CRA II - Denmark
- Employer
- Labcorp
- Location
- Copenhagen, Denmark
- Salary
- Competitive
- Start date
- 19 Oct 2021
- Closing date
- 12 Nov 2021
View more
- Discipline
- Clinical Research, Clinical Research Associate
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
Labcorp Drug Development is looking for a CRA II to be client dedicated with a top 10 pharmaceutical company in Denmark. To apply you must be looking for a full time position and be based relatively close to Copenhagen.
We can offer a permanemt contract and candidates can be 100% home based. Therapeutic areas include Oncology, Diabetes, cardio and rare diseases. Monitoring frequency will be approximately 6 visits per month.
Job Summary
- Performs/participates in study site selection visits in the investigational sites
- Performs Primary CRA function for eCRF studies during the set-up phase
- Prepares/collects all study site essential documents needed prior to study initiation in collaboration with the Clinical Project Assistant (CPA) and Start-Up/Regulatory Team
- Facilitates negotiation of site Clinical Trial Agreements (CTA) prepared by the Regional/Local Clinical Project leader (RCPL) or Start-Up/Regulatory Team
- Ensures that sites apply for and receive hospital/practice/institution approval (e.g. R&D).
- Organises/participates in study initiation meetings in which are provided scientific and technical knowledge concerning the study procedures and its organisation
- Works with RCPL, Lead CRA and CPA to prepare, organise and participate in investigator meetings.
- Assists the RCPL/CPA in maintaining and ensuring the completeness of the local study files, checking the country-level (when Lead CRA for studies with regional CPL) and centre-specific files at regular intervals and reconciling with the investigator study files
To apply for this position please email your CV to andy.smith @covance.com or for a confidential discussion please call Andy Smith on + 44 (0)7775 848 250
REMOTE
Education/Qualifications:
Appropriate education (life science degree / nursing qualification)
Experience:
Candidates must be an experienced CRA with at least 1 years' monitoring experience
Knowledge of and experience with GCP and other regulations in force; ability to learn and apply SOPs
Good IT skills in, e.g. MS Office, are essential, for planning, tracking, communicating and reporting
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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