Clinical Research Associate II

JR United Kingdom; High Wycombe; Remote; GBP 30,000 - 50,000; Full time

Job summary

Avania is seeking a Clinical Research Associate II to enhance their global clinical operations team in a remote role based in the UK. Key responsibilities include coordinating clinical investigations and ensuring regulatory compliance, requiring a Master's degree and prior experience as a CRA. This position offers opportunities for career development within a dynamic and innovative team, with both hybrid and fully remote work options available.

Benefits

Opportunities for career development

Competitive compensation and benefits

Travel opportunities in some roles

Hybrid and fully remote work options available

Qualifications

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

Responsibilities

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

Skills

Attention to detail

Excellent communication

Team player

Stress resilience

Education

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

Tools

Proficiency in computer systems and software

Job description

Social network you want to login/join with:

Clinical Research Associate II, High Wycombe

Client:

Location:

High Wycombe, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

3

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 career opportunity for a CRA II to join us in a remote-based role in the UK.

As a Clinical Research Associate II, your responsibilities 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 with source documents
• Ensuring conduct complies with approved protocols, Avania SOPs, GCP/ISO14155, and regulatory requirements

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

• Master's degree in life sciences, nursing, or related scientific discipline
• Prior CRA experience with knowledge of Medical Devices
• Attention to detail and accuracy
• Availability to travel domestically and internationally (up to 8 days/month)
• Proficiency in 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, collaborative global team with expert colleagues
• Knowledge sharing, training, and career development opportunities
• Competitive compensation and benefits (details shared during interview)
• Travel opportunities in some roles
• Hybrid and fully remote work options available

When you need to advance your career, it takes Avania.