Clinical Research Associate II (CRA II)

IQVIA LLC; Swillington; On-site; GBP 30,000 - 50,000; Full time

Job summary

IQVIA Biotech in the United Kingdom is seeking an experienced on-site Clinical Monitor to oversee oncology studies. You will conduct site visits, ensure protocol adherence, and maintain TMF/ISF documentation while coordinating with site staff and the study team.

The role requires 1 year of on-site monitoring experience, strong knowledge of GCP/ICH guidelines, and excellent English communication. A scientific or healthcare degree is preferred, with proficiency in MS Office and a willingness to

Qualifications

• Minimum of 1 year on-site monitoring experience.
• Experience monitoring Oncology studies is required.
• Knowledge of GCP and ICH guidelines.
• Proficient in English with strong communication skills.
• Bachelor's degree in scientific discipline or healthcare.

Responsibilities

• Perform site monitoring visits in line with GCP/ICH and contract scope.
• Drive and track subject recruitment plans to enhance predictability.
• Administer protocol training to sites and maintain communication.
• Evaluate study site quality and regulatory compliance; escalate issues.
• Manage progress: regulatory submissions, recruitment, CRFs, data queries; may support start-up.
• Maintain TMF/ISF documentation and site files.
• Create and maintain site management documentation including visit reports and follow-up letters.
• Collaborate with study team for project execution support.
• Support development of site recruitment plans per site; may handle site finances per agreement.

Skills

Site monitoring

GCP/ICH knowledge

Communication skills

English proficiency

MS Office

Education

Bachelor's Degree in scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

PowerPoint

iPhone/iPad usage

Job description

• 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) verify that the Investigator's Site File (ISF) is maintained in accordance with GCP / ICH 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.
• Minimum of 1 year of experience of on-site monitoring experience
• Experience monitoring Oncology studies is a must
• Bachelor's Degree in scientific discipline or health care preferred
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Basic 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, 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.

Join IQVIA Biotech - Where Innovation Meets Impact

At IQVIA Biotech, we specialize in partnering with smaller biotech and emerging biopharma companies, creating a uniquely dynamic and fast-paced environment. Here, you won't just be part of the process-you'll be at the forefront of it. You'll gain early insights into groundbreaking therapies and novel diseases, often before they reach the broader scientific community. If you're passionate about innovation and eager to make a real difference in the world of biotech, this is your opportunity to thrive., 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.