Clinical Research Associate II

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

Job summary

A leading company in clinical operations seeks a Clinical Research Associate II to join their dynamic team. This remote-based role in Birmingham involves setting up clinical investigations, ensuring verifiable data, and adhering to comprehensive compliance measures. Candidates should have a master's degree in a life sciences discipline and previous experience in a similar role. The position offers competitive compensation, opportunities for career growth, and a collaborative work environment.

Benefits

Competitive compensation and benefits package

Opportunities for travel in some roles

Hybrid and fully remote work options

Career growth opportunities

Training and development support

Qualifications

• Master's degree in life sciences, scientific, or nursing discipline required.
• Prior experience in CRA role preferred with Medical Devices knowledge.
• Availability to travel domestically and internationally (up to 8 days per month) required.

Responsibilities

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

Skills

Accuracy

Excellent communication skills

Team player

Stress resilience

Education

Life sciences master's degree

Tools

Computer and software systems

Job description

Social network you want to login/join with:

Clinical Research Associate II, Birmingham

Client:

Location:

Birmingham, United Kingdom

Job Category:

Other

EU work permit required:

Yes

Job Views:

5

Posted:

26.06.2025

Expiry Date:

10.08.2025

Job Description:

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

Continued investment in our global clinical operations team creates this career opportunity for a CRA II to join us in a remote-based role in the UK.

As a Clinical Research Associate II - CRA II, your role will involve:

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

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

• Life sciences master's degree, scientific or nursing discipline
• Prior experience in a CRA role with knowledge of Medical Devices
• Accuracy
• Availability to travel domestically and internationally (up to 8 days per month)
• Proficiency in computer and software systems
• Excellent communication skills and the ability to train others
• Team player
• Stress resilience

We offer:

• The opportunity to work in an innovative, fast-growing, and rewarding industry
• A dynamic and enthusiastic global team fostering collaboration and expertise sharing
• Knowledge exchange and career growth opportunities, supported by training and development
• Competitive compensation and benefits package (details shared during the interview)
• Opportunities for travel in some roles
• Information about our hybrid and fully remote work options

When you need to advance your career, it takes Avania