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0-2 years
Not Disclosed
Bangalore, India
8 June 2, 2026
Job Description
Job Type: Full Time Hybrid Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Apache Spark, Artificial Intelligence (AI), Big Data, Data Governance, Data Literacy, Data Management, Data Quality, Data Science, Data Strategies, Data Visualization, Machine Learning (ML), Master Da, Auditing, Audit Management, Audits Compliance, Communication, Continued Learning, Decision Making, Gmp Procedures, Inspection Readiness, Managing Ambiguity, Organizing, People Management and Leadershi, Bachelor’s Degree (BS) or Master’s Degree (MS) in: Life Sciences Pharmacy Biotechnology Biomedical Sciences Chemistry Regulatory Affairs Or related scientific disciplines, Budget Management, Clinical Trials, Negotiation Skills, Process Improvement, Project Planning, Vendor Management, Waterfall Model, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Intern, Causality Assessment, Change Control, Continual Improvement Process, Data Analytics and Digital, GDP Knowledge, gmp knowledge, HSE Knowledge, Manufacturing Process, Manufacturing Production, Operational Excellence, Process, Clinical Monitoring, Clinical Research, Clinical Study Reports, Clinical Trial Management Systems, Clinical Trials, Collaboration, Data Integrity, Decision Making Skills, Lifesciences, Clinical Research, Clinical Trials, Curious Mindset, Databases, Drug Development, Job Description, Lifesciences, Medical Communication, Medical Information, Medical Writing, Military Intelligence, Pat, Clinical SAS Programming, Clinical Trials, Cross-Functional Teams, Drug Development, Lifesciences, Negotiation Skills, People Management, Problem Solving Skills, Regulatory Compliance, Risk Management, Strategy Execution, Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Clinical Trials, Functional Teams, Literature Review, Management Skills, Medical Information, Medical Records, Medical Strategy, Pharmacovigilance, Regulatory Compliance, Risk Management, Safety Scien, Coaching Skills, Data Science, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Pro, Collaboration, Communication Skills, gmp, GMP Guidelines, Operational Excellence, Problem Solving Skills, Quality Agreements, Quality Compliance, Quality Management, Quality Standards, Regulatory Requ, Communication Skills, Continual Improvement Process, Master Data, Material Requirements Planning (Mrp), Materials Management, People Management, Production Planning, Supplier Relationship Management (Srm), Supply-Chain Man, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Resource Analyst

Company: Thermo Fisher Scientific (PPD Clinical Research Portfolio)
Work Schedule: Standard (Monday–Friday)
Work Environment: Office (Clinical/Office setting)
Location: Not specified (likely hybrid/onsite depending on assignment)


About the Company

Thermo Fisher Scientific is a global leader in scientific research and clinical development, supporting pharmaceutical and biotech companies worldwide. Through its clinical research services (PPD portfolio), the company contributes to the development of life-changing therapies across 100+ countries.


Role Overview

The Resource Analyst is responsible for workforce planning and resource allocation across clinical projects. The role focuses on forecasting, tracking, and optimizing utilization of clinical resources to ensure efficient project execution, client satisfaction, and operational profitability.


Key Responsibilities

1. Resource Planning & Allocation

  • Track and identify resource requirements for projects

  • Assign staff based on:

    • Client requirements

    • Therapeutic area expertise

    • Geographic location

    • Availability and experience

  • Recommend appropriate team composition for projects

2. Resource Coordination

  • Manage intake and resolution of resource requests

  • Maintain project and resource tracking systems

  • Update assignments and roll-off dates for clinical resources

  • Distribute and coordinate CVs with internal teams

3. Reporting & Analysis

  • Use resourcing dashboards for tracking utilization and forecasting

  • Reconcile and quality-check departmental reports

  • Support monthly reporting on:

    • Resource utilization

    • Forecasting projections

  • Prepare and distribute resource reports to leadership

4. Stakeholder Management

  • Coordinate weekly resourcing meetings

  • Engage with senior stakeholders (Associate Director, Director, Senior Director, Executive Director)

  • Collaborate with internal departments for RFPs and bid defense planning

5. Operational Support

  • Ensure CVs are up to date in coordination with CV administrator teams

  • Support special projects as required

  • Liaise across teams to prioritize resourcing for upcoming work


Required Qualifications

  • Bachelor’s degree or equivalent qualification

  • 0–2 years of relevant experience (or equivalent combination of education and experience)


Key Skills Required

Technical & Analytical Skills

  • MS Office proficiency (Excel, Outlook)

  • Strong analytical and quantitative ability

  • Ability to work with dashboards and reporting tools

Core Competencies

  • Strong problem-solving skills

  • Attention to detail

  • Ability to multitask and manage multiple priorities

  • Good data interpretation skills

Communication Skills

  • Strong verbal and written communication

  • Ability to interact with senior leadership and cross-functional teams


Work Environment

  • Office-based role (clinical or corporate environment)

  • Exposure to standard office equipment

  • Occasional travel or site visits may be required


What Makes This Role Important

  • Ensures optimal utilization of clinical research staff

  • Supports global clinical trials and pharmaceutical research operations

  • Directly impacts project efficiency, cost control, and delivery timelines

  • Contributes to healthcare innovation and drug development