Research Associate

Iqvia Cfsp; Bracknell; In loco; GBP 32.000 - 46.000; Tempo pieno

Vantaggi offerti da questo lavoro

World-class training

Professional development

Career advancement opportunities

Descrizione del lavoro

IQVIA cFSP is seeking experienced Clinical Research Associates in the United Kingdom to perform site monitoring visits in accordance with GCP and ICH guidelines. You will work with sites to drive subject recruitment, administer protocol training, and ensure timely, compliant data collection.

Travel to sites is required, and you will track regulatory submissions and data queries while maintaining site documentation.

Competenze

• Minimum 18 months of independent on-site monitoring.
• Experience managing multiple trials across diverse investigative sites.
• Strong knowledge of GCP and ICH guidelines.
• Life science degree or equivalent industry experience.
• Willingness to travel to study sites.

Mansioni

• Conduct site monitoring visits per contracted scope and regulatory requirements.
• Collaborate with sites to recruit and enroll subjects per project needs.
• Provide protocol and study training to assigned sites and maintain communication.
• Assess quality of site practices and escalate issues as needed.
• Track regulatory submissions, approvals, enrollment, CRF completion and data queries.
• Maintain TMF/ISF documentation and visit reports.
• Collaborate with study team for project execution.

Conoscenze

On-site monitoring

Protocol management

GCP knowledge

ICH knowledge

Travel flexibility

Formazione

Life science degree

Descrizione del lavoro

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

• A minimum of 18 months of independent on‑site monitoring
• You have successfully managed multiple clinical trial protocols across diverse investigative sites.
• In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Life science degree educated or equivalent industry experience
• Flexibility to travel to sites

IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.

With access to world‑class training and professional development, we'll give you the tools you need to create the career you want.

Why IQVIA?

• IQVIA is recognized as #1 in its category on the 2026 Fortune® World's Most Admired Companies list for the fifth consecutive year!
• We offer genuine career development opportunities for those who want to grow as part of the organization.
• The chance to work on cutting edge medicines at the forefront of new medicines development.
• IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive.
• Next generation clinical development!, 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

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.