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Clinical Research Associate II

JR United Kingdom

Warrington

Remote

GBP 30,000 - 50,000

Full time

Yesterday
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Job summary

A leading company in clinical operations is hiring a Clinical Research Associate II for a remote role in the UK. Responsibilities include coordinating clinical investigations and ensuring compliance. Ideal candidates should possess a Master's degree and CRA experience, with strong communication skills. Career growth opportunities and competitive compensation are offered.

Benefits

Training and development opportunities
Competitive compensation and benefits
Opportunities to work in an innovative environment
Hybrid and fully remote work options

Qualifications

  • Prior CRA experience with knowledge of Medical Devices.
  • Availability to travel domestically and internationally (up to 8 days per month).

Responsibilities

  • Setting up and coordinating clinical investigations.
  • Training study sites on clinical investigations.
  • Performing monitoring and site closure visits.
  • Ensuring compliance with approved protocols and regulatory requirements.

Skills

Accuracy
Attention to detail
Excellent communication
Team player
Stress resilience
Training skills

Education

Master's degree in life sciences, nursing, or a scientific discipline

Tools

Computer systems and software proficiency

Job description

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Clinical Research Associate II, Warrington, Cheshire

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Client:
Location:
Job Category:

Other

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EU work permit required:

Yes

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Job Views:

5

Posted:

26.06.2025

Expiry Date:

10.08.2025

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Job Description:

Avania is hiring a Clinical Research Associate II (CRA II)

We are investing in our global clinical operations team and are offering this career opportunity for a CRA II to join us in a remote-based role in the UK.

As a CRA II, your responsibilities will include:

  • Setting up and coordinating clinical investigations
  • Training study sites on clinical investigations
  • Performing monitoring and site closure visits
  • Ensuring the rights and well-being of human subjects are respected
  • Verifying that clinical investigation data are accurate, complete, and verifiable with source documents
  • Ensuring compliance with the approved protocol, Avania SOPs, GCP/ISO14155, and regulatory requirements

Candidates with the following skills and experience are encouraged to apply:

  • Master's degree in life sciences, nursing, or a scientific discipline
  • Prior CRA experience with knowledge of Medical Devices
  • Accuracy and attention to detail
  • Availability to travel domestically and internationally (up to 8 days per month)
  • Proficiency with computer systems and software
  • Excellent communication and training skills
  • Team player and stress resilient

We offer:

  • Opportunities to work in an innovative, fast-growing industry
  • A dynamic global team fostering collaboration and expertise sharing
  • Training and development opportunities for career growth
  • Competitive compensation and benefits (details shared during the interview)
  • Travel opportunities in some roles
  • Hybrid and fully remote work options available

When you want to advance your career, choose Avania.

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