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Job Details

Clinical Research Associate

Company: CROMSOURCE
Location: Poland
Reference: HQ00001048
Closing Date: 15 Nov 17
Type: Permanent
Salary (£): On Application
Benefits: Excellent and Comprehensive Benefits – see below

Job Summary:

(Senior) Clinical Research Associate - oncology   TalentSource Life Sciences is currently searching for an experienced Clinical Research Associate (CRA) for our customer, one of top 20 pharmaceutical companies. We are looking for reliable candidates with strong site management skills and the ability to work independently as it's a home based opportunity. The successful candidate will be working on studies dedicated to one client. Freelance contract is possible.

Requirements:

(Senior) Clinical Research Associate - oncology

TalentSource Life Sciences is currently searching for an experienced Clinical Research Associate (CRA) for our customer, one of top 20 pharmaceutical companies.

We are looking for reliable candidates with strong site management skills and the ability to work independently as it's a home based opportunity. The successful candidate will be working on studies dedicated to one client. Freelance contract is possible.

Responsibilities:

  • Perform feasibility analysis;
  • Preparation/submission/follow up of Regulatory approval process;
  • Contract negotiation with Investigator site;
  • Interface with the project management team to ensure that each clinical study site can or will achieve optimal outcome as defined by the Sponsor;
  • Conduct all pre-trial activities, including pre-study visits;
  • Conduct on-site study initiation visits, interim monitoring visits and study closure visits;
  • Monitoring the study status and the correctness of study conduct, especially compliance with the study protocol and ICH GCP guidelines by direct meetings with investigators and other people engaged in the study. Monitoring will be performed in accordance with the Study Protocol;
  • Review and collect (e)CRFs;
  • Perform drug or device accountability;
  • Complete Monitoring Visit Reports;
  • Administration of the clinical trial, collection of required critical documents, checking and archiving study files;
  • Timely distribution of queries to investigators and executing answers;
  • Report incoming SAEs and follow-up of activities connected to SAEs reporting;

Work Experience:

  • Min 2-3 years of the relevant CRA experience
  • Oncology experience will be additional advantage

Education:

  • Educated to degree level (biological sciences, pharmacy or other health related discipline preferred).

Language Skills:

  • Advanced English
Oncology, Clinical Research Associate, Monitor

Apply for this job: Clinical Research Associate

Contact Information:

Address:  UK Office
CROMSOURCE Suite 3 Lomond Court Castle Business Park Stirling United Kingdom
FK9 4TU
Scotland
Tel:  +44 (0) 1786 468990
Website:  Visit Our Web Site

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