Clinical Research Associate II

JR United Kingdom; Basildon; Hybrid; GBP 35,000 - 55,000; Full time

Job summary

A leading global company is seeking a Clinical Research Associate II to join their innovative team in a remote-based role in the UK. Ideal candidates will bring strong qualifications in life sciences and proven experience in CRA roles to ensure the highest standards in clinical investigations. The position offers competitive compensation, professional growth opportunities, and a dynamic work environment that fosters collaboration.

Benefits

Opportunities for professional growth, training, and development

Competitive compensation and benefits

Travel opportunities for some roles

Hybrid and fully remote work options

Qualifications

• Master's degree required.
• CRA role experience, preferably with Medical Devices.
• Up to 8 days of travel per month expected.

Responsibilities

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

Skills

Accuracy

Attention to detail

Communication

Training skills

Team-oriented

Resilience under stress

Education

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

Tools

Computer systems and software proficiency

Job description

Social network you want to login/join with:

Clinical Research Associate II, Basildon

Client:

Location: Basildon, 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 CRA II, your responsibilities will include:

• Setting up and coordinating clinical investigations
• Training study sites on conducting investigations
• Performing monitoring and site closure visits
• Ensuring the rights and well-being of human subjects are protected
• Verifying the accuracy, completeness, and verifiability of clinical data against source documents
• Ensuring compliance with protocols, SOPs, GCP/ISO14155, and regulatory requirements

Ideal candidates will have:

• A master's degree in life sciences, nursing, or a scientific 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 with computer systems and software
• 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 global team fostering collaboration and expertise sharing
• Opportunities for professional growth, training, and development
• Competitive compensation and benefits (details provided during interviews)
• Travel opportunities for some roles
• Hybrid and fully remote work options — ask us for details

When you want to advance your career, choose Avania.