Parexel is hiring for two clinical research and pharmaceutical industry roles in India: Supply & Logistics Specialist and Study Grant Analyst II. Both positions are listed for Hyderabad, India – Remote and are suited to professionals with experience in clinical research, pharmaceuticals, clinical operations, study budgets, logistics, or related healthcare functions.

1. Supply & Logistics Specialist – Parexel

Job Title: Supply & Logistics Specialist / Senior Supply & Logistics Specialist
Job ID: R0000041875
Location: Hyderabad, India – Remote
Job Type: Full Time
Application Deadline: September 30, 2026

About the Role

The Supply & Logistics Specialist (SLS/SrSLS) supports the Supply & Logistics Project Manager in developing and executing clinical trial supply chain strategies.

The role involves clinical trial supply and logistics, sourcing, distribution, inventory planning, third-party provider management, project coordination and GxP compliance.

The specialist will help ensure that clinical trial supply activities are delivered on time, within budget and according to applicable quality and regulatory requirements.

Key Responsibilities

• Support the Supply & Logistics Project Manager in developing study-specific logistics strategies.
• Develop clinical supply, sourcing and distribution strategies.
• Monitor project scope, timelines, budgets and risks.
• Maintain study-specific management tools and documentation.
• Support resource planning for Clinical Trial Supply & Logistics activities.
• Manage pass-through costs and reporting.
• Coordinate with third-party logistics providers and procurement teams.
• Help negotiate provider scope of work.
• Develop inventory plans based on forecasts and study requirements.
• Prepare and maintain supply schedules.
• Coordinate with clinical teams regarding study progress.
• Provide feedback to depots and relevant stakeholders.
• Identify opportunities for process improvement.
• For senior-level responsibilities, mentor Clinical Supply Specialists and Clinical Supply Assistants.
• Ensure activities comply with ICH GCP and GxP requirements.

Skills Required

Candidates should demonstrate:

• Clinical logistics or pharmaceutical industry knowledge.
• Project management capabilities.
• Strong communication and stakeholder-management skills.
• Negotiation and customer-management skills.
• Ability to manage multiple projects and priorities.
• Strong attention to detail.
• MS Office proficiency.
• Ability to work effectively in a matrix environment.
• Understanding of GxP regulatory requirements.
• Problem-solving and creative solution development.
• Strong written and verbal English communication.

Education

Parexel states that candidates should have a B.A./B.S. or Master’s degree, or equivalent qualification such as Pharm.D., in biology, pharmacy or another health-related discipline, international trade, business administration, logistics, or a relevant field/work experience.

Experience

The position calls for extensive pharmaceutical, clinical research or consulting experience, with strong experience in clinical logistics or a related biopharmaceutical field, project management and cross-functional activities.

2. Study Grant Analyst II – Parexel

Job Title: Study Grant Analyst II
Job ID: R0000045672
Location: Hyderabad, India – Remote
Job Type: Full Time
Posted: September 21, 2026

About the Role

The Study Grant Analyst II will support the preparation, analysis and management of clinical study grants and investigator site budgets for Phase I–IV clinical trials.

The position involves clinical study pricing, Fair Market Value (FMV) assessment, budget development, client proposals, post-award analysis and collaboration with Site Contracts Leaders, Study Project Leaders and Project Directors.

Key Responsibilities

• Prepare accurate and competitive clinical study grants.
• Work with clinical study pricing tools such as GrantPlan.
• Support budget development for pre-sales proposals.
• Ensure clinical study grants comply with RFP requirements and internal policies.
• Lead or support creation, revision, escalation and approval of clinical study grants.
• Conduct post-award clinical study grant analyses.
• Participate in budget reviews and strategy sessions.
• Support competitor benchmarking and client-needs analysis.
• Apply Fair Market Value principles.
• Maintain awareness of healthcare compliance requirements.
• Understand relevant requirements including HIPAA, FCPA and Safe Harbor.
• Share lessons learned and knowledge with the team.
• Support grants analysis and performance monitoring.
• Contribute to departmental training and process improvement.
• Maintain compliance with ICH Guidelines, GCP and regulatory requirements.
• Participate in system and process improvement initiatives.

Skills Required

Candidates should have:

• Strong strategic thinking skills.
• Excellent analytical and problem-solving abilities.
• Strong communication skills.
• Client and stakeholder-management experience.
• Negotiation and influencing capabilities.
• Strong organizational skills.
• Advanced Microsoft Excel, PowerPoint and Word skills.
• Familiarity with clinical research/eClinical systems.
• Ability to manage multiple projects simultaneously.
• Ability to work independently while knowing when to escalate issues.
• Strong understanding of business and customer implications.
• Ability to work effectively in a virtual team environment.

Experience Required

Parexel specifies 3–5 years of experience in clinical site budget development, including experience using tools such as GrantPlan or Grant Manager, preferably within managed care, pharmaceutical or biotechnology organizations.

Experience with industry benchmarking databases and tools used to determine Fair Market Value for investigator grants is also required.

Education

A degree in biological science, pharmacy or another health-related discipline is preferred. Equivalent nursing or relevant clinical experience may also be considered.

Who Can Apply?

Supply & Logistics Specialist

Relevant backgrounds include:

• Pharm.D
• B.Pharm
• M.Pharm
• B.Sc./M.Sc. Biology or Life Sciences
• Health-related disciplines
• Business Administration
• Logistics
• International Trade
• Relevant clinical research or pharmaceutical experience

Candidates should particularly have experience in clinical supply, clinical logistics, pharmaceutical operations or biopharmaceutical project management.

Study Grant Analyst II

Relevant candidates may come from:

• Pharmacy
• Pharm.D
• Biological Sciences
• Life Sciences
• Nursing
• Other health-related disciplines

However, education alone is not sufficient for the Study Grant Analyst II position. The job specifically asks for 3–5 years of clinical site budget development experience, including relevant grant/budgeting tools and FMV benchmarking experience.

Benefits & Career Opportunities

The supplied job descriptions do not specify a detailed employee-benefits package. However, these positions offer exposure to areas such as:

• Clinical research operations
• Clinical trial supply chain
• Pharmaceutical logistics
• Clinical study budgeting
• Investigator grants
• Fair Market Value analysis
• GxP and GCP compliance
• Cross-functional project management
• Global stakeholder management
• Biopharmaceutical operations

How to Apply

Application Link For Supply & Logistics Specialist:

Application Link For Study Grant Analyst II: