Job Title: Medical Data Reviewer
Company: ICON plc
Location: Remote (India)
Job Type: Full-time
Industry: Medical & Scientific Affairs
About ICON plc: ICON plc is a world-leading healthcare intelligence and clinical research organization. With a commitment to fostering an inclusive environment driving innovation and excellence, ICON invites you to join its mission to shape the future of clinical development.
Job Description: As a Medical Data Reviewer at ICON plc, you will play a vital role in ensuring the accuracy and integrity of clinical data. Your responsibilities will include performing ongoing review of clinical/medical aspects of assigned patient data and documents, identifying errors, issuing queries for clarification, and ensuring timely follow-up. You will also conduct data trend analysis, provide project management for clinical data, and contribute to improving efficiency and quality of data deliverables.
Responsibilities:
- Perform ongoing review of clinical/medical aspects of assigned patient data and documents.
- Issue clinical data queries and ensure timely follow-up on responses from study sites.
- Conduct in-stream data trend analysis to support data quality and integrity.
- Provide project management for clinical data review activities.
- Collaborate closely with Client Clinical Scientists, Medical Directors, Data Management, and Clinical Operations.
- Participate in clinical data review meetings and data dissemination meetings.
- Contribute to the preparation and review of material for presentations and publications.
- Assist in the review and QC of clinical data sections for abstracts, manuscripts, and presentations.
- Collaborate closely with teams to ensure readiness for clinical narratives for Clinical Study Reports (CSRs).
- Contribute to the QC review of patient narratives and tracking of such.
Required Experience and Skill Set:
- Educational scientific background such as MD, PharmD, PhD, Nursing degree, MSc.
- Minimum 5 years of pharmaceutical clinical/medical data review experience, preferably 8+ years.
- Experience with Solid Tumor Oncology.
- Excellent verbal and written communication skills in English.
- Detail-oriented with strong organizational and tracking skills.
- Experience in coding review and query writing training.
- Strong clinical database navigation skills and proficiency in MS Excel.
- Proven ability to work independently and in a team setting.
- Knowledge of Good Clinical Practice and clinical trial design.
What ICON can offer you: ICON offers a competitive salary and a range of additional benefits designed to support your well-being and work-life balance. Benefits include various annual leave entitlements, health insurance offerings, retirement planning options, a Global Employee Assistance Programme, life assurance, and flexible country-specific optional benefits.
Join ICON and be part of a diverse culture that rewards high performance and nurtures talent.
