Clinical Monitoring Associate (Salford) in Manchester

Clinical Monitoring Associate (Salford) in Manchester

Manchester Full-Time 30000 - 40000 £ / year (est.) No working from home possible
IQVIA

At a Glance

  • Tasks: Monitor clinical sites and support Oncology studies across the UK.
  • Company: Join IQVIA, a leader in clinical research and healthcare intelligence.
  • Benefits: Gain valuable experience, make an impact, and enjoy continuous learning opportunities.
  • Other info: Flexible travel required; this role is not eligible for visa sponsorship.
  • Why this job: Be part of a mission to create a healthier world through innovative medical treatments.
  • Qualifications: Experience in Oncology monitoring and knowledge of GCP and ICH guidelines required.

The predicted salary is between 30000 - 40000 £ per year.

IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world. The Clinical Research Associate will support Oncology studies and cover sites across the UK.

Responsibilities

  • Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
  • 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

  • Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
  • 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 as required.

*Please note - this role is not eligible for visa sponsorship.*

Clinical Monitoring Associate (Salford) in Manchester employer: IQVIA

At IQVIA, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and continuous learning. As a Clinical Monitoring Associate in Salford, you will have the opportunity to make a meaningful impact in the field of Oncology while benefiting from comprehensive training and career development programmes. Our commitment to employee growth, coupled with our mission to improve global health outcomes, makes IQVIA a rewarding place to advance your career.

IQVIA

Contact Details:

IQVIA Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Clinical Monitoring Associate (Salford) in Manchester

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We think you need these skills to ace Clinical Monitoring Associate (Salford) in Manchester

Site Monitoring
Good Clinical Practice (GCP)
Oncology Knowledge
Regulatory Compliance
Data Management
Communication Skills
Project Management

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for the Clinical Monitoring Associate (Salford) 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.

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Tailor Your Cover Letter Thoughtfully:Be sure to personalise your cover letter for the Clinical Monitoring Associate (Salford) 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

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Know Your CV Backwards

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