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Clinical Contract Associate I

Abbott
Abbott
2-3 years
Not Disclosed
Gurgaon, India
10 April 14, 2026
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science 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

Clinical Contract Associate I – Gurgaon | Clinical Contracts & Budgets | Pharma Jobs

Company: Global Medical Device / Clinical Research Organization
Location: Gurgaon
Job Type: Full-Time
Work Mode: On-site / Hybrid
Experience: 2–3 Years
Qualification: Bachelor’s Degree (Life Sciences / Finance / Business / Related Field)


Job Overview

This role sits at the core of clinical trial financial and contractual operations. As a Clinical Contract Associate I, you will support global clinical studies by managing site budgets, HCP agreements, and contract amendments.

You will work closely with US & CALA teams, gaining international exposure in clinical contracts, budget development, and regulatory-compliant agreement management—making it a strong career path in clinical operations and pharma finance.


Key Responsibilities

Clinical Budget Management

  • Develop and update site budget templates for multi-country clinical studies
  • Support protocol amendments by updating budget structures and cost elements
  • Maintain budget comparison files for study forecasting and financial tracking

Clinical Contracts & Agreements

  • Support licensing agreements for clinical trial tools and outcome assessments
  • Manage HCP (Healthcare Professional) agreements, including documentation and approvals
  • Perform FMV (Fair Market Value) assessments and route agreements for signatures

Amendments & Documentation

  • Handle routine contract amendments (e.g., PI change, site updates)
  • Maintain accurate documentation in systems like GPAS
  • Ensure compliance with contractual and regulatory standards

Cross-functional Collaboration

  • Work with Site Operations and Project Management teams for financial planning
  • Support global teams (US & CALA regions) for contract and budget activities
  • Contribute to process improvement initiatives in clinical contract operations

Required Skills & Qualifications

Educational Requirements

  • Bachelor’s degree in:
    • Life Sciences
    • Finance / Accounting
    • Business Administration
    • Related discipline

Experience

  • 2–3 years of experience in Clinical Research / Contracts / Budgets
  • Experience in pharma, CRO, or medical device industry preferred

Core Skills & Technical Expertise

  • Strong knowledge of clinical trial budgeting and contract management
  • Understanding of HCP agreements and regulatory compliance
  • Experience with financial analysis, forecasting, and Excel-based reporting
  • Familiarity with clinical research processes and SOPs
  • Exposure to FMV assessments and licensing agreements

Preferred Skills

  • Experience in contract negotiation and budget development
  • Exposure to global clinical trials and multi-country studies

Soft Skills

  • Strong analytical and problem-solving skills
  • High attention to detail and accuracy
  • Ability to manage multiple stakeholders and deadlines
  • Excellent communication and coordination skills

Perks & Benefits

  • Exposure to global clinical contract and budget operations
  • Career growth in clinical finance, contracts, and regulatory domains
  • Opportunity to work with international teams (US & CALA regions)
  • Structured learning and professional development
  • Collaborative and process-driven work environment

About the Company

This organization is a global leader in clinical research and medical device innovation, supporting pharmaceutical and biotech companies in managing clinical trials, regulatory compliance, and financial operations. It plays a key role in advancing healthcare through efficient and compliant clinical study execution.


Salary / Compensation

💰 Not disclosed (Competitive industry-standard package)


Work Mode

📍 On-site / Hybrid – Gurgaon, India


Call to Action

If you want to build expertise in clinical contracts, budgeting, and global trial operations, this role offers a strong and scalable career path.

👉 Apply now and grow your career in clinical research contracts and pharma operations.