PHARMAFull-time
Study Grant Analyst II
HYDERABAD (India)REMOTEPOSTED: 9/21/2026
PHARMAFull-time
HIRING ORGANIZATIONPAREXELBiosciences / Healthcare, Contract Research Organization (CRO)
ROLE OVERVIEW
Study Grant Analyst II responsible for developing and analyzing clinical study grants for Phase I-IV trials, supporting pre-sales proposals and awarded projects, and ensuring compliance with fair market value and healthcare regulations.
ROLE DEFINITION & RESPONSIBILITIES
- •Prepare accurate clinical study grant estimates for Phase I-IV studies
- •develop budget concepts for pre-sales proposals in line with RFP requirements and internal policies
- •lead grant creation, revision, escalation, and approval activities for awarded projects
- •conduct post-award grant analyses and support budget reviews
- •ensure compliance with FMV principles, Physician Payments Sunshine Act, HIPAA, FCPA, Safe Harbor, ICH/GCP, and SOP requirements
- •provide grant analysis, knowledge sharing, and training support
- •contribute to system, standards, quality, and process improvement initiatives
Reporting Hierarchy: Reports within Parexel Clinical Research Services and works closely with Site Contracts Leaders, Study Project Leaders, Project Directors, Proposal teams, clients, and senior management.
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- 3-5 years of experience in clinical site budget development
- experience using GrantPlan, Grant Manager, or similar tools
- experience in pharmaceutical, biotechnology, managed care, or clinical research environments
- experience with industry benchmarking and FMV tools
- strong analytical and problem-solving skills
- proficiency in Microsoft Excel, PowerPoint, and Word
- stakeholder and client relationship management experience
PREFERRED QUALIFICATIONS
- •Degree in biological science, pharmacy, or another health-related discipline
- •equivalent nursing qualification or relevant clinical experience
- •familiarity with healthcare compliance requirements
- •experience with standard business and eClinical systems
- •negotiation and influencing skills
REQUIRED VERIFIED SKILLS
Clinical study budgeting
GrantPlan
Grant Manager
clinical research
FMV analysis
analytical problem-solving
stakeholder management
client communication
Microsoft Excel
PowerPoint
Word
ICH/GCP compliance
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Standard Parexel employee benefits; professional development and training opportunities; remote work arrangement
Salary is not stated in the provided posting; no salary figures are inferred.
ORGANIZATION CONTEXT & CULTURE
Parexel is a global clinical research and biopharmaceutical services organization providing clinical development, regulatory, consulting, and market access solutions.
TEAM SIZE: Large global organization
INDUSTRY: Biosciences / Healthcare, Contract Research Organization (CRO)
Culture: Client-focused, collaborative, results-oriented, quality-driven, and designed for effective virtual teamwork.
EXPECTED CAREER ROADMAP
Opportunity to deepen expertise in clinical site budgeting, grants management, FMV analysis, clinical research operations, client consulting, and proposal support.
APPLICATION ADVISORY
Highlight 3-5 years of clinical site budget experience, GrantPlan/Grant Manager expertise, FMV and benchmarking knowledge, and experience with pharmaceutical or biotechnology clients. Emphasize Excel proficiency, analytical skills, compliance knowledge, and stakeholder management.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.