Clinical Trial Project Manager

Company: Lambda Therapeutic Research

  • Location: Ahmedabad, India
  • Seniority: Senior
  • Employment type: Full-time
  • Posted: Yesterday
  • Offer language: English

Job description

Company Description Lambda Therapeutic Research is a leading full-service global Clinical Research Organization (CRO) headquartered in Ahmedabad, India, with additional operations in the USA, Canada, the UK, Spain, and Poland. The organization delivers end-to-end clinical research services to innovator, biotech, and generic pharmaceutical companies, supported by a team of over 1,200 professionals. Lambda leverages advanced technology and innovative approaches to provide a full spectrum of clinical trial solutions, including early- and late-phase trials, bioanalytical services, and pharmacovigilance. With more than two decades of experience, the company has been recognized with multiple industry awards for excellence, workplace culture, regulatory performance, and strategic partnership. Its comprehensive services span Phase 1 studies, BA/BE, data management, medical imaging, drug safety, biosimilars development, medical and scientific writing, and clinical lab services.

Role Description This is a full-time, on-site Clinical Trial Project Manager role based in Ahmedabad. The Clinical Trial Project Manager will oversee the planning, execution, and completion of clinical trials, ensuring studies are conducted in accordance with protocols, regulatory requirements, and organizational timelines. Daily responsibilities include coordinating cross-functional project teams, managing study timelines and budgets, and maintaining effective communication with sponsors and internal stakeholders. The role involves monitoring project risks and issues, preparing status reports and documentation, and supporting quality assurance activities to maintain compliance with Good Clinical Practice (GCP) and relevant regulations. The Clinical Trial Project Manager will also contribute to process improvement initiatives and mentor team members to support efficient and high-quality project delivery.

Qualifications

  • Strong project management skills, including planning, timeline management, budgeting, and risk mitigation.
  • Experience in clinical research operations, such as site management, trial coordination, and cross-functional collaboration.
  • Solid understanding of GCP, ICH guidelines, and regulatory requirements for clinical trials.
  • Proficiency in documentation, reporting, and use of clinical trial management systems or related tools.
  • Excellent communication, stakeholder management, and interpersonal skills.
  • Ability to lead and motivate teams, manage multiple projects, and make data-driven decisions.
  • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Medicine, or a related field.
  • Relevant experience in a CRO or pharmaceutical environment; prior experience as a project manager or senior clinical research professional is an advantage.
  • Strong analytical and problem-solving abilities, with attention to detail and quality.
  • Willingness to work on-site in Ahmedabad and collaborate with teams across india.

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