Clinical Research Associate II

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

Job summary

Avania is seeking a Clinical Research Associate II for a remote-based role in the UK. The successful candidate will oversee clinical investigations, train sites, and ensure data accuracy, compliance with regulations, and the well-being of subjects. This opportunity offers professional growth in a fast-paced, innovative industry with potential for hybrid or fully remote work.

Benefits

Competitive salary and benefits

Opportunities for growth and development

Training and career advancement

Travel opportunities

Options for hybrid or fully remote work

Qualifications

• Master's degree in life sciences, scientific or nursing discipline.
• Experience in a CRA role with Medical Device knowledge preferred.
• Willingness to travel domestically and internationally.

Responsibilities

• Set up and coordinate clinical investigations.
• Train study sites on conducting clinical investigations.
• Monitor clinical sites and ensure data integrity.

Skills

Accuracy

Attention to detail

Communication

Team-oriented

Resilience under stress

Proficiency in computer systems

Education

Master's degree in life sciences or related field

Job description

Social network you want to login/join with:

Clinical Research Associate II, Colchester

Client:

Location: Colchester, 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 respected
• 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 have:

• A master's degree in life sciences, a scientific or nursing discipline
• Experience in a CRA role 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 and resilient under stress

We offer:

• The chance to work in an innovative, fast-growing industry
• A dynamic, collaborative global team with opportunities for growth and development
• Training and career advancement opportunities
• Competitive salary and benefits (details shared during interview)
• Travel opportunities in some roles
• Options for hybrid or fully remote work

Join us at Avania to advance your career.