Skip to main content

This job has expired

Sr Clin Res Assoc I

Employer
Labcorp
Location
Zollikon, Switzerland
Salary
Competitive
Start date
15 Nov 2019
Closing date
20 Nov 2019

View more

Job Details

Covance is looking to hire a SCRA with Oncology experience in Switzerland.


  • You would be employed permanently by Covance on a competitive salary and outsourced to a pharmaceutical company - 100% dedicated to their portfolio (mainly ONCOLOGY) across Phase 2 and Phase 3.
  • This opportunity sits within our FSP business model - a very attractive environment with great potential for career development.
  • Outsourced to a top ten pharma company, you will primarily be monitoring clinical trials across the main centres in Switzerland within the Oncology therapy area - phase II and III
  • Dedicated to our Client (one Sponsor) 100% of the time, you will be well supported by a dedicated Covance line manager as well as by the Client project teams.
  • Our strategic relationship with our pharma client also enables a focus on training, pastoral care and career development opportunities within this model. Work life balance is also of utmost importance within this partnership.
  • The primary responsibilities of this position is to conduct routine site monitoring visits and participate in site selection, site initiation and study closure activities. This person will ensure that the clinical trial is being conducted according to the approved protocol, amendments and in compliance with Good Clinical Practice (GCP), Company SOPs, and all applicable regulatory requirements
  • Ideally we would like the CRA to have at least 18-24 months independent monitoring experience.



Please call Olga Zhikhareva on 0049 89 20 30 43 717 for further information OR you can send your CV and application direct to Olga at olga.zhikhareva@covance.com


Education/Qualifications:
  • Position requires Bachelor or nurse degree, preferably in the Life Sciences
Experience:
  • Minimum of 2+ years of experience in the pharmaceutical / biotechnology industry or CRO as a Clinical Research Associate from study start-up to database lock.
  • Strong Oncology monitoring experience in phase 1-3 pharmaceutical/ biotechnology clinical trials
  • Possess good understanding of ICH guidelines, Good Clinical Practices (GCP), clinical research ethics, patient privacy laws, and other relevant, country regulatory requirements
  • Good knowledge of concepts of clinical research and drug development
  • Strong working knowledge of Electronic Data Capture, Interactive Voice/Web Response System and Clinical Trial Management System
  • Ability to handle and prioritize multiple studies and projects
  • Ability to work effectively in a team/matrix environment
  • Ability to understand technical, scientific and medical information
  • Demonstrated strengths in planning, organizational, project management, analytical skills, oral and written communication, time management, conflict management, problem solving, attention to detail, and interpersonal skills
  • Fluent in English, German and French or Italian
  • Ability to travel 60%
  • Independent site management experience in a German speaking country is essential for this role.

Locations:
Zollikon, Switzerland

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.

 

 

 

 

Company info
Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert