Clinical Project Associate

Highly Competitive Salary
  1. Permanent
  2. Clinical Trial Assistant (CTA), Clinical Research Associate (CRA), Project/Study Manager (CSM/CPM)
  3. United States
Redwood City, USA
Posting date: 13 Aug 2020
CR.CN.31257

Proclinical is currently recruiting for a Clinical Project Associate with a biotechnology company located in Redwood City, CA.

Job Responsibilities:

  • Work under general supervision for routine tasks and with detailed instructions on new assignments.
  • Tracking and preparing study-specific information utilizing databases, spreadsheets, and other tools.
  • Assists with management of the electronic trial master file.
  • Under close supervision reviews and participates in the quality assurance of data or documents.
  • Arranges meeting logistics.
  • Drafts meeting agendas and assists in preparing meeting minutes.
  • Interacts with other departments, as directed, to complete assigned tasks.
  • Travel may be required.
  • Excellent verbal and written communication skills and interpersonal skills are required.
  • Must be familiar with Word, PowerPoint, and Excel. Knowledge of FDA and or EMEA Regulations, ICH Guidelines, GCPs, and/or familiarity with standard clinical operating procedures is a plus.
  • Must be able to work both independently and as part of a team.

Skills and Requirements:

  • Past clinical experience and must be familiar with Good Clinical Practices (GCPs) and ICH guidelines

If you are having difficulty in applying or if you have any questions, please contact Catherine Nguyen at 215-531-5643.

ProClinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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