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Bristol Myers Squibb is Hiring for Site Contract Specialist | Clinical Research

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If you are looking to build a career in clinical research and pharmaceutical operations, this opportunity with Bristol Myers Squibb offers an excellent pathway. The role of Site Contract Specialist is designed for professionals who want to contribute to clinical trials and make a real impact on patient lives.

Located in Hyderabad, this position provides exposure to global clinical operations while working with high-performing teams in a structured and growth-oriented environment.


About the Company

Bristol Myers Squibb is a globally recognized biopharmaceutical company focused on transforming patientsโ€™ lives through science. The company works across areas like oncology, hematology, immunology, and cardiovascular diseases, offering innovative treatments and therapies.

Employees at BMS benefit from a collaborative culture, career growth opportunities, and a strong emphasis on work-life balance.


Job Overview

Position: Site Contract Specialist
Location: Hyderabad, Telangana, India
Industry: Pharmaceutical / Clinical Research

The Site Contract Specialist plays a key role in clinical trial execution by managing contracts and budgets with research sites. This role ensures that studies start on time and operate efficiently.


Roles and Responsibilities

As a Site Contract Specialist, you will:

  • Prepare, review, negotiate, and finalize clinical site contracts
  • Manage investigator budgets using standard templates
  • Coordinate with internal teams and external research sites
  • Ensure accuracy and compliance of contract documentation
  • Handle routine contract-related queries and escalate complex issues
  • Track operational metrics like cycle time and quality
  • Identify process improvements and efficiency opportunities
  • Collaborate with legal, finance, and clinical operations teams

Required Qualifications

To be eligible for this role, candidates should have:

  • Bachelorโ€™s degree in Life Sciences, Business Administration, or related field
  • Experience in clinical trial contracting or clinical operations
  • Strong attention to detail and multitasking ability
  • Excellent communication skills (written & verbal)
  • Ability to work in a regulated and process-driven environment
  • Familiarity with contract management tools and business software

Preferred Qualifications

  • Experience in clinical studies
  • Knowledge of investigator grants and budget negotiations
  • Experience with electronic contract/document management systems

Salary and Benefits

Estimated Salary Range: โ‚น6,00,000 โ€“ โ‚น12,00,000 per annum (based on experience)

Benefits include:

  • Competitive compensation package
  • Health and wellness programs
  • Work-life balance and flexible environment
  • Career growth and learning opportunities
  • Exposure to global clinical projects

Application Link

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