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Site Contract Specialist (Hyderabad)

0-2 years
Not Disclosed
10 Nov. 11, 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

Site Contract Specialist – Hyderabad

Company: Syneos Health
Location: Hyderabad, India
Job ID: 25103283
Updated: November 6, 2025


About Syneos Health

Syneos Health® is a fully integrated biopharmaceutical solutions organization that supports clients across Clinical Development, Medical Affairs, and Commercial operations.

  • 29,000 employees across 110 countries

  • Worked on 94% of FDA-approved Novel Drugs and 95% of EMA-authorized products in the last 5 years

  • Over 200+ studies, 73,000 sites, and 675,000+ trial patients

Syneos focuses on creating a workplace where people grow professionally, feel valued, and contribute meaningfully through innovation and collaboration.


Role Summary

The Site Contract Specialist works within the Site Start-Up/Site Identification team and is responsible for supporting the activation of clinical trial sites.
This includes managing documentation, negotiating confidentiality agreements, and acting as the main contact for investigative sites.


Key Responsibilities

1. Site Identification & Start-Up

  • Execute and manage the site identification process as per regulations, SOPs, and study requirements.

  • Ensure timely completion of Site Information Forms (SIFs) and Confidentiality Agreements (CDAs).

2. Contract Review & Negotiation

  • Review, negotiate, and finalize site-level confidentiality agreements with investigators/sites.

  • Coordinate with internal teams to ensure contract timelines are met.

3. Stakeholder Management

  • Act as the primary point of contact for all assigned investigative sites.

  • Collaborate with project teams, site management teams, and study stakeholders.

4. Reporting & Metrics

  • Maintain and track site performance metrics, timelines, and site-readiness reports.

  • Regularly update systems with accurate site documentation and progress status.

5. Compliance

  • Ensure all activities comply with ICH-GCP, regulatory guidance, company SOPs, and study-specific requirements.

6. Additional Duties

  • Support related tasks as assigned by management.

  • Participate in process improvements within Site Start-Up.


Who Succeeds in This Role

This role suits individuals who:

  • Have practical knowledge in clinical research operations

  • Communicate clearly with internal teams and external sites

  • Understand regulatory and clinical documentation

  • Can independently manage multiple sites and timelines

  • Have strong organizational and negotiation skills


Position Type

  • Individual Contributor (Professional/Technical discipline)

  • May guide junior team members

  • Manages defined project components within Site Start-Up


Company Commitment

Syneos Health is committed to:

  • Diversity, equity & inclusion

  • ADA compliance & reasonable accommodations

  • Providing career development, training, and recognition

  • A culture where people can be their Total Self