Senior Clinical Research Associate

TN United Kingdom; London; On-site; GBP 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a Freelance Senior Clinical Research Associate with a strong background in ophthalmology, particularly in retinal disorders. This role is pivotal in leading site monitoring activities for innovative gene therapy studies, ensuring compliance with regulatory standards and high-quality execution. Join a dynamic team dedicated to advancing clinical research and making a significant impact on patient care. With a commitment to trust, quality, and sustainability, this opportunity offers a chance to contribute to cutting-edge research in a collaborative environment.

Qualifications

• Experience in clinical trial monitoring within a CRO or pharmaceutical company.
• Strong knowledge of ophthalmology trials and regulatory requirements.

Responsibilities

• Lead site monitoring activities for ophthalmology trials and ensure protocol adherence.
• Manage ethics committee submissions and maintain trial quality.

Skills

Clinical trial monitoring

Ophthalmology expertise

Regulatory compliance

Interpersonal skills

Education

Bachelor's degree in Life Sciences

Job description

Social network you want to login/join with:

Senior Clinical Research Associate, London

col-narrow-left

Client:

TFS HealthScience

Location:

London, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Reference:

6708f4ed5e11

Job Views:

3

Posted:

02.05.2025

Expiry Date:

16.06.2025

col-wide

Job Description:

TFS HealthScience is a global, mid-sized Contract Research Organization (CRO) dedicated to supporting biotechnology and pharmaceutical companies throughout their clinical development journey. We provide full-service capabilities, resourcing, and Functional Service Provider (FSP) solutions to help bring innovative therapies to patients worldwide.

We are currently seeking a Freelance Senior Clinical Research Associate (SCRA) with strong ophthalmology experience, particularly in retinal disorders, based in the UK. This role involves working with a key sponsor on gene therapy and retinal disease studies, ensuring high-quality execution, regulatory compliance, and effective risk-based monitoring.

Please, keep in mind that this is a Freelance role for approximately 0.25 FTE.

Key Responsibilities:

• Lead site monitoring activities for ophthalmology trials, ensuring adherence to protocol, GCP, and regulatory requirements.
• Implement risk-based approaches to ensure proactive issue resolution and maintain trial quality.
• Manage ethics committee submissions, amendments, and periodic regulatory reporting, including safety event notifications.
• Contribute to site activation, including Site Initiation Visits (SIVs) and investigator training.
• Ensure proper trial documentation, monitor data integrity, and support study closeout.

Qualifications:

• Prior experience in clinical trial monitoring within a CRO, biotech, or pharmaceutical company.
• At least 1 year of therapeutic expertise in ophthalmology trials.
• Experience in retinal disorders.
• Gene therapy experience is a plus but not required.
• Familiarity with local and international regulatory requirements.
• Strong interpersonal skills to engage effectively with sponsors and site staff.

Join us in driving forward cutting-edge clinical research in ophthalmology and beyond.

A Bit More About Us

Our journey began over 27 years ago in Sweden, in the city of Lund. As a full-service, global Contract Research Organization (CRO), we build solution-driven teams working towards a healthier future. Bringing together over 800 professionals, TFS delivers tailored clinical research services in more than 40 countries with flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology, and Ophthalmology.

Our core values of Trust, Quality, Passion, Flexibility, and Sustainability are our guiding light serving as the framework for decision-making at all levels of the organization. They assist us in attracting and retaining valuable talent who share our sentiments, resulting in high employee engagement and satisfaction. By aligning on these fundamental values, we cultivate a unified force, geared towards innovation and excellence. This collective effort propels us towards our shared goal and fosters a culture of mutual respect and collaboration. Together we make a difference.