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Clinical Research Associate 2

IQVIA Argentina

Reading

On-site

GBP 30,000 - 50,000

Yesterday
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Job summary

An innovative organization is looking for a Clinical Research Associate 2 to join their mission of creating a healthier world. This role offers a supportive environment with collaborative teams and numerous career growth opportunities. As a CRA, you will be responsible for site management and monitoring, ensuring adherence to Good Clinical Practice and ICH guidelines. If you're passionate about making an impact in clinical research and enjoy working in a dynamic setting, this position could be your next career step. Embrace the chance to learn and grow while contributing to meaningful projects.

Benefits

Supportive leadership

Collaborative teams

Technology-enabled resources

Career growth opportunities

Qualifications

  • Minimum 18 months of independent on-site monitoring experience.
  • In-depth knowledge of GCP and ICH guidelines required.

Responsibilities

  • Manage and monitor sites including selection and initiation.
  • Drive and track subject recruitment plans with sites.
  • Provide training on protocols and maintain visit reports.

Skills

Site management

Monitoring

Subject recruitment

Protocol training

Good Clinical Practice (GCP)

International Conference on Harmonization (ICH)

Education

Life science degree

Equivalent industry experience

Job description

IQVIA are seeking a Clinical Research Associate 2 in the UK to join us on our mission to help create a healthier world.

Excellent opportunity for CRAs who would value:

  • Supportive leadership and collaborative teams
  • A variety of career opportunities to allow you to grow as we grow
  • Technology-enabled resources that make doing your job more efficient

Responsibilities

  • Site management and monitoring (site selection, site initiation, routine monitoring and close-out visits)
  • Working with sites to adapt, drive and track subject recruitment plan
  • Providing protocol and study training to assigned sites
  • Creating and maintaining monitoring visit reports and action plans

Requirements

  • Experience of independent on-site monitoring (18 months minimum)
  • 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!

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