Clinical Research Associate II

JR United Kingdom; Gloucester; Remote; GBP 30,000 - 45,000; Full time

Job summary

A leading company in clinical research is seeking a Clinical Research Associate II to join their dynamic team in a remote role within the UK. The position involves coordinating clinical investigations, training sites, and maintaining compliance with protocols. Ideal candidates will possess a master's in life sciences and possess strong attention to detail and communication skills, along with previous CRA experience.

Benefits

Competitive compensation and benefits

Training and development opportunities

Opportunities for travel

Options for hybrid and fully remote work

Qualifications

• Previous 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.
• Ensuring compliance with the approved protocol and regulatory requirements.
• Performing monitoring and site closure visits.

Skills

Accuracy

Attention to detail

Communication

Training skills

Team-oriented mindset

Stress resilience

Education

Master's degree in life sciences

Tools

Computer and software systems

Job description

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Clinical Research Associate II, Gloucester

Client:

Location: Gloucester, 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 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 have:

• A master's degree in life sciences, a scientific or nursing discipline
• Previous 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 mindset
• Stress resilience

We offer:

• The chance to work in an innovative, fast-growing, and rewarding industry
• A dynamic, global team that encourages collaboration and knowledge sharing
• Training and development opportunities to advance your career
• Competitive compensation and benefits (details provided during interview)
• Opportunities for travel for some roles
• Options for hybrid and fully remote work

Join us to take your career to the next level with Avania.