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Date Posted
12-Jul-2026
Location
Delhi (DL), 1
Job Type
Full Time
Company
Huntsman
Description
Job Title: Clinical Study Grant Manager (Remote)
Job ID: R0000032977
Location: India, Remote
Additional Locations: India-Bengaluru-Remote
Category: Administrative
About This Role:
As a Clinical Study Grant Manager, you will play a critical role in the preparation and management of clinical study grants (Phases I – IV) for various clinical indications. You will be responsible for ensuring timely and accurate creation of competitive clinical study budgets, collaborating with the proposal team, and ensuring compliance with internal and external regulations.
Key Responsibilities:
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Grant Preparation:
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Prepare accurate and competitive Clinical Study grants using Clinical Study Pricing Tools (e.g., Grants Manager).
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Collaborate with the Proposal team to create budget concepts for Pre-sales business proposals, ensuring compliance with RFPs and internal policies.
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Lead on Clinical Study Grants:
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Serve as the Subject Matter Expert (SME) in the creation, revision, escalation, and approval process for Clinical Study grants.
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Work with the Site Contracts Leader, Study Project Leader, and Project Director to ensure grant preparation and approval for awarded projects.
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Conduct additional post-award clinical study grant analysis.
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Strategy and Budget Reviews:
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Participate in strategy sessions and budget reviews to develop win themes, assess competitors, and discuss client needs.
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Ensure compliance with Fair Market Value (FMV) principles and the Physician Payments Sunshine Act.
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Healthcare Compliance:
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Stay informed about healthcare compliance guidelines (HIPAA, FCPA, Safe Harbor, etc.) and ensure that all grant-related activities comply with them.
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Team Collaboration and Knowledge Sharing:
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Share lessons learned and new scenarios with the team to enhance collective knowledge and performance.
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Help develop and deliver departmental or functional training plans.
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General Administration & Operations:
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Ensure compliance with applicable ICH Guidelines, Good Clinical Practices, Regulatory Agency requirements, and PAREXEL SOPs.
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Participate in Parexel and departmental system/standards improvement activities.
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Maintain agreed productivity/billability levels and complete routine administrative tasks (e.g., timesheets, travel expense claims).
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Maintain a positive work environment, fostering teamwork and open communication.
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Implement process improvements based on client and team feedback.
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Skills and Competencies:
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Strategic Thinking: Ability to create urgency and proactively resolve issues in complex situations.
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Analytical and Problem-Solving Skills: Strong ability to define and resolve issues in various scenarios.
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Client-Focused: Ability to build and maintain trust with clients, becoming involved in the client’s decision-making process.
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Communication Skills: Strong communication abilities across functional lines, both internally and externally.
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Negotiation and Influencing: Outstanding skills in negotiation, influencing, and stakeholder management.
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Organizational Skills: Ability to manage a full workload across multiple projects, prioritize effectively, and maintain attention to detail.
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Proficiency: Proficient in Microsoft Excel, PowerPoint, Word, and industry-standard eClinical systems.
Knowledge and Experience:
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Experience:
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3-5 years of experience in clinical site budget development, with expertise in tools like Grant Plan or Grant Manager, in the pharmaceutical or biotechnology industries.
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Familiarity with industry benchmarking databases and tools for ensuring fair market value in the development of investigator grants.
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Education:
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A degree in biological sciences, pharmacy, or another health-related discipline.
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Additional Information:
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Work Environment: Remote, with the possibility of travel as needed.
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#LI-REMOTE: This is a remote position.
This structured format makes the role and responsibilities clear and easily digestible. Let me know if you need any additional adjustments!
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