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Regulatory And Start-Up

Fortrea
3-5 years
INR 6-10 LPA
Bangalore, 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, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS, 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

    • Site Contract Documentation

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

  • Ensure timely contract completion according to study milestones and turnaround timelines.

  • Facilitate contract approvals and obtain required authorizations.

  • Track contract execution status and maintain contract repositories.

  • Maintain accurate contract records within:

    • SAMS

    • UCV

    • Other Contract Management Systems


2. Protocol Amendment Management

  • Coordinate protocol amendment submissions and related documentation updates.

  • Support contract and budget revisions resulting from protocol amendments.

  • Review amendment requirements and communicate timelines and deliverables to stakeholders.

  • Track amendment progress and ensure timely:

    • Submission

    • Approval

    • Implementation

  • Ensure amendment documentation is complete and properly maintained.


3. Stakeholder & Cross-Functional Collaboration

  • Partner with:

    • Clinical Operations

    • Regulatory Affairs

    • Legal Teams

    • Finance Teams

    • Sponsors

    • Study Teams

  • Support efficient contract negotiation and amendment execution.

  • Communicate study status updates and outstanding issues to stakeholders.

  • Coordinate site communications and follow-up activities.


4. Contract Tracking & Documentation Management

  • Maintain accurate study trackers and status reports.

  • Ensure executed agreements are filed appropriately.

  • Monitor key contract metrics and timelines.

  • Maintain complete documentation for audit readiness.

  • Ensure data accuracy within tracking systems and repositories.


5. Risk Management & Escalation

  • Identify:

    • Contracting Risks

    • Timeline Delays

    • Operational Challenges

    • Compliance Issues

  • Escalate critical risks to management promptly.

  • Support issue resolution activities to minimize study impact.

  • Monitor study deliverables and contractual obligations.


6. Compliance & Quality Assurance

  • Ensure compliance with:

    • ICH-GCP Guidelines

    • Sponsor Requirements

    • Regulatory Standards

    • Company SOPs

  • Maintain audit-ready contract documentation.

  • Support inspections and quality reviews.

  • Ensure consistency and accuracy across all contract-related activities.


7. Process Improvement & Operational Excellence

  • Participate in process improvement initiatives.

  • Support departmental goals and operational efficiency projects.

  • Recommend improvements to contract workflows and tracking processes.

  • Contribute to quality and compliance enhancements.


8. Administrative & Operational Support

  • Complete assigned:

    • Training Requirements

    • Timesheets

    • Compliance Activities

  • Maintain accurate project records and reports.

  • Support overall study execution activities.


Required Skills & Competencies

Technical Skills

  • Clinical Trial Agreements (CTA)

  • Site Contract Negotiation

  • Contract Amendments

  • Budget Amendment Support

  • Clinical Research Operations

  • Site Start-Up Processes

  • Contract Lifecycle Management

  • Regulatory Documentation

  • Microsoft Office Suite

  • Contract Tracking Systems


Regulatory Knowledge

  • ICH-GCP Guidelines

  • Clinical Trial Regulations

  • Sponsor Compliance Requirements

  • Clinical Research Processes

  • Audit Readiness Standards


Soft Skills

  • Negotiation Skills

  • Communication Skills

  • Stakeholder Management

  • Attention to Detail

  • Organizational Skills

  • Time Management

  • Problem Solving

  • Multitasking Ability

  • Cross-Functional Collaboration


Educational Qualification

Minimum

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Biotechnology

    • Nursing

    • Medical Laboratory Technology

    • Allied Health Sciences

Alternative

  • Equivalent relevant clinical research experience may be considered in lieu of educational qualifications.


Potential Job Titles

  • Clinical Trial Contracts Specialist

  • Site Contracts Specialist

  • Clinical Contracts Associate

  • Study Start-Up Specialist

  • Site Activation Specialist

  • Contracts & Amendments Specialist

  • Clinical Trial Agreement (CTA) Specialist

  • Clinical Operations Contracts Specialist