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Job Details

Senior Clinical Project Administrator in Czech Republic!

Company: Covance
Location: Czech Republic
Reference: 63605BR
Closing Date: 21 Dec 16
Type: Permanent
Salary (£): Competitive
Benefits:

Job Summary:

You can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in Covance's impressive history of company stability and growth. We've achieved these results by fostering a work environment that encourages, develops and leverages our team's capabilities.

Requirements:

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. 

This is your chance to become part of a team that helps to bring miracle of medicine to market sooner. 

We are currently seeking a pro-active, driven Senior Clinical Project Administrator to join our expanding team. 

Responsibilities / Duties: 

  • Train and mentor Clinical Project Administrators 
  • Provide clerical support to project team (e.g., word processing, proofreading and editing correspondence, large and small documents, mailings, shipment of study files, fax and photocopy documents, assemble study documents, and arrange meetings, etc.) 
  • Set up and maintain clinical investigator files and documentation 
  • Prepare study-related documents and other materials for delivery to archives, at appropriate intervals 
  • Prepare investigator budget payments and tracking systems; generate tracking reports as assigned 
  • Prepare monitoring visit documentation for Clinical Research Assistants and above, as requested by supervisor 
  • Data entry and maintenance of selected study tracking data 
  • Assist with coordinating vendors 
  • Organize/prepare for client meetings/teleconferences 
  • Assist/prepare for client or internal audits 
  • Provide telephone coverage and related support duties 
  • Perform other administrative duties as assigned by management 


Education / Qualifications: 

  • min 2 years experience in clinical trial field (previous Clinical Monitoring Assistant or similar experience) 
  • very good PC systems skills (excel, world, power point) plus CTMS 
  • fluent English both spoken and written 
  • Czech native 
  • excellent organizational and communication skills 
  • knowledge of CT local regulation and GCP 


THERE IS NO BETTER TIME TO JOIN US!

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

Apply for this job: Senior Clinical Project Administrator in Czech Republic!

Contact Information:

Address:  Covance- Warsaw


Poland
Tel: 
Fax: 
Website:  Visit Our Web Site

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