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Clinical Research Associate II

JR United Kingdom

Brighton

Remote

GBP 35,000 - 50,000

Full time

Yesterday
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Job summary

A leading company in clinical research is seeking a Clinical Research Associate II (CRA II) for a remote opportunity in the UK. The role includes coordinating clinical investigations and training sites. Ideal candidates should possess a master's degree in a relevant field and prior CRA experience, offering an innovative workspace with growth opportunities.

Benefits

Opportunities for professional growth and development
Competitive compensation and benefits
Travel opportunities for some roles
Options for hybrid and fully remote work

Qualifications

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

Responsibilities

  • Setting up and coordinating clinical investigations.
  • Training study sites on clinical investigations.
  • Performing monitoring and site closure visits.

Skills

Attention to detail
Communication
Training skills
Team-oriented attitude

Education

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

Tools

Computer and software systems

Job description

Social network you want to login/join with:

Clinical Research Associate II, Brighton

Client:

Location:

Brighton, United Kingdom

Job Category: Other

-

EU work permit required: Yes

Job Views:

4

Posted:

26.06.2025

Expiry Date:

10.08.2025

Job Description:

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

We are investing in our global clinical operations team, creating this 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 the accuracy, completeness, and verifiability of clinical investigation data with source documents
  • Ensuring compliance with the approved protocol, Avania SOPs, GCP/ISO14155, and regulatory requirements

Ideal candidates will have:

  • A master's degree in life sciences, nursing, or a related 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 in computer and software systems
  • Excellent communication and training skills
  • Team-oriented and stress-resilient attitude

We offer:

  • The chance to work in an innovative, fast-growing industry
  • A collaborative, global team with diverse expertise
  • Opportunities for professional growth and development
  • Competitive compensation and benefits (details shared during the interview)
  • Travel opportunities for some roles
  • Options for hybrid and fully remote work

Join us at Avania and take your career to the next level.

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