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Senior Project Manager

5-15 years
₹15,00,000 – ₹25,00,000 per annum
10 Nov. 11, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, 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, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Project Manager

Company: Lambda Therapeutic Research Ltd.
Req ID: 1084
Location: Ahmedabad, India
Date Posted: 10 Nov 2025
CTC Range: ₹15,00,000 – ₹25,00,000 per annum


Company Overview

Lambda Therapeutic Research is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With operations in:

  • Mehsana (India)

  • Las Vegas (USA)

  • Pittsburgh (USA)

  • Toronto (Canada)

  • Warsaw (Poland)

  • London (UK)

Lambda provides end-to-end clinical research solutions to innovator, biotech, and generic pharmaceutical companies worldwide.


Job Summary

The Senior Project Manager is responsible for leading and overseeing clinical trial projects from startup to completion. This includes contract development, site selection, regulatory coordination, resource planning, and ensuring projects are executed within timelines, quality requirements, and budget.


Key Responsibilities

1. Project Setup & Planning

  • Develop project contracts and budgets.

  • Identify, evaluate, and select appropriate clinical study sites.

  • Coordinate with vendors to develop, validate, and deploy software/tools required for studies.

2. Documentation & Regulatory Activities

  • Prepare all study-related documentation, including protocols, plans, and manuals.

  • Ensure timely regulatory submissions, approvals, and compliance with global and local guidelines.

3. Study Execution & Oversight

  • Efficiently manage and allocate study resources across all study phases.

  • Conduct and organize training sessions for study teams and site personnel.

  • Oversee project progress to ensure cost-effective, high-quality, and timely delivery.

4. Leadership & Coordination

  • Provide strategic guidance to project teams.

  • Ensure clear communication between cross-functional teams, vendors, and study sites.

  • Drive problem-solving, risk management, and decision-making for project success.


Experience Required

  • Minimum 15 years of experience in the pharmaceutical industry.

  • At least 5 years of experience in clinical research.

  • Preferably experience as a Project Manager in Clinical Trials – Startup Division.


Educational Qualifications

  • M.Sc., M.Pharm, B.Pharm, BAMS, BHMS, BDS, or equivalent degree in medical/clinical sciences.