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Fsp Site Contract Specialist – Remote Clinical Research

Propharma
Propharma
5+ years
Not Disclosed
Remote, USA, Remote
1 May 7, 2026
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing

FSP Site Contract Specialist – Remote Clinical Research Contract Specialist Job in USA

Company: ProPharma
Job Title: FSP Site Contract Specialist
Location: United States
Job Type: Full-Time
Work Mode: Remote / Hybrid
Department: Global Clinical Study Support
Job ID: JR 9604


About ProPharma

ProPharma is a leading global life sciences consulting organization supporting pharmaceutical, biotechnology, and medical device companies throughout the product lifecycle. With expertise in clinical research, regulatory affairs, pharmacovigilance, quality compliance, and medical information, ProPharma helps accelerate drug development and improve patient outcomes worldwide.


Job Overview

ProPharma is seeking an experienced FSP Site Contract Specialist to support global clinical trial study start-up and site contract management activities. The role focuses on negotiating, managing, and executing clinical trial agreements and related contractual documents for clinical research studies.

The selected candidate will collaborate closely with:

  • Clinical Operations Teams
  • Investigators and Research Sites
  • CRO Partners
  • Study Start-Up Teams
  • Sponsors and Global Negotiation Networks

This opportunity is ideal for professionals experienced in:

  • Clinical Trial Agreements (CTAs)
  • Site Contract Negotiation
  • Study Start-Up
  • Budget Negotiations
  • CRO Operations
  • Clinical Research Administration

Experience Required

Required Experience

  • Minimum 5 years of experience in:
    • Clinical Research
    • Site Contracts
    • Study Start-Up
    • Clinical Trial Administration
    • CRO or Pharmaceutical Industry Operations

Preferred Industry Background

Candidates should have experience working with:

  • Pharmaceutical Companies
  • Biotechnology Organizations
  • CROs (Contract Research Organizations)
  • Clinical Research Support Organizations

Freshers Eligibility

  • Freshers are not eligible
  • This is an experienced-level clinical contracts and study start-up role

Educational Qualification

Candidates should possess:

  • Bachelor’s degree in:
    • Business
    • Life Sciences
    • Healthcare
    • Nursing
    • Related scientific or healthcare disciplines

Equivalent experience may also be considered.


Key Responsibilities

Clinical Trial Contract Management

  • Develop and manage:
    • Confidential Disclosure Agreements (CDAs)
    • Clinical Trial Agreements (CTAs)
    • Other clinical research contractual documents
  • Support contract drafting, review, negotiation, and execution

Contract Negotiation

  • Negotiate contractual terms with:
    • Investigator sites
    • Sponsors
    • Clinical research partners
  • Follow escalation and negotiation procedures
  • Ensure timely contract completion and approvals