Clinical Research Associate II

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

Job summary

Avania is seeking a Clinical Research Associate II for its global clinical operations team, offering a remote-based role in the UK. The successful candidate will be responsible for coordinating clinical investigations, ensuring compliance, and providing training. Ideal candidates will possess a relevant master's degree and have CRA experience, along with strong communication and attention to detail. This opportunity includes competitive compensation, benefits, and potential for professional growth within a dynamic team.

Benefits

Knowledge exchange, training, and development opportunities

Competitive compensation and benefits

Travel opportunities in some roles

Dynamic, collaborative global team

Hybrid and fully remote work options

Qualifications

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

Responsibilities

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

Skills

Accuracy

Attention to detail

Communication

Team-oriented attitude

Stress resilience

Education

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

Tools

Computer and software systems

Job description

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Clinical Research Associate II, Nottingham

Client:

Location:

Nottingham, United Kingdom

Job Category:

Other

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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, 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 - 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 respected
• Verifying that clinical investigation data are accurate, complete, and verifiable with source documents
• Ensuring compliance with the current protocol, Avania SOPs, GCP/ISO14155, and regulatory requirements

Ideal candidates will have:

• A master's degree in life sciences, nursing, or a scientific discipline
• Prior 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
• Team-oriented attitude
• Stress resilience

We offer:

• The chance to work in an innovative, fast-growing industry
• A dynamic, collaborative global team with opportunities for professional growth
• Knowledge exchange, training, and development opportunities
• Competitive compensation and benefits (details shared during the interview)
• Travel opportunities in some roles
• Hybrid and fully remote work options available

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