Clinical Research Associate II

JR United Kingdom; Oxford; Remote; GBP 35,000 - 50,000; Full time

Job summary

A leading company in the clinical research field is seeking a Clinical Research Associate II to join their team. In this remote-based role in the UK, you'll be responsible for coordinating clinical investigations and ensuring compliance with legal and ethical standards. Ideal candidates will have a master's degree in a relevant field and CRA experience, showcasing attention to detail and excellent communication skills. Join a collaborative, innovative environment with opportunities for knowledge sharing and career development.

Benefits

Career development opportunities

Competitive compensation and benefits

Hybrid and fully remote work options

Qualifications

• Experience as a Clinical Research Associate (CRA) with knowledge of Medical Devices.
• Proficiency in communication and training skills.
• Availability to travel domestically and internationally (up to 8 days/month).

Responsibilities

• Set up and coordinate clinical investigations.
• Perform monitoring and site closure visits.
• Ensure compliance with protocols and regulatory requirements.

Skills

Attention to detail

Communication

Team-oriented

Education

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

Tools

Computer and software systems

Job description

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Clinical Research Associate II, Oxford District

Client:

Location:

Oxford District, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

Job Views:

5

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 protected
• Verifying that clinical investigation data are accurate, complete, and verifiable
• Ensuring compliance with protocols, SOPs, GCP/ISO14155, and regulatory requirements

Ideal candidates will have:

• A master's degree in life sciences, nursing, or a related scientific discipline
• Experience as a CRA with knowledge of Medical Devices
• Attention to detail and accuracy
• Availability to travel domestically and internationally (up to 8 days/month)
• Proficiency in computer and software systems
• Excellent communication and training skills
• Team-oriented and stress-resilient

We offer:

• Opportunities to work in an innovative, fast-growing industry
• A collaborative, global team environment with expert colleagues
• Knowledge sharing and career development opportunities
• Competitive compensation and benefits (details shared during interviews)
• Travel opportunities in some roles
• Hybrid and fully remote work options available

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