Clinical Research Associate II

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

Job summary

A leading clinical operations team is seeking a Clinical Research Associate II to join in a remote-based role. The CRA II will oversee clinical investigations, ensure compliance, and support site training. This position offers growth opportunities in a fast-paced environment, along with competitive compensation and the option for hybrid work.

Benefits

Training and development opportunities

Competitive compensation and benefits

Hybrid and fully remote work options

Travel opportunities for some roles

Qualifications

• Master's degree in relevant field required.
• Experience as a Clinical Research Associate preferred.
• Proficient in computer systems and software.

Responsibilities

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

Skills

Accuracy

Attention to detail

Excellent communication

Team player attitude

Stress resilience

Education

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

Tools

Computer and software systems

Job description

Social network you want to login/join with:

Clinical Research Associate II, Northampton

Client:

Location:

Northampton, 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 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 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 respected
• 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

Ideal candidates will have:

• A master's degree in life sciences, nursing, or a related scientific discipline
• Previous 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
• A team player attitude
• Stress resilience

We offer:

• The chance to work in an innovative, fast-growing, and rewarding industry
• A dynamic global team fostering collaboration and knowledge sharing
• Training and development opportunities for career growth
• Competitive compensation and benefits (details shared during interviews)
• Travel opportunities for some roles
• Hybrid and fully remote work options available

Join us to advance your career with Avania.