At a Glance
- Tasks: Conduct site monitoring visits and ensure compliance with clinical research regulations.
- Company: Join IQVIA, a leader in clinical research and healthcare innovation.
- Benefits: Flexible working, career development, and well-being support for a balanced life.
- Other info: Award-winning workplace with opportunities for mentorship and growth.
- Why this job: Make a real impact on health innovation while advancing your career.
- Qualifications: 2 years of monitoring experience and a degree in a scientific discipline.
The predicted salary is between 30000 - 40000 £ 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 experienced Clinical Research Associates across the UK & Ireland.
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 Companies™ 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 2 years on-site monitoring experience of interventional studies
- 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
- Full driving license and access to vehicle required 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!
Clinical Monitoring Associate (Cheetham Hill) in Manchester employer: IQVIA
At IQVIA, we pride ourselves on being an exceptional employer, offering genuine career development opportunities and a supportive work culture that prioritises your well-being. With flexible working arrangements, mentorship through Employee Resource Groups, and recognition as one of the 'Best Places to Work in the UK', we empower our Clinical Monitoring Associates in Cheetham Hill to thrive both professionally and personally while making a meaningful impact in the healthcare sector.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Monitoring Associate (Cheetham Hill) in Manchester
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Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for the Clinical Monitoring Associate (Cheetham Hill) at IQVIA, 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 Clinical Monitoring Associate (Cheetham Hill) at IQVIA. 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!
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How to prepare for a job interview at IQVIA
✨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.
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