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Centralized Study Analyst

Fortrea
3-4 years
INR 6-10LPA
Hyderabad, Pune, India
10 June 16, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, 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

Key Responsibilities

1. Clinical Trial Contract Management

  • Draft, review, negotiate, and finalize:

    • Clinical Trial Agreements (CTAs)

    • Confidentiality Agreements (CDAs/NDAs)

    • Contract Amendments

    • Related Site Contract Documentation

  • Coordinate with Sponsors, Legal Teams, Clinical Operations, and Study Teams for timely contract execution.

  • Manage site agreement timelines and ensure completion within study milestones.

  • Facilitate internal approval workflows and obtain required authorizations.

  • Track contract execution status and maintain accurate documentation in SAMS, UCV, and other applicable systems.

  • Ensure executed agreements are filed and archived appropriately.


2. Protocol Amendment Management

  • Coordinate protocol amendment submissions and associated documentation updates.

  • Support amendment-related contract and budget revisions.

  • Review amendment requirements and communicate action items to sites and study teams.

  • Track amendment progress and ensure timely completion of:

    • Submissions

    • Approvals

    • Implementation activities

  • Maintain amendment documentation in applicable systems and trackers.

  • Support site communications and resolve outstanding amendment-related queries.


3. Stakeholder & Cross-Functional Collaboration

  • Collaborate with:

    • Clinical Operations

    • Regulatory Affairs

    • Legal Teams

    • Finance Teams

    • Sponsors and Study Teams

  • Provide regular updates on contract and amendment status.

  • Support efficient study start-up and ongoing study execution.


4. Risk Management & Escalation

  • Proactively identify contracting risks, delays, and operational challenges.

  • Escalate issues to management when required.

  • Monitor study deliverables and mitigate potential timeline impacts.


5. Compliance & Quality

  • Ensure compliance with:

    • ICH-GCP Guidelines

    • SOPs

    • Sponsor Requirements

    • Regulatory Standards

  • Maintain audit-ready documentation.

  • Support inspections and audits.

  • Complete required training, compliance activities, and timesheets within deadlines.


6. Reporting & Process Improvement

  • Maintain study trackers, metrics, and reports.

  • Generate status updates for management and project teams.

  • Participate in process improvement initiatives.

  • Support departmental objectives and quality enhancement programs.


Required Skills & Competencies

Technical Skills

  • Clinical Trial Contracting

  • Site Agreement Negotiation

  • Protocol Amendments

  • Study Start-Up Activities

  • Clinical Research Operations

  • ICH-GCP Compliance

  • Contract Tracking Systems

  • Microsoft Office Suite

Soft Skills

  • Excellent Communication Skills

  • Negotiation Skills

  • Stakeholder Management

  • Attention to Detail

  • Time Management

  • Organization & Prioritization

  • Problem Solving

  • Team Collaboration


Educational Qualification

  • Bachelor's Degree in Life Sciences, Pharmacy, Biotechnology, Nursing, Medical Laboratory Technology, or related healthcare field.

  • Equivalent relevant experience may be considered in lieu of formal education.


Potential Job Titles

  • Clinical Trial Contract Specialist

  • Site Contract Specialist

  • Study Start-Up Specialist

  • Clinical Contracts Associate

  • Clinical Trial Agreements Specialist

  • Site Activation Specialist

  • Start-Up & Contracts Specialist

  • Clinical Operations Contracts Specialist