Clinical Research Associate II

JR United Kingdom; Peterborough; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading company in clinical operations, Avania, is looking for a Clinical Research Associate II (CRA II) to join their remote-based team in the UK. This role involves setting up clinical investigations, ensuring compliance with protocols, and protecting the rights of human subjects. The ideal candidate will have a Master’s degree in life sciences and experience in the CRA role, along with strong communication and organizational skills. Enjoy a collaborative work environment with opportunities for innovative career development and travel.

Benefits

Opportunities for innovative career development

Competitive compensation and benefits

Travel opportunities for some roles

Options for hybrid and fully remote work

Qualifications

• Must hold a Master's degree in life sciences or related field.
• Experience in a CRA role and knowledge of Medical Devices is required.
• Must be able to travel domestically and internationally up to 8 days a month.

Responsibilities

• Setting up and coordinating clinical investigations.
• Training study sites on clinical investigations.
• Performing monitoring and site closure visits.

Skills

Accuracy

Attention to detail

Excellent communication

Training skills

Team-oriented

Resilience under stress

Education

Master's degree in life sciences

Nursing or related scientific discipline

Tools

Computer and software systems

Job description

Social network you want to login/join with:

Clinical Research Associate II, Peterborough

Client:

Location: Peterborough, 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 clinical 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 investigation data with source documents
• Ensuring compliance with the approved protocol, Avania SOPs, GCP/ISO14155, and regulatory requirements

We encourage candidates with the following skills and experience to apply:

• Master's degree in life sciences, nursing, or related 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 in computer and software systems
• Excellent communication and training skills
• Team-oriented and resilient under stress

We offer:

• Opportunities to work in an innovative, fast-growing industry
• A collaborative global team with expertise across various fields
• Knowledge sharing, training, and career development opportunities
• Competitive compensation and benefits (details shared during the interview)
• Travel opportunities for some roles
• Options for hybrid and fully remote work arrangements

Advance your career with Avania.