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Clinical Research Coordinator
- Permanent
- CRA Manager, Project/Study Manager (CSM/CPM), Program Manager / Director
- United States
This vacancy has now expired. Please see similar roles below...
Proclinical is currently recruiting for a Clinical Research Coordinator with a pharmaceutical company located in San Mateo, CA. A successful candidate will have past clinical experience and must be familiar with Good Clinical Practices (GCPs) and ICH guidelines.
Job Responsibilities:
- Tracking and preparing study-specific information utilizing databases, spreadsheets, and other tools.
- Processes drug shipments, drug returns, and assists with in-house drug reconciliation.
- Orders and maintains inventory of clinical supplies.
- Orders and ships case report forms.
- Assists with development of documents for site binders
- Assembles and prepares distribution of site binders.
- Serves as CRA back up providing verbal and written communication with study personnel.
- 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.)
- May assist with monitoring visits under the direct supervision of senior staff.
Skills and Requirements:
- 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 familiarity with standard clinical operating procedures.
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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