Experienced Clinical Research Associate

Nanosep AB; Reading; On-site; GBP 40,000 - 70,000; Full time

Job summary

An established industry player is seeking an experienced Clinical Research Associate to join their mission in advancing healthcare. This role involves managing site activities, ensuring compliance with Good Clinical Practice, and mentoring junior team members. You will play a vital role in driving subject recruitment and maintaining high standards in clinical trials. If you're passionate about making a difference in patient outcomes and thrive in a dynamic environment, this opportunity is perfect for you. Join a diverse team dedicated to innovation and impact in the healthcare sector.

Qualifications

• Experience of independent on-site monitoring in the UK.
• Flexibility to travel to sites as required.

Responsibilities

• Site management and monitoring in partnership with a single-sponsor.
• Providing protocol and study training to assigned sites.

Skills

Site management

Good Clinical Practice (GCP)

International Conference on Harmonization (ICH) guidelines

Subject recruitment

Education

Life science degree

Job description

Join to apply for the Experienced Clinical Research Associate role at Nanosep AB

6 days ago Be among the first 25 applicants

Join to apply for the Experienced Clinical Research Associate role at Nanosep AB

IQVIA Clinical FSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK to join us on our mission to help create a healthier world.

By joining our diverse, global team, youll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.

Responsibilities

• Site management and monitoring (site selection, site initiation, routine monitoring and close-out visits) in partnership with a single-sponsor.
• Working with sites to adapt, drive and track subject recruitment plan.
• Providing protocol and study training to assigned sites.
• Creating and maintain monitoring visit reports and action plans.
• If appropriate, co-monitoring, training and mentoring junior members of the team.
  
  

Requirements

• Experience of independent on-site monitoring in the UK.
• 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.
  
  

Apply today and forge a career with greater purpose, make an impact, and never stop learning!

Please note - this role is not eligible for UK visa sponsorship

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 https://jobs.iqvia.com

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

EEO Minorities/Females/Protected Veterans/Disabled

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Science

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