Job Title: Senior Project Manager
Job Category: Clinical Project Management / Pharmaceutical Research / Clinical Trials
Job Type: Full-Time
Experience Level: 15+ Years (Minimum 5 years in Clinical Research Project Management)
Location: Ahmedabad, Gujarat, India
Req ID: 1084
CTC Range: INR 15,00,000 – 25,00,000 per annum
Company Overview
Lambda Therapeutic Research Ltd. is a global full-service Clinical Research Organization (CRO) headquartered in Ahmedabad, India. With operations across India, North America, and Europe, Lambda delivers end-to-end clinical research services to innovator, biotech, and generic pharmaceutical companies worldwide.
The organization specializes in providing comprehensive support for clinical trials, regulatory compliance, and drug development programs, ensuring timely, high-quality, and cost-effective outcomes for global clients.
Role Overview
Lambda Therapeutic Research is seeking a Senior Project Manager to lead complex clinical research projects. The role involves planning, executing, and monitoring clinical trials while managing cross-functional teams, budgets, and regulatory submissions. The ideal candidate will have extensive experience in the pharmaceutical industry, with proven leadership in clinical trial project management.
Key Responsibilities
Develop project contracts, budgets, and timelines to ensure efficient resource utilization.
Identify, select, and manage study sites, ensuring alignment with project objectives.
Collaborate with vendors to develop, validate, and implement study-related software solutions.
Prepare study protocols, regulatory documents, and operational plans.
Ensure timely submissions to regulatory authorities and obtain necessary approvals.
Conduct training sessions for study teams and site staff to maintain high compliance standards.
Monitor project progress, resolving issues to ensure projects are delivered on time, within scope, and budget.
Maintain high-quality standards while optimizing cost and resource efficiency.
Required Experience
Minimum 15 years of experience in the pharmaceutical industry.
At least 5 years of hands-on experience in clinical research project management, preferably within startup clinical trial divisions.
Proven expertise in managing multi-site clinical trials, budgets, and regulatory compliance.
Educational Qualification
MSc, M. Pharm, B. Pharm, BAMS, BHMS, BDS, or equivalent degree in medical or pharmaceutical sciences.
This opportunity is ideal for senior professionals with extensive clinical trial management experience looking to lead global projects in a dynamic and growth-focused CRO environment.
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