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IQVIA Hiring Contracts Specialist – Clinical Operations

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Location: Thฤne, Mahฤrฤshtra, India
Job Type: Full-Time
End Date: April 23, 2025
Industry: Pharmaceutical / Clinical Research
Company: IQVIA

About IQVIA

IQVIA is a global leader in clinical research, healthcare analytics, and commercial solutions for the life sciences industry. With a focus on accelerating medical advancements, IQVIA provides intelligent insights to improve patient outcomes worldwide.

If you are looking for pharma jobs in Thฤne or clinical research jobs in India, this Contracts Specialist 1 role could be the perfect opportunity for you.

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Job Overview: Contracts Specialist 1 – Clinical Operations

As a Contracts Specialist 1 at IQVIA, you will support start-up contracting activities for clinical trials, ensuring compliance with regulatory and sponsor requirements. This role involves budget estimation, contract negotiations, and document management to facilitate smooth clinical trial operations.

Key Responsibilities

  • Develop investigator grant estimates and proposal text for clinical trials.
  • Maintain contract and budget templates, ensuring compliance with project plans.
  • Collaborate with sponsors, stakeholders, and regional teams to meet contracting timelines.
  • Provide financial and operational contracting support for business development.
  • Review and prepare scientific, technical, and administrative documentation.
  • Track and report contracting performance metrics and out-of-scope activities.
  • Ensure contract compliance with GCP/ICH guidelines and regulatory standards.
  • Maintain accurate records in CTMS (Clinical Trial Management System) and other tracking tools.

Qualifications & Skills Required

Education & Experience

  • Bachelorโ€™s Degree (Required)
  • 1+ years of experience in contract negotiation or clinical research.
  • Experience in clinical trial contract management is preferred.

Essential Skills

  • Strong negotiation and communication skills.
  • Excellent technical writing abilities.
  • Knowledge of GCP/ICH guidelines and regulatory requirements.
  • Proficiency in Microsoft Office (Excel, Word, Outlook).
  • Ability to work in a matrix team environment.
  • Strong organizational and planning skills.
  • Understanding of clinical trial budgeting and pricing models.

Why Join IQVIA?

  • Work with a global leader in clinical research and healthcare intelligence.
  • Opportunity to contribute to life-changing medical advancements.
  • Collaborative and growth-oriented work environment.
  • Competitive salary and career development opportunities.

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