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Senior Project Manager

Lambda Research Accelerated
Lambda Research accelerated
15+ years
INR 15,00,000 – 25,00,000 per annum
Ahmedabad, India
10 Feb. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Job Title: Senior Project Manager – Clinical Research
Req ID: 1084
Location: Ahmedabad, Gujarat, India
Company: Lambda Therapeutic Research Ltd.
CTC Range: INR 15,00,000 – 25,00,000 per annum
Experience Required: Minimum 15 years in the pharmaceutical industry, including at least 5 years in clinical research (preferably as Project Manager – Clinical Trial Start-Up)


About the Company

Lambda Therapeutic Research Ltd. is a full-service global Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With operational facilities in Mehsana (India), Las Vegas and Pittsburgh (USA), Toronto (Canada), Warsaw (Poland), and London (UK), the organization delivers comprehensive end-to-end clinical research solutions to global innovators, biotechnology companies, and generic pharmaceutical manufacturers.

The company supports Phase I–IV clinical trials with strong regulatory, operational, and data management expertise across multiple geographies.


Role Overview

The Senior Project Manager will lead and manage global clinical trial projects from study start-up to completion. This position requires extensive pharmaceutical industry experience, deep understanding of clinical operations, regulatory processes, vendor oversight, and cross-functional team leadership within a CRO environment.

The role focuses on delivering projects on time, within budget, and in full regulatory compliance while maintaining the highest quality standards.


Key Responsibilities

  • Develop, negotiate, and manage project contracts and clinical trial budgets

  • Identify, evaluate, and select appropriate study sites

  • Coordinate with vendors for software development, validation, and system implementation

  • Prepare and review essential study documentation in accordance with regulatory guidelines

  • Ensure timely regulatory submissions and approvals

  • Optimize utilization of study resources and operational efficiency

  • Conduct and organize training programs for project teams and site staff

  • Monitor timelines, risks, and financial performance throughout the project lifecycle

  • Ensure projects are delivered in a qualitative, cost-effective, and timely manner


Required Experience

  • Minimum 15 years of experience in the pharmaceutical industry

  • At least 5 years of experience in clinical research

  • Prior experience as Project Manager in Clinical Trial Start-Up division preferred

  • Proven expertise in global clinical operations and regulatory coordination

  • Strong leadership, stakeholder management, and financial oversight capabilities


Educational Qualifications

Candidates must hold one of the following degrees from a recognized medical or life sciences background:

  • MSc (Life Sciences or related discipline)

  • M. Pharm

  • B. Pharm

  • BAMS

  • BHMS

  • BDS (Dentistry)

  • Equivalent qualification in medical sciences