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About the Role
IQVIA has several exciting freelance CRA positions available in the UK, requiring travel across the country for site visits.
Responsibilities
- Participate in the preparation and execution of Phase I-IV clinical trials.
- Oversee clinical investigation progress through site evaluation, initiation, and interim close-out visits.
- Monitor clinical trials in accordance with Good Clinical Practices and IQVIA Biotech procedures.
- Collaborate with the Clinical Trial Manager (CTM) and/or Lead CRA to ensure monitoring activities meet study requirements.
- Participate in the investigator recruitment process, performing site evaluation visits.
- Coordinate site and internal department activities for study initiation.
- Perform study initiation activities, including protocol review, regulatory issue discussion, and training on eCRF and EDC systems.
- Assist in resolving issues to ensure compliance with site file audits.
- Ensure adherence to Good Clinical Practices, investigator integrity, and study procedures through on-site monitoring.
- Perform source data validation as required by the sponsor.
- Prepare monitoring reports and letters per IQVIA Biotech SOP timelines.
- Document accountability, stability, and storage of clinical trial materials.
- Perform investigational product inventory.
- Review clinical data quality and integrity through in-house review and on-site source verification.
- Work with sites to resolve data queries and ensure robust data.
- Review protocols, eCRFs, study manuals, and related documents as requested.
- Serve as the primary contact between IQVIA Biotech and investigators.
- Coordinate correspondence and ensure timely transmission of clinical data and technical reporting.
- Assist with and attend Investigator Meetings.
- Attend study-related, company, departmental, and external meetings as required.
- Ensure all study deliverables are completed per IQVIA Biotech and study timelines.
- Conduct Field Evaluation Visits and field training of CRAs.
Requirements
- Minimum of 2 years experience as a CRA.
- Experience in monitoring and/or coordinating clinical trials required.
- Oncology experience needed.
- Able to handle several priorities within multiple, complex trials.
- Able to reason independently and recommend specific solutions in clinical settings.
- Able to work independently, prioritize, and work within a matrix team environment.
Skills
- Strong knowledge of clinical research process.
- Working knowledge of all functional areas of clinical trials.
- Medical terminology knowledge.
- Excellent written and verbal communication skills.
- Ability to form productive professional relationships internally, cross-functionally, and externally.
- Knowledge of current GCP/ICH guidelines.
Location
- United Kingdom
Work Type
- Freelance
- Travel needed across the UK for site visits
Experience Level
- Minimum of 2 years experience as a CRA
About the Company
- IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
- We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
- Learn more at https://jobs.iqvia.com
Equal Opportunity
- IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
- All information and credentials submitted in your application must be truthful and complete.
- Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
- We appreciate your honesty and professionalism.