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Freelance Clinical Trial Associate

JR United Kingdom

London

Hybrid

GBP 150,000 - 200,000

Full time

2 days ago
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Job summary

An innovative firm is seeking a Freelance Clinical Trial Associate to join their dynamic team in London. This role offers the flexibility of a hybrid work arrangement, allowing you to contribute to groundbreaking clinical research while working with a talented team. As a key player in managing and executing clinical trials, you'll ensure compliance with regulatory standards and support the smooth progress of studies from start-up to close-out. If you're passionate about clinical research and looking for a role that values your expertise, this opportunity is perfect for you!

Qualifications

  • Experience in clinical trial management or similar roles is essential.
  • Strong communication and organizational skills are a must.

Responsibilities

  • Assist in preparing and submitting study documents for trials.
  • Ensure compliance with GCP and regulatory guidelines.

Skills

Clinical Trial Management
Good Clinical Practice (GCP)
Organizational Skills
Communication Skills

Job description

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Freelance Clinical Trial Associate, London
Client:

Barrington James

Location:

London, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

8

Posted:

18.04.2025

Expiry Date:

02.06.2025

Job Description:

Are you a passionate and skilled Clinical Trial Associate looking for a flexible, dynamic role? Join a leading Biotech as a Freelance Clinical Trial Associate and contribute to groundbreaking clinical research while enjoying a hybrid work arrangement!

Role Overview: As a Freelance Clinical Trial Associate (CTA), you'll play a key role in supporting the management and execution of clinical trials. You’ll work with a talented team, ensuring the smooth progress of studies, from start-up through to close-out, all while adhering to regulatory standards.

Location: Work remotely the rest of the time!

Key Responsibilities:

  • Assist in the preparation and submission of study documents.
  • Support the management of clinical trial sites and vendors.
  • Ensure compliance with Good Clinical Practice (GCP) and regulatory guidelines.
  • Maintain study-related documentation and databases.
  • Coordinate and communicate with stakeholders, including monitors, investigators, and clinical teams.

Requirements:

  • Previous experience as a Clinical Trial Associate (CTA) or similar clinical role.
  • Knowledge of clinical trial processes and GCP.
  • Strong organizational and communication skills.
  • Ability to work independently and as part of a team.
  • Availability to be in the office in London for 2 days per week.

Interested? Apply now and be part of an innovative team shaping the future of clinical research!

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