At a Glance
- Tasks: Monitor clinical trials, ensuring compliance and quality in oncology research.
- Company: Join IQVIA, a leader in healthcare innovation and research.
- Benefits: Flexible working, well-being support, and career development opportunities.
- Other info: Recognised as a top workplace with excellent growth potential.
- Why this job: Make a real impact in healthcare while advancing your career.
- Qualifications: 3-5 years of monitoring experience and a degree in a scientific discipline.
The predicted salary is between 40000 - 50000 £ per year.
Join IQVIA on our mission to accelerate innovation for a healthier world! IQVIA’s Site Management (full service / multi-sponsor) team is growing and seeking Senior Clinical Research Associates in the UK.
Why IQVIA?
- Genuine career development opportunities to grow as we grow
- AI‐powered career advancement through our internal talent marketplace, Career Connections
- Mentorship opportunities across the organisation via Employee Resource Groups
- Flexible working to assist work–life balance and professional success
- Well‐being support covering your physical, mental, and financial health
Awards
- 2026 "Glassdoor Best Place to Work in the UK"
- #1 in category - 2026 Fortune World’s Most Admired CompaniesTM list (for the FIFTH consecutive year!)
- Brandon Hall Excellence Award for Learning & Development
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 3-5 years on-site monitoring experience of interventional studies
- Degree in scientific discipline / 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
- Full driving license and access to vehicle for travel to sites
Please note - this position is not eligible for visa sponsorship.
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
Senior Clinical Research Associate, Oncology in Manchester employer: IQVIA LLC
At IQVIA, we are committed to fostering a dynamic work environment that prioritises employee growth and well-being. As a Senior Clinical Research Associate in Manchester, you will benefit from flexible working arrangements, comprehensive support for your physical and mental health, and access to AI-driven career advancement tools. Join us and be part of a team recognised as one of the best places to work, where your contributions will help accelerate innovation for a healthier world.
StudySmarter Expert Advice🤫
We think this is how you could land Senior Clinical Research Associate, Oncology in Manchester
✨Get Involved in Local Health Initiatives
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We think you need these skills to ace Senior Clinical Research Associate, Oncology in Manchester
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for the Senior Clinical Research Associate, Oncology at IQVIA LLC, focus on highlighting your clinical experience and any specific training you've undergone. Include any relevant placements or internships you’ve completed, as well as any certifications that bolster your qualifications in human medicine.
Highlight Your Soft Skills:In the field of human medicine, soft skills are just as crucial as technical knowledge. Mention your communication skills, empathy, and teamwork experiences in your CV and cover letter. This shows that you can work well in a clinical setting and with patients, which is super important in this industry!
Tailor Your Cover Letter Thoughtfully:Be sure to personalise your cover letter for the Senior Clinical Research Associate, Oncology at IQVIA LLC. Mention why you’re passionate about human medicine and how you align with the company’s mission. This is your chance to convey your enthusiasm and make a case for why you'll be a valuable addition to the team!
Include Continuing Education:Make sure to mention any ongoing education or courses you’re taking to keep your skills sharp. In human medicine, staying updated with the latest practices is key. It shows you’re dedicated to your field, which employers like IQVIA LLC will definitely appreciate!
How to prepare for a job interview at IQVIA LLC
✨Brush Up on Clinical Knowledge
Since you're aiming for a role in human medicine, make sure you’re sharp on the latest clinical guidelines and practices relevant to the position. Be prepared to discuss case studies or scenarios you might encounter in the role. This will show that you're not just knowledgeable but also ready to apply that knowledge in real-life situations.
✨Demonstrate Soft Skills
In human medicine, technical skills are crucial, but don’t forget to showcase your soft skills like communication, empathy, and teamwork. In your answers, share specific examples of how you've worked effectively with patients or colleagues in the past, as these traits are highly valued in clinical settings.
✨Know Your CV Backwards
As you’re applying for a full-time position, your CV should tell a story. Be ready to discuss every part of it, especially your clinical experiences, the impact you had, and what you learned. Employers want to see how your journey has prepared you for this role, so think of it like you're taking them through your professional narrative.
✨Prepare for Ethical Scenarios
Ethics are a big deal in human medicine, so expect questions that assess your decision-making in tricky situations. Think about how you'd handle ethical dilemmas or patient confidentiality concerns. Prepare a few examples that illustrate your thought process and how you prioritise patient welfare in your decision-making.
