Clinical Research Associate II

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

Job summary

A leading company in the clinical research sector is seeking a Clinical Research Associate II to enhance their global operations team. This remote-based role offers the candidate a chance to coordinate clinical investigations, train study sites, and ensure the protection of human subjects. Ideal candidates will have a master's degree in a life science field and relevant CRA experience. In return, the company provides competitive rewards, collaborative team dynamics, and opportunities for professional growth.

Benefits

Training and development opportunities for career growth

Competitive compensation and benefits

Hybrid and fully remote work options

Qualifications

• Prior experience in a CRA role 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 conducting clinical investigations.
• Performing monitoring and site closure visits.

Skills

Attention to detail

Communication skills

Team-oriented mindset

Stress resilience

Education

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

Tools

Computer and software systems proficiency

Job description

Social network you want to login/join with:

Clinical Research Associate II, Southampton

Client:

Location: Southampton, 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 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 performing 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 current protocol, Avania SOPs, GCP/ISO14155, and regulatory requirements

Ideal candidates will have:

• A master's degree in life sciences, nursing, or a related scientific discipline
• Prior experience in a CRA role with knowledge of Medical Devices
• Attention to detail and accuracy
• Availability to travel domestically and internationally (up to 8 days per month)
• Proficiency with computer and software systems
• Excellent communication skills and ability to train others
• Team-oriented mindset
• Stress resilience

We offer:

• The chance to work in an innovative, fast-growing industry
• A dynamic, collaborative global team with opportunities to learn from experts
• Training and development opportunities for career growth
• Competitive compensation and benefits (details shared during interview)
• Travel opportunities for some roles
• Hybrid and fully remote work options — ask us for details

Join us at Avania to advance your career!