ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

What will you do:

• Serve as a Clinical Data reviewer and identify any errors in data by performing data review that require further clarification with the study site.
• Perform ongoing review of clinical/medical aspects of assigned patient data and documents (escalates to Regeneron Clinical Scientist and/or medical monitor, as appropriate)
• Examples include but not limited to: Patient eligibility, diagnosis, medical history and
• prior treatments, study drug administration, AE/SAE/AESI, con meds, safety labs,
• efficacy assessments, EOT, EOS, survival, coding, etc.
• Issues clinical data queries and ensure timely follow up following site responses as to whether the queries are appropriately addressed, and updates in EDC done, if applicable, by either closing out the queries or re-querying, as applicable
• Communicates any data training needs for CRAs, sites, etc.
• Conduct in-stream data trend analysis in support of data quality and integrity (includes protocol compliance and targeted review of patient data)
• Provide clinical data Project Management and viewed as an expert in data clinical/medical review and cleaning.
• Ensure data quality focus to audit readiness with Clinical Compliance and Systems Validation Compliance.
• May assist in review and contribute to data capture requirements guidance in line with protocol and reporting requirements.
• Monitor site data entry performance and provide leadership to identify root causes of data issues and implement remedial actions.
• Ensure timely follow-up and resolution of data related compliance issues.
• Continuously assess opportunities to improve efficiency of tasks and quality of data deliverables. May contribute to EDC completion training.
• May participate in clinical data review meetings such as:
• Protocol Deviation review
• Data Review and Quality Team (DRQT)
• Statistical Review of Clinical Data (SRCD)
• Safety Monitoring Team (SMT) review
• Slide preparation of top-line results
• May be involved in preparing or review material for and presents in data dissemination meetings, such as:
• Investigator meetings, advisory boards, safety cohort review meetings, IDMC, SC, senior management meetings, central imaging review, CST/SPT/DPR/PRC discussions for study/program decisions
• May be involved in review and QC clinical data sections for abstracts / manuscripts/ oral and poster presentations
• Will collaborate closely with Regeneron Clinical Scientists, Medical Directors, Data Management and Clinical Operations to execute clinical data reviews and activities prior to data cuts for snapshots, interim analysis, DSUR, IBs, regulatory requests, study site close-outs and final DBL.
• May be closely involved in data review and identification of readiness for clinical narratives for Clinical Study Report (CSR)
• May be involved in QC review of patient narratives and contribute to tracking of such.

Your Profile:

• Educational scientific background such as MD, PharmD, PhD, Nursing degree, MSc
• ≥ 5 years of pharmaceutical clinical/medical data review experience is required, including clinical crosscheck experience. 8+ years is preferrable.
• Experience with Solid Tumor Oncology
• Excellent verbal and writing communication in English, organization and tracking skills. Strong operational skills and demonstrated ability to meet timelines.
• Detail oriented
• Experience in coding review
• Query writing training
• Strong clinical database navigation skills
• Strong MS excel, project management
• Proven ability to work independently and in a team setting.
• Knowledge of Good Clinical Practice; comprehensive knowledge of clinical trial design; understanding of the overall drug development process

Required qualifications and experience:

• Medical degree or advanced healthcare qualification (e.g., MD, MBBS, PharmD, or equivalent), or a life sciences degree with relevant clinical experience.
• Experience in clinical research, pharmacovigilance, or medical monitoring, preferably within a CRO, pharma, or related environment.
• Strong understanding of clinical trial design, GCP, safety reporting, and medical terminology.
• Excellent analytical skills and attention to detail, with the ability to interpret complex clinical data.
• Good communication and collaboration skills, with the ability to work effectively in cross-functional, global teams.
• Comfort working with electronic data capture systems, listings, and standard data formats.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply