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Technical Officer (Report Writing) at Lambda Therapeutic Research

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Looking to advance your career in clinical research report writing? Lambda Therapeutic Research Ltd. is hiring a Technical Officer โ€“ Report Writing in Ahmedabad. This is an excellent opportunity for candidates with M.Pharm (Pharmacology) or Pharm.D and experience in Clinical Study Report (CSR) writing, especially in early-phase (BABE) studies.

With over 20 years of CRO expertise and global operations, Lambda Therapeutic Research offers strong exposure to regulatory medical writing, ICH E3 guidelines, and clinical documentation standards, making this role ideal for professionals aiming to grow in clinical research and medical writing careers in India.


Key Responsibilities โ€“ Report Writing Role

  • Prepare and review Clinical Study Reports (CSRs) for BABE (early-phase) studies
  • Ensure compliance with ICH E3 regulatory guidelines
  • Collaborate with project teams, QA, and regulatory teams
  • Maintain high-quality standards in medical and regulatory writing
  • Contribute to process improvement, training, and resource management
  • Support cross-functional coordination for timely report delivery

Eligibility Criteria & Qualifications

  • Educational Qualification:
    • M.Pharm (Pharmacology) OR Pharm.D
  • Experience Required:
    • 1โ€“4 years in clinical report writing / medical writing
    • Experience in CSR writing for clinical trials preferred
  • Key Skills:
    • Knowledge of ICH E3 guidelines
    • Understanding of regulatory expectations in medical writing
    • Strong analytical and documentation skills
    • Team collaboration and communication

Salary & Benefits

  • CTC Range: โ‚น3.5 LPA โ€“ โ‚น6 LPA
  • Opportunity to work with a global CRO
  • Exposure to international regulatory standards
  • Career growth in clinical research and medical writing domain
  • Collaborative and learning-driven work environment

Why Choose Lambda Therapeutic Research?

  • Established global clinical research organization (CRO)
  • Presence across India, USA, UK, and Europe
  • Strong pipeline of clinical trials and regulatory projects
  • Focus on innovation, compliance, and quality delivery

Job Location

  • Ahmedabad, Gujarat, India

How to Apply

Application Link

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