CRA II / Senior CRA - Sweden

Created by: Covance
Added: 25.03.2020

Advert description

Job Overview

Covance is searching for a CRA II or Senior CRA in Sweden to monitor trials mainly within Oncology and Cardiology diseases.

This role is 100% SPONSOR dedicated with a prestigeous Pharmaceutical company so there will be no working across multiple SOPs!!

What makes this opportunity special?
  • Career progression will be exceptional because there are lots of studies coming through in 2019 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-based OR 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
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
Experience:
  • 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.

Covance is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

Specific details

Type of Contract Full time
Preferred Education Bachelor's
Level of Experience 2-5 years

Location

Sweden, Europe
Stockholm