Clinical Trial Manager (Hyderabad)

Syneos Health

6-10 years

Not Disclosed

Hyderabad India

10 Nov. 28, 2025

Job Description

Job Type: Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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 – Hyderabad | Syneos Health

Location: Hyderabad, India (Hybrid)
Job ID: 25103286
Updated: November 6, 2025
Experience Required: 6–10 years in clinical trial management, preferably in Phase I–III trials

About Syneos Health

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating client success. We transform unique clinical, medical affairs, and commercial insights into actionable outcomes that address modern healthcare challenges.

Our Clinical Development model places the patient and client at the center of everything we do. By continuously simplifying and streamlining processes, we ensure Syneos Health is both easier to work with and a rewarding workplace for our teams.

Join a collaborative environment where innovation, agility, and passion drive the delivery of therapies that change lives globally.

Role Overview

The Clinical Trial Manager (CTM) will oversee the planning, execution, and completion of clinical studies at Syneos Health’s Hyderabad operations. This role is responsible for ensuring clinical trials are conducted on time, within budget, and in full compliance with regulatory requirements.

As a CTM, you will serve as the primary liaison between internal teams, clients, investigators, and site staff while managing study logistics, monitoring progress, and driving continuous improvement in trial operations.

Key Responsibilities

Lead the planning, coordination, and management of Phase I–III clinical trials.
Oversee study operations, including subject recruitment, site management, and compliance with protocol and regulatory requirements.
Serve as primary contact for investigators, study teams, and clients, facilitating effective communication and resolution of issues.
Monitor study timelines, milestones, budgets, and deliverables to ensure successful completion.
Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements.
Develop and maintain study documentation, including study plans, monitoring reports, and trial master files.
Coordinate cross-functional teams, including Clinical Operations, Biostatistics, Data Management, and Medical Affairs.
Provide mentorship and guidance to junior staff, fostering professional development.
Participate in internal and external audits, as required.
Contribute to process improvement initiatives to optimize operational efficiency and quality standards.

Required Qualifications & Experience

Education: Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or related healthcare/clinical discipline.
Experience: 6–10 years in clinical trial management, with demonstrated expertise in Phase I–III trials.
Proven ability to manage multiple studies, budgets, and project timelines effectively.
Strong knowledge of GCP, ICH guidelines, and local regulatory requirements.
Excellent communication, leadership, and stakeholder management skills.
Experience collaborating with cross-functional teams and external vendors.
Familiarity with electronic trial management systems and clinical databases is preferred.

Why Syneos Health?

Work with a global team of 29,000 employees across 110 countries.
Contribute to studies that have impacted 94% of FDA-approved novel drugs and 95% of EMA-authorized products in the past five years.
Opportunities for career growth, professional development, and mentoring.
A culture of authenticity, inclusivity, and recognition.

Additional Information

Tasks and responsibilities are not exhaustive. Syneos Health may assign additional duties based on business needs. Equivalent experience or qualifications may be considered. Syneos Health is committed to equal employment opportunities and compliance with local and global regulations, including the Americans with Disabilities Act.

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Clinical Trial Manager (Hyderabad)

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