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Job Details

Senior Clinical Research Associate

Company: United BioSource Corporation.
Location: London, United Kingdom
Reference: REQ20005336
Closing Date: 08 Dec 16
Type: Full Time
Salary (£): Competitive
Benefits: Comprehensive Package

Job Summary:

Consistently completes site monitoring reports, confirmation/follow-up letters per UBC and/or client SOPs; signs, scans and/or provides to CSS/RDS for filing in Trial Master File according to UBC and/or sponsor timelines requiring minimal correctionsConsistently completes on site monitoring in accordance with project specific timelinesEnters site visits, confirmation/follow-up letters and site monitoring reports into CTMSAttends project team meetings, department meetings and minimum of...

Requirements:

Since 2003, UBC has been the home for people who are passionate about innovation, service and making a difference in peoples' lives and in the healthcare and biotech industries. As a service organization, UBC employees are our greatest resources. Their skills and expertise are what sets us apart in the industry.

Working here, you will support the development of life-changing therapies. You will work with peers who will become friends and leaders who listen to your feedback in a collaborative, innovative and fast-paced culture. You will enjoy competitive benefits, pay-for-performance compensation and rewarding recognition that promotes internal quality and critical alignment of our business objectives. And finally, you will enjoy the vast network of resources of our Fortune 20 parent organization, Express Scripts.


Brief Description:  
The Senior Clinical Research Associate (SCRA) is responsible for monitoring in accordance with ICH, GCP, CFR guidelines, UBC and project SOPs.
 
Specific Job Duties:


  • Consistently completes site monitoring reports, confirmation/follow-up letters per UBC and/or client SOPs; signs, scans and/or provides to CSS/RDS for filing in Trial Master File according to UBC and/or sponsor timelines requiring minimal corrections
  • Consistently completes on site monitoring in accordance with project specific timelines
  • Enters site visits, confirmation/follow-up letters and site monitoring reports into CTMS
  • Attends project team meetings, department meetings and minimum of monthly 1:1 with manager; responsible for content of these meetings
  • Completes Regulatory Binder and Investigational Product reconciliation
  • Maintains regular contact with assigned sites per study requirements
  • Consistently completes sponsor specific training and documentation within requested timelines
  • Ensures follow-up of site issues and action items per UBC/sponsor timelines
  • Ensures completion of Call Log or Telephone Contact Report detailing communication with sites per protocol

 
Requirements:


  • Bachelor’s degree required
  • Minimum of  24 months active monitoring experience
  • Thorough knowledge of medical terminology
  • Good written and verbal communication skills
  • Ability to perform tasks in CTMS, EDC, Outlook and client specific systems (if applicable)
  • Thorough knowledge of ICH, GCP, CFR and SOPs
  • Up to 50% travel



*LI-AF1-UBC

 


NO AGENCIES PLEASE

Apply for this job: Senior Clinical Research Associate

Contact Information:

Address:  United BioSource Corporation (UBC)
Europe Headquarters
26-28 Hammersmith Grove
London
United Kingdom
W6 7HA
England
Tel:  +44 (0)20 8834 0100
Website:  Visit Our Web Site

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