Clinical Research Associate II

JR United Kingdom; Stoke-on-Trent; Remote; GBP 30,000 - 60,000; Full time

Job summary

A leading company in clinical research, Avania, is looking for a Clinical Research Associate II in Stoke-on-Trent. This remote role offers exciting opportunities to set up and coordinate clinical investigations, ensuring regulatory compliance and the well-being of participants. Ideal candidates should have a master's degree and CRA experience, and will enjoy a dynamic team environment with options for professional growth.

Benefits

Professional growth opportunities

Competitive compensation and benefits

Options for hybrid and fully remote work arrangements

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

Excellent communication

Training skills

Team-oriented attitude

Stress resilience

Education

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

Tools

Proficiency in computer and software systems

Job description

Social network you want to login/join with:

Clinical Research Associate II, Stoke-on-Trent

Client:

Location:

Stoke-on-Trent, 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 and are offering this 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 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 compliance with the approved protocol, Avania SOPs, GCP/ISO14155, and regulatory requirements

Ideal candidates will possess:

• A master's degree in life sciences, nursing, or related scientific disciplines
• 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, global team fostering collaboration and expertise sharing
• Opportunities for professional growth, training, and development
• Competitive compensation and benefits (details provided during interviews)
• Potential travel opportunities
• Options for hybrid and fully remote work arrangements

Join us at Avania to advance your career.