Clinical Research Associate II

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

Job summary

A leading global company is seeking a Clinical Research Associate II to join their innovative team. In this remote position, you will coordinate clinical investigations, ensure data integrity, and support the health and safety of human subjects. This role offers opportunities for professional growth in a collaborative environment, with flexible working options.

Benefits

Opportunities for knowledge exchange and career development

Competitive compensation and benefits

Travel opportunities

Hybrid and fully remote work options

Qualifications

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

Responsibilities

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

Skills

Accuracy

Attention to detail

Communication

Team-oriented mindset

Stress resilience

Education

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

Tools

Computer software systems

Job description

Social network you want to login/join with:

Clinical Research Associate II, Sheffield, South Yorkshire

Client:

Location:

Sheffield, South Yorkshire, 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 and are offering this opportunity for a CRA II to join us in a remote-based role in the UK.

As a 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 protected
• Verifying that clinical investigation data are accurate, complete, and verifiable with source documents
• Ensuring conduct compliance with the approved protocol, Avania SOPs, GCP/ISO14155, and regulatory requirements.

Ideal candidates will have:

• A master's degree in life sciences, nursing, or a scientific discipline
• 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 and training skills
• Team-oriented mindset
• Stress resilience

We offer:

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

Join us at Avania to advance your career.