Site Contract Specialist – Hyderabad | Syneos Health
Location: Hyderabad, India
Job ID: 25103283
Updated: November 14, 2025
Experience Required: 4–7 years in clinical site management or site start-up/contract negotiation
About Syneos Health
Syneos Health® is a fully integrated biopharmaceutical solutions organization dedicated to accelerating client success. We leverage unique clinical, medical affairs, and commercial insights to deliver outcomes aligned with modern healthcare challenges.
Our Clinical Development model centers on both the patient and client. By simplifying and streamlining processes, we make Syneos Health a premier partner for clients and an engaging workplace for employees.
Join a collaborative, innovative environment where passion drives the delivery of therapies that change lives globally.
Role Overview
The Site Contract Specialist will lead and manage the site identification and start-up process for clinical trials in Hyderabad, ensuring compliance with SOPs, regulations, and project requirements. This role serves as the primary liaison with investigative sites and oversees site agreements, site information forms, and site performance tracking.
This position requires an organized, detail-oriented professional capable of managing multiple priorities, negotiating site agreements, and ensuring high-quality start-up deliverables.
Key Responsibilities
Manage and execute site identification and initiation processes for clinical trials.
Negotiate and finalize site confidentiality agreements (CDAs) and site information forms (SIFs).
Maintain accurate tracking of site performance metrics, timelines, and deliverables.
Serve as the primary point of contact for investigative sites regarding contract, start-up, and compliance matters.
Review, approve, and submit documentation in line with internal SOPs and regulatory standards.
Collaborate with Clinical Operations, Project Management, and cross-functional teams to ensure smooth site activation.
Track completion of site identification activities and escalate issues or delays as necessary.
Participate in audits or regulatory inspections related to site start-up processes.
Contribute to process improvement initiatives for site management and start-up efficiency.
Required Qualifications & Experience
Education: Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related healthcare/clinical discipline.
Experience: 4–7 years in clinical site management, start-up, or clinical operations, preferably within Phase I–III trials.
Proven experience in site contracts, negotiations, and clinical site documentation.
Strong knowledge of ICH-GCP, local regulatory requirements, and clinical trial processes.
Excellent communication, negotiation, and stakeholder management skills.
Ability to manage multiple sites and deliverables simultaneously.
Experience with clinical trial management systems and electronic site tracking tools is preferred.
Why Syneos Health?
Join a global team of 29,000 employees across 110 countries.
Contribute to clinical trials that have impacted 94% of FDA-approved novel drugs and 95% of EMA-authorized products in the last five years.
Opportunities for career growth, professional development, and cross-functional mentorship.
Inclusive, supportive work culture that values diversity, collaboration, 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 all local and global regulations, including the Americans with Disabilities Act.
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