CRA II / Senior CRA - Sweden
- Employer
- Labcorp
- Location
- Stockholm, Sweden
- Salary
- Competitive
- Start date
- 12 Jan 2022
- Closing date
- 1 Feb 2022
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 searching for a CRA II or Senior CRAin Sweden to monitor trials mainly withinOncology and Cardiology diseases.
This role is 100% SPONSOR dedicated with a prestigeous Pharmaceutical company so there willbe no working across multiple SOPs!!
What makes this opportunity special?
- Career progression will be exceptional because there are lots of studies coming through in 2021 across a variety of therapeutic areas
- We offer lots of flexibility with great opportunity to progress into a variety of areas such as Project Manager, CTL, Line Manager, SSU Manager and cross boarder roles in the future.
- The working conditions within our Swedish team is great! A very positive environment where everyone works together well and in harmony.
- The job is permanent, full time & 100% home-basedOR office based in Stockholm.
- You will be joining a large team with a well organised structure and robust processes in place
- Competitive salary, car allowance and benefits package, including lunch vouchers
- There will be no formal contractual expectations regarding frequency of visits
REMOTE
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)
- In lieu of the above requirement, candidates with three (3) or more years of relevant clinical research experience in pharmaceutical or CRO industries may be considered
- Fluent in Swedish and English
- Minimum of two (2) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits).
- In lieu of the above requirements, candidates with > five (5) years supervisory experience in a health care setting and three (3) years clinical research experience in the pharmaceutical or CRO industries (including monitoring) will be considered.
- Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.
- Excellent site monitoring skills.
- Excellent study site management skills.
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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