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Job Details

SCRA/CRA II (Oncology experience) - Stockholm, Sweden

Company: Covance
Location: Stockholm
Reference: 15599
Closing Date: 27 Apr 18
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

This is a CRA position available to work within our Phase II-IV CoSource division directly with pharmaceutical company. As an experienced CRA you’ll be involved in initiation, routine & close out visits concentrating on sites in Sweden.

Requirements:

Clinical Research Associates with Oncology Experiance – SWEDEN 

We are currently looking for talented Clinical Research Associates (3 vacancies opened!) to work for us in the Co-source department as our sponsor, a well-known pharma company, is currently expanding their Clinical Operations team.  This are a full-time, permanent and home-based positions in Sweden.


Requirements:

  • Ability to monitor Clinical study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
  • Excellent understanding of Serious Adverse Event reporting
  • Previous clinical research monitoring Experience (about 3 years) (including pre-study, initiation, routine monitoring and closeout visits) in Sweden
  • Oncology experiance required
  • Fluency in both English and Swedish
  • Knowledge in the TA oncology - experience in additional TAs also favorable
  • Proven skills in site management including site performance and patient recruitment
  • Skills in building relationship with customer
  • Flexible in travelling (2-3 days/week)
  • Service minded
  • Team player
  • IT oriented 


Duty Highlights:

  • As a SCRA you will manage all aspects of study site monitoring according to SOPs, GCP, and ICH guidelines, including pre-study qualification and initiation visits, routine monitoring, close-out of clinical sites, and maintenance of study files.

 

Responsibilities include:

  • All aspects of site management as prescribed in the project plans
  • Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks
  • Negotiation of study budgets with potential investigators and collaboration with Covance legal department with statements of agreements
  • Serious Adverse Event (SAE) reporting, production of reports, narratives and follow up of SAEs.
  • Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Covance or client data management systems

 

Why Covance?
At Covance, you will join like-minded professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world.

 

We welcome your application and believe this decision may be the most rewarding career move you will ever make!

Apply for this job: SCRA/CRA II (Oncology experience) - Stockholm, Sweden

Contact Information:

Address:  Covance- Warsaw


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