programs.

  • Peer recognition and total rewards.

  • A Total Self Culture where authenticity, diversity, and inclusion thrive.

At Syneos Health, we bring together diverse perspectives to create a workplace where everyone feels they belong and can grow.


Position Summary

The Clinical Trial Manager I will oversee the development, coordination, and implementation of Phase I clinical research studies. This includes ensuring regulatory compliance, managing resources, tracking progress, and liaising between investigators, client teams, and operations staff.

This role plays a vital part in ensuring that studies are conducted efficiently, on time, and in alignment with global standards.


Experience Required

  • Minimum 2 years of project management experience.

  • Global pharmaceutical experience required.

  • Candidates from Mumbai preferred.


Key Responsibilities

  • Develop, coordinate, and manage Phase I clinical trials, ensuring meticulous planning and execution.

  • Implement study protocols and ensure adherence to GCP (Good Clinical Practice) and regulatory standards.

  • Serve as a liaison between principal investigators, clients, and clinic operations teams.

  • Manage logistics, scheduling, and budget/resource allocation for ongoing trials.

  • Track and report study progress against project milestones and deliverables.

  • Prepare and present study progress reports and data analyses to stakeholders.

  • Ensure compliance with global and regional regulations.

  • Support and mentor junior professionals to promote a collaborative work environment.

  • Identify and resolve study-related challenges efficiently.

  • Maintain comprehensive documentation for all study activities.


Qualifications

  • Bachelor’s degree in Life Sciences, Clinical Research, or related discipline.

  • Minimum 3 years of experience in clinical trial management or equivalent.

  • Strong understanding of clinical research processes and global regulations.

  • Excellent project management, organizational, and interpersonal skills.

  • Ability to manage multiple priorities and deadlines.

  • Proficiency in clinical trial management systems (CTMS) and Microsoft Office Suite.


Preferred Certifications

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


Core Skills & Competencies

  • Strong analytical and problem-solving ability.

  • Excellent written and verbal communication skills.

  • Attention to detail and accuracy.

  • Proactive and collaborative team player.

  • Thorough understanding of GCP guidelines and global compliance requirements.


Impact & Contribution

As part of the Clinical Trial Management (P22) job family, this role contributes significantly to the success of early-phase studies by:

  • Overseeing the planning and coordination of clinical research activities.

  • Ensuring compliance and quality throughout the trial lifecycle.

  • Supporting the design, implementation, and delivery of efficient clinical processes.

  • Managing and mentoring team members to enhance performance and productivity.


About Syneos Health’s Global Impact

Over the past 5 years, Syneos Health has partnered with:

  • 94% of all Novel FDA-Approved Drugs

  • 95% of EMA-Authorized Products

  • 200+ Clinical Studies across 73,000 Sites and 675,000+ Trial Patients

Join us and make a global impact in advancing life-changing therapies.


Additional Information

  • The company may modify job duties or responsibilities as needed.

  • Equivalent education, experience, or skills may be considered.

  • Syneos Health is an Equal Opportunity Employer, compliant with ADA and international equality directives.


Apply Now

🔗 www.syneoshealth.com

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