CRA 2 - Single Sponsor Dedicated

IQVIA LLC; Reading; Hybrid; GBP 32,000 - 52,000; Full time

Job summary

IQVIA cFSP (sponsor-dedicated) seeks experienced Clinical Research Associates in the UK. The role involves on-site monitoring and site management to ensure protocol adherence, data quality and regulatory compliance across multiple UK sites.

Responsibilities include initiating and monitoring visits, training site staff, tracking recruitment, and managing trial documentation in TMF/ISF. 1+ year on-site experience preferred; English communication essential.

Qualifications

• Bachelor's degree in scientific discipline or health care.
• At least 1 year of on-site monitoring experience.
• Knowledge of GCP and ICH guidelines.
• Good written and verbal English communication.
• Proficient with MS Office and laptop use.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out).
• Support subject recruitment plans and project needs.
• Administer protocol training and maintain site communication.
• Evaluate site practices for protocol compliance and data integrity.
• Track regulatory submissions, recruitment, CRF completion, and data queries.
• Ensure TMF/ISF documentation and site files are up-to-date.
• Collaborate with study team and support start-up activities if needed.

Skills

Site monitoring

Regulatory compliance

Data integrity

Communication skills

English proficiency

Education

Bachelor's degree in science or health care

Tools

MS Word

MS Excel

MS PowerPoint

iPhone/iPad

Job description

## CRA 2 - Single Sponsor DedicatedApplylocations: Reading, Berkshire, United Kingdom: Manchester, United Kingdom: Livingston, West Lothian, United Kingdom: London, United Kingdomtime type: Full timeposted on: Posted 8 Days Agojob requisition id: R1527512**Join Us on Our Mission to Drive Healthcare Forward**IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.**Job Overview** Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.**Essential Functions** • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice. • Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability. • Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues. • Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate. • Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase. • Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation. • Collaborate and liaise with study team members for project execution support as appropriate. • If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis. • If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.**Qualifications** • Bachelor's Degree Degree in scientific discipline or health care preferred. Req • Requires at least 1 of year of on-site monitoring experience. Req • Equivalent combination of education, training and experience may be accepted in lieu of degree. Req • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements. • i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. • Good therapeutic and protocol knowledge as provided in company training. • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). • Written and verbal communication skills including good command of English language. • Organizational and problem-solving skills. • Effective time and financial management skills. • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.**\\*Please note - this role is not eligible for UK visa sponsorship\\***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.comIQVIA 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.