Clinical Research Associate - Freelance - 0.1FTE at TFS HealthScience

London, England, United Kingdom -

Full Time

Start Date

Immediate

Expiry Date

23 Aug, 26

Salary

0.0

Posted On

25 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Site Monitoring, GCP, Clinical Trial Processes, Source Data Verification, TMF Review, Regulatory Compliance, Clinical Research, Site Oversight

Industry

Pharmaceutical Manufacturing

Description

About this role TFS HealthScience is a leading global mid size Contract Research Organization CRO that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service capabilities, resourcing and Functional Service FSP solutions. The Clinical Research Associate CRA is responsible for supporting clinical trial activities at a single site in London, ensuring that the study is conducted in accordance with protocol, GCP and regulatory requirements. This is a part time role with limited site oversight. As part of our SRS FSP team, you will be dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area. Key Responsibilities Perform site monitoring visits as required for one site in London Ensure compliance with study protocol, GCP and applicable regulatory requirements Act as the main point of contact for site staff Support site documentation review including TMF and essential documents Perform source data verification and ensure data quality Collaborate with the wider study team to support smooth study execution Qualifications Previous experience as a CRA with independent monitoring responsibilities Strong knowledge of GCP and clinical trial processes Experience with on site monitoring activities Ability to work part time on a 0.1 FTE basis Based in or able to travel to London What We Offer We provide opportunities for personal and professional growth in a rewarding environment. You will join a team that values collaboration, quality and making a difference in the lives of patients. Our core values of Trust, Quality, Passion, Flexibility and Sustainability guide our decisions and shape our culture. By aligning on these values, we foster collaboration, innovation and a shared commitment to excellence. Together, we make a difference. A Bit More About Us Our journey began over 30 years ago in Sweden, in the city of Lund. As a full service global CRO, we build solution driven teams working toward a healthier future. Bringing together over 600 professionals, TFS delivers tailored clinical research services in more than 50 countries, offering flexible clinical development and strategic resourcing solutions across key therapeutic areas including Dermatology, Neuroscience, Oncology and Ophthalmology.

Responsibilities

The CRA is responsible for supporting clinical trial activities at a single site in London, ensuring compliance with protocol and GCP. Key tasks include performing monitoring visits, reviewing site documentation, and conducting source data verification.