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CRA II / Senior CRA - Sweden

Covance 4/16/2019 6:17:59 PM
JOB ID: 22115 Category: Clinical Research Associates
Regional, Sweden



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


* 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.

Position Type: Full-Time

Location: Regional, SWE - Sweden


Covance Recruiting Process

Below is a general Overview of Our Recruiting Process

If you’d like to work for us, please submit your resume/CV online. If your ability to use or access our electronic application is limited due to a disability, please visit or call 1-800-978-4473 for help.

We consider applications from everyone who is interested in a position with us and who meets the required criteria and qualifications.

If your application is selected, someone from our recruiting team will contact you to arrange an initial screen. We may carry this out over the phone or at a face-to-face meeting. You must complete the screen to be considered for the position.

Based on the results of the initial screen, we may invite you to an interview. One of our recruiting team members will contact you to arrange this. The process may involve several interviews, initially over the phone, and then face-to-face with different members of the hiring team.

Our interviews follow a behavioral-based format. This means we’ll ask you to give us information that’s specific to your professional and educational experiences.

Hiring team members will share and discuss their input and then make their decision.

If you’re the person who best meets the requirements of the position, a member of the hiring team will get in touch to make you an offer of employment. Covance is an eVerify employer (United States only).