Job Title: Clinical Trial Manager – Hyderabad
Location: Madhapur, Hyderabad, Telangana, India
Employment Type: Full-time
Job ID: 25103286
Syneos Health® is a fully integrated biopharmaceutical solutions organization, built to accelerate customer success. With expertise spanning clinical development, medical affairs, and commercial insights, we help clients bring innovative therapies to patients efficiently. Our Clinical Development model puts patients and customers at the center of everything we do, ensuring operational excellence and streamlined study execution.
Join our global team of 29,000 employees across 110 countries, and contribute to transforming patient care worldwide.
As a Clinical Trial Manager, you will oversee the planning, coordination, and execution of Phase 1 clinical research studies. You will serve as the primary liaison between investigators, research subjects, client teams, and clinic operations, ensuring studies are delivered on time, within budget, and in compliance with global and regional regulations.
This role requires meticulous resource planning, study logistics oversight, and progress tracking, while maintaining close alignment with project milestones and client deliverables.
Manage end-to-end Phase 1 clinical trial operations at Syneos Health facilities.
Act as the primary point of contact for investigators, study teams, and clients.
Plan and allocate study resources efficiently, ensuring adherence to budgets and timelines.
Monitor study progress, identify risks, and implement corrective actions to maintain compliance with regulatory requirements.
Collaborate with cross-functional teams including clinical operations, regulatory, and site staff.
Ensure thorough documentation and reporting of trial activities for client and regulatory review.
Support process improvements and contribute to the development of study protocols and operational strategies.
Advanced degree in Life Sciences, Pharmacy, or related field preferred.
Proven experience in clinical trial management, ideally within a CRO or pharmaceutical setting.
Knowledge of ICH-GCP guidelines, FDA, and EMA regulations.
Strong project management, communication, and organizational skills.
Ability to manage multiple studies and interact with global cross-functional teams effectively.
Work in a dynamic, innovative environment with global exposure.
Contribute to high-impact clinical trials advancing patient care.
Access opportunities for career development, mentorship, and professional growth.
Be part of a culture that values diversity, inclusion, and Total Self expression.
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