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Job Details


Company: Covance
Location: Prague, Czech Republic
Reference: 38070BR
Closing Date: 09 Feb 17
Type: Permanent
Salary (£): Competitive

Job Summary:

Covance is one of the world's most dynamic drug development services companies, providing integrated, tailored solutions to the pharmaceutical and biotechnological industries. This is your chance to become part of a team that helps to bring miracle of medicine to market sooner.


At the moment we are looking for Clinical Research Assistants!

Your responsibilities will include assisting Clinical Research Associates (CRAs) and project team members with site tasks (e.g. review of Case Report Forms and Study File Notebook, drug accountability) other administrative activities as required (e.g. payments to investigators, correspondence with clients, preparation of status reports, and organization of investigators' meetings)


  • Provide clinical support for projects according to Standard Operating Procedures, ICH Guidelines and GCP
  • Act as contact for project team and study sites
  • Assist with generation and reconciliation of queries to investigative sites/clients to resolve problem data.
  • Assist with the management of study supplies and organize shipments
  • Create, update, track, and maintain study-specific trial management files, tools, and systems
  • Co-ordinate meetings with clients, investigators, and project team, including taking minutes
  • Ensure compliance with S.O.P.s, FDA, ICH, and GCP regulations for clinical conduct in all aspects of daily work
  • Provide input in writing Monitoring Conventions as assigned
  • Assist in submissions and notifications to Ethics Committees and Regulatory Authorities.

Required skills, experience and education:

  • Previous Experience in a corporate environment; Experience within clinical research preferred;
  • Diploma – Secondary Education or equivalent;
  • Understanding of the clinical trial process;
  • Good oral and written communication skills
  • Ability to set priorities and handle multiple tasks simultaneously
  • Good organizational and time management skills.
  • Computer literacy (word processing and spreadsheet software).
  • Aptitude for handling and reviewing numerical data.
  • Ability to operate standard office equipment (e.g., fax, copier).
  • Fluency in local and English language.

In return, we offer you the opportunity to develop your career with an international organization; to pursue further training and to take advantage of our flexible conditions and attractive remuneration package.

Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us.

Apply for this job: CLINICAL RESEARCH ASSISTANTS / Prague, Czech Republic

Contact Information:

Address:  Covance- Warsaw

Website:  Visit Our Web Site

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