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IQVIA

Clinical Research Associate

IQVIA

Reading, England, United Kingdom • Penuh Waktu

Jadilah yang pertama mendaftar

Pengalaman
Setiap
Gaji
Lowongan
1
Diposting
2 minggu yang lalu
Mode kerja
Di kantor
Pendidikan
Life sciences degree or equivalent
Kelayakan
Professionals with oncology site monitoring experience, a life sciences degree or equivalent industry experience, and the ability to travel. Candidates must already have the right to work without visa sponsorship.
Melanjutkan
Wajib mendaftar

Tempat Anda akan bekerja

Deskripsi pekerjaan

Role overview

IQVIA’s multi-sponsor Site Management team is looking for a Clinical Research Associate to support its mission of improving health outcomes worldwide. This position focuses on Oncology studies and requires site coverage across the UK.

This opportunity is suited to someone who wants meaningful work, room to grow, and continued learning in a purpose-driven environment.

Key responsibilities

  • Carry out site monitoring activities, including selection, initiation, routine monitoring, and close-out visits, in line with the contracted scope and Good Clinical Practice requirements.
  • Partner with sites to shape, monitor, and improve recruitment plans so study targets are met more reliably.
  • Deliver protocol and study-related training to assigned sites and keep communication channels open to resolve issues and maintain alignment on expectations.
  • Review site conduct and data handling to confirm quality, protocol compliance, and adherence to relevant regulations, escalating any concerns when needed.
  • Track study progress by following regulatory submissions and approvals, recruitment and enrollment activity, CRF completion and submission, and data query creation and resolution; provide support during start-up where required.
  • Make sure essential site documents are filed in the Trial Master File and that the Investigator’s Site File is kept current in line with GCP and local regulatory rules.
  • Prepare and maintain records for site management, monitoring findings, and follow-up actions, including visit reports, follow-up letters, and other study documents.
  • Work closely with study team members to support smooth project delivery.

Requirements

  • Previous experience independently monitoring oncology studies on-site, including unblinded trials.
  • Strong working knowledge of Good Clinical Practice and ICH guidelines.
  • A life sciences degree or an equivalent level of industry experience.
  • Willingness and flexibility to travel to sites as needed.
  • Applicants must not require visa sponsorship for this position.

About the employer

IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for life sciences and healthcare organizations. The company focuses on connecting data, science, and expertise to support the development and launch of innovative treatments that can improve patient and population health.

Important notice

IQVIA states that it follows a strict integrity policy in hiring. All details, qualifications, and statements provided during the application process must be accurate and complete. Any false or incomplete information may lead to disqualification during recruitment or termination later, where permitted by law.

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