Clinical Research Associate II

JR United Kingdom; North East; Remote; GBP 40,000 - 60,000; Full time

Job summary

Avania is seeking a Clinical Research Associate II for a remote role in the UK. This position will involve coordinating clinical investigations, training sites, and ensuring compliance with protocols and regulations. The ideal candidate will hold a master's degree and have experience as a CRA, with attention to detail and strong communication skills.

Benefits

Training and development opportunities

Competitive compensation and benefits

Opportunities for travel

Flexible work arrangements (hybrid and fully remote options)

Qualifications

• Master's degree in life sciences or similar.
• Prior experience as a CRA with knowledge of Medical Devices.
• Availability to travel domestically and internationally.

Responsibilities

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

Skills

Attention to detail

Communication skills

Team player

Stress resilience

Proficiency in computer systems

Education

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

Job description

Social network you want to login/join with:

Clinical Research Associate II, Newcastle-upon-Tyne, Tyne and Wear

Client:

Location:

Newcastle-upon-Tyne, Tyne and Wear, 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 and this creates a 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 will include:

• Setting up and coordinating clinical investigations
• Training study sites on performing 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 the conduct of the Clinical Investigation complies with the approved protocol, 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 a scientific discipline
• Prior experience as a CRA 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 skills and ability to train others
• Team player and stress resilient

We offer:

• The opportunity to work in an innovative, fast-growing, and rewarding industry
• A dynamic global team fostering collaboration and knowledge sharing
• Training and development opportunities to support career growth
• Competitive compensation and benefits (details shared during the interview)
• Opportunities for travel and flexible work arrangements (hybrid and fully remote options)

When you need to advance your career, it takes Avania