Senior Clinical Research Associate

Meeveem Limited; Reading; On-site; GBP 65,000 - 90,000; Full time

Benefits offered by this job

Competitive salary and incentives

Health and wellbeing programmes

Retirement and pension plans

Life assurance and disability coverage

Learning and development opportunities

Career progression

Job summary

ICON Plc is seeking an experienced Senior Clinical Research Associate (CRA) based in the UK with extensive oncology CRA background. The role focuses on site monitoring, data integrity, and ensuring regulatory compliance across trials, with substantial travel.

You will collaborate with cross-functional teams, train site staff, and manage multiple sites while maintaining high standards of GCP and trial conduct. A 60% travel expectation and a strong clinical trial toolkit are required.

Qualifications

• Advanced degree in life sciences, nursing, or medicine.
• 7+ years' experience as a CRA.
• At least 2 years' experience working on Oncology studies.
• Experience monitoring multiple sites and projects.
• Proficiency in clinical trial software and tools.
• Excellent communication and stakeholder management.
• Willingness to travel 60% (international and domestic).

Responsibilities

• Monitor clinical trial sites for protocol and GCP compliance.
• Conduct site visits and support trial execution.
• Collaborate with cross-functional teams for data collection and reporting.
• Provide training to site staff and other CRAs.
• Build relationships with site personnel and stakeholders.

Skills

Site monitoring

GCP compliance

Data integrity

Regulatory knowledge

Stakeholder management

Oncology experience

Travel readiness

Education

Advanced degree in life sciences/medicine

Tools

Clinical trial software

Job description

Senior CRA

ICON is a global healthcare intelligence and clinical research organization united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organization, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

Role: Senior CRA (Must have 7 years' experience minimum working as a CRA)

Location: Must be based in the UK - nationwide travel

Sponsorship: Fully sponsor dedicated

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
• Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
• Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
• Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
• Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile

• Advanced degree in a relevant field such as life sciences, nursing, or medicine.
• Extensive experience as a Clinical Research Associate, (7+ years' minimum required) with a strong understanding of clinical trial processes and regulatory requirements.
• Must have at least 2 years' experience working on Oncology studies.
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
• Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
• Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
• Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request.