Clinical Data Specialist

Covance Inc Located in: Raleigh,  North Carolina
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Covance Inc Biotechnology Jobs Pharmaceutical Careers
 

JOB DESCRIPTION

Specific responsibilities of the Clinical Specialist include:

  • Development and entry of Specimen Test Plans (STP)
  • Codification of Informed Consents based on company SOP’s
  • Assist in preparation of annual update of global Regulation and Guidance documents
  • Perform Enhanced Monitoring functions
  • Assist with the development and maintenance of training documents for clients in sync with new system releases
  • Assist Quality Assurance in regulatory certifications (ISO, Data Privacy, etc), validation processes, and SOP writing

 

  • A Bachelor’s degree, preferably in science or a related field
  • At least 3 years of experience working in clinical trials, laboratory, or specimen management
  • Proven ability to plan, prioritize, and manage in a fast-paced environment with a high degree of initiative
  • Strong drive for process optimization and data integrity
  • Excellent communication and interpersonal skills with great attention to detail
  • Experience in molecular biology, Clinical Pharmacogenomics or biomarker research is highly preferred
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CRITICAL REQUIREMENTS

COMPANY INFORMATION

Covance Inc. is proud to be the only drug development company with a full range of research and development services—from lead optimization, to commercialization and life cycle management. Covance, headquartered in Princeton, NJ, is the drug development business of LabCorp with global operations in more than 30 countries.

JOB INFORMATION

Seniority Level:
Experienced - Not Management
Function:
  Clinical Research / Affairs
Preferred Industry Background:
 
Managing a team of:
N/A
Required Travel:

Base Salary:
Confidential
Bonus:
Benefits:
Other Compensation: