In-house CRA - South of England
- Employer
- Labcorp
- Location
- London, United Kingdom
- Salary
- Competitive
- Start date
- 7 Jan 2022
- Closing date
- 24 Jan 2022
View more
- Discipline
- Clinical Research, Clinical Operations
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Get ready to redefine what's possible and discover your extraordinary potential at Labcorp. Here, you'll have the opportunity to personally advance health-care and make a difference in peoples' lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you'll be empowered to own your career journey with mentoring, training and personalized development planning.
Join us as we speed the delivery of ground-breaking therapies and anticipate tomorrow's drug development challenges, creating new possibilities for our clients-and your career.
LabCorp is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. We have an exciting opportunity available to join our team.
We are looking to recruitIn House Clinical Research Associate to join our team in UK - full time, permanent, office based Maidenhead.We are looking for someone with an interest in the industry to join our team and start their clinical career!
As an essential member of the Project Team, the IHCRAs are responsible for supporting the execution of clinical trials. IHCRAs work closely with their CRA colleagues to maintain quality and deliver study milestones in the UK and Ireland.
General Responsibilities in the role include:
- Monitoring site performance and creating action plans for sites not meeting expectations, in conjunction with the site CRA
- Assist CRAs with the preparation for site visits (running reports, QC of files, resolving action items from previous visits)
- To liaise with the project team and others to distribute and track clinical trial supplies to ensure sites have enough to continue recruitment
- Perform Case Report Form review, query generation and resolution, assisting sites as needed
- Document review and collection to ensure compliance and inspection readiness of TMF
- Tracking and processing invoices from investigator sites against agreed contracts and budgets
- Undertake project related administrative tasks (meeting minutes, recruitment tracking, site document preparation)
IHCRA may also be required to attend onsite monitoring visits as a co-monitor with experienced CRAs to assist with tasks such as site regulatory file review and drug accountability.
Education/Qualifications:
- University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
Experience:
- Preferred candidates will have completed a year in industry during University studies or have relevant work experience in the clinical trial industry or related field (medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing)
Company
At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.
- Website
- https://careers.labcorp.com/global/en
- Location
-
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom
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