Clinical Research Associate - North UK

TN United Kingdom; Manchester; On-site; GBP 35,000 - 55,000; Full time

Job summary

Join a forward-thinking company as a Clinical Research Associate, where you will play a pivotal role in managing clinical trial sites across Scotland and Northern England. In this dynamic position, you will ensure compliance with high-quality standards while serving as the main communication link between trial sites and sponsors. You will leverage your expertise in clinical trial monitoring and risk-based quality management to support innovative drug development programs. This role offers the opportunity to work in a collaborative environment that values your contributions and prioritizes your well-being, making a real impact in the field of clinical research.

Benefits

Bonus Scheme

Generous Pension Contributions

Private Medical Insurance

Wellness Program

Life and Disability Insurance

Inclusive Culture

Qualifications

• 2+ years of experience in monitoring clinical trials independently.
• Knowledge of ICH GCP methodology and trial management activities.

Responsibilities

• Manage clinical trial sites ensuring compliance with standards.
• Conduct monitoring visits and follow-up activities.

Skills

Clinical Trial Monitoring

ICH GCP Compliance

Risk-Based Quality Management

Communication Skills

Electronic Clinical Trial Systems

Education

Degree in Life Science or Nursing

Job description

The position

As a Clinical Research Associate, you will manage clinical trial sites to ensure high-quality standards in accordance with the Company’s policies and procedures, relevant legislation, and ICH GCP requirements, while maintaining the standards of the Novo Nordisk Way. You will serve as the main communication link between the site and the sponsor. In this role, you will report to the Regional Clinical Research Manager for the North team. Your key responsibilities will include:

1. Completing clinical trial site monitoring visits, reports, and follow-up activities.
2. Providing support and acting as a local expert for systems or knowledge areas, sharing best practices for the team's benefit.
3. Conducting risk-based quality management of sites in accordance with protocol, monitoring plan, SOPs, relevant legislation, and ICH-GCP guidelines.
4. Supporting the Local Trial Manager as needed and providing line of business support.

Qualifications

To succeed in this role, you should possess:

• A degree in life science or nursing (or equivalent, desirable).
• At least 2 years of experience and success in independently monitoring clinical trials in accordance with ICH GCP methodology.
• Experience in managing trial management activities for commercial clinical trials across all phases (1-4).
• Expertise in electronic clinical trial systems.
• Availability to travel approximately 30% of the time throughout Scotland and Northern England.

About the department

Our Clinical Development Centers (CDCs), part of the Clinical, Medical, and Regulatory Departments, are the backbone of clinical trials and benefit from strengthened partnerships and launches. We conduct clinical trials in over 50 countries worldwide, collaborating closely with our affiliates, regions, and global teams. You will be part of a large, resourceful development team playing a crucial role in Novo Nordisk's ambitious drug development programs. The center comprises around individuals, overseeing 30% of all clinical trial patients in North West Europe.

Working at Novo Nordisk

Novo Nordisk values its people, recognizing that life is non-linear and balancing different career stages is challenging. We accommodate diverse life situations, always prioritizing people. We appreciate the unique skills each employee brings and strive to bring out their best. Working at Novo Nordisk means contributing to something bigger than ourselves—collectively, we go further and aim to be life-changing.

What We Offer

• Bonus: We reward success through our bonus scheme when goals are achieved.
• Workplace: Field-based.
• Pension: A leading pension scheme with generous employer contributions.
• Wellness: Access to an award-winning Wellness program, including Private Medical Insurance, the Lifeworks App, and wellbeing initiatives.
• Insurances: Private medical, life, and disability insurance for all colleagues.
• Inclusive culture: A culture of care, support, and respect, committed to safety and transparency, empowering individuals to excel.

Application support

We are an equal opportunity employer committed to an inclusive recruitment process. If you have a disability or are neurodivergent and require adjustments during the application and selection process, please email us. Include your name, the role you are interested in, and the type of adjustment needed.