Clinical Research Associate II

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

Job summary

A leading company in clinical research is looking for a Clinical Research Associate II to join their Dartford team. The role offers a chance to work in a collaborative environment while handling vital responsibilities like site coordination and compliance management. Ideal candidates will possess relevant educational qualifications, experience, and excellent communication skills, enhancing their career in a rewarding industry.

Benefits

Training and development opportunities

Competitive compensation

Opportunities for hybrid or fully remote work

Qualifications

• Requirement to travel domestically and internationally (up to 8 days per month).
• Previous CRA experience with knowledge of Medical Devices.
• Proficient in clinical investigation procedures.

Responsibilities

• Setting up and coordinating clinical investigations.
• Performing monitoring and site closure visits.
• Ensuring compliance with approved protocols and regulatory requirements.

Skills

Attention to detail

Communication

Teamwork

Education

Master’s degree in life sciences, nursing, or scientific discipline

Tools

Computer systems and software

Job description

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Clinical Research Associate II, Dartford

Client:

Location: Dartford, 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, creating 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 investigation procedures
• 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 approved protocols, Avania SOPs, GCP/ISO14155, and regulatory requirements

Ideal candidates will have:

• A Master’s degree in life sciences, nursing, or a scientific discipline
• Previous 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 systems and software
• Excellent communication and training skills
• Team-oriented and resilient under stress

We offer:

• The chance to work in a dynamic, innovative, and rewarding industry
• A collaborative global team with opportunities to learn from experts across various fields
• Training and development opportunities to support your career growth
• Competitive compensation and benefits (details shared during the interview)
• Travel opportunities for some roles
• Options for hybrid or fully remote work arrangements

Join us at Avania and take the next step in your career.