CRA II - RWE

IQVIA; Dublin; On-site; EUR 45,000 - 60,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate II to support Phase 3b and Phase 4 studies across therapeutic areas. The CRA will cover sites across the UK & Ireland, performing initiation, monitoring and close-out visits in accordance with GCP/ICH guidelines.

This role involves coordinating with sites to drive subject recruitment and ensuring high-quality data collection. Ideal candidates have 1–2 years of on-site monitoring experience, a life-sciences degree, and strong knowledge of regulatory

Qualifications

• 1–2 years of on-site monitoring experience.
• Degree in scientific discipline or health care or equivalent.
• Good knowledge of GCP and ICH guidelines.
• Ability to establish and maintain effective working relationships with coworkers and clients.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per GCP/ICH and contracted scope.
• Drive and track subject recruitment plans to support project timelines.
• Administer protocol training and establish regular communication with sites.
• Evaluate site practices and escalate quality issues as needed.
• Manage study progress: regulatory submissions, recruitment, CRF completion, data queries; may assist start-up.
• Ensure TMF/ISF documents are complete and filed per regulatory requirements.
• Document site management activities and submit visit reports and follow-up communication.
• Collaborate with study team members for project execution.

Skills

On-site monitoring

Regulatory knowledge

Stakeholder management

Communication

Education

Bachelor's degree in life sciences

Job description

Join IQVIA on our mission to accelerate innovation for a healthier world!

IQVIA UK’s RWE team is seeking a Clinical Research Associate II to support Phase 3b and Phase 4 studies across a diverse range of therapeutic areas. The CRA will cover sites across UK & Ireland, with 6-7 site visits per month.

Why join IQVIA?

Community

collaborate with diverse teams and contribute to meaningful work that improves lives.

Development

access tailored learning and development to grow your skills and advance your career.

Flexibility

enjoy a supportive environment that helps you balance work and life.

Recognition

ee celebrated for your contributions and supported in reaching your goals.

Well-being

benefit from country-specific programs that support your health and happiness.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• 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.

Requirements

• Requires at least 1-2 years of on-site monitoring experience.
• Degree in scientific discipline or health care or equivalent industry experience.
• 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.
• Ability to establish and maintain effective working relationships with coworkers and clients.

Please note this position cannot offer visa sponsorship, candidates must hold right to work in UK & Ireland.

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

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.