ClinForce is currently seeking a Senior Clinical Research Associate - CRA for Durham, NC.
Successful candidate will manage study process to ensure adherence to protocol, SOPs, GCP/ICH Guidelines, applicable regulatory requirements and other documentation requirements. Candidate will monitor vendors and other service providers for quality of service as well as initiate and maintain expedited identification, retrieval and review of study documents particularly those required for site activation/study start-up. In addition, candidate will develop ICF templates and review study specific ICF(s), participate in CRF development and completion guidelines and review templates and plans developed by CRO.
Experience/Minimum Requirements: 10+ years experience in Clinical Research including site monitoring experience; Most recent experience must be working in-house for a pharmaceutical company
Education/Degree: BA/BS preferred
Interested candidates should send resumes to response@clinforce.com or fax to 866-941-1400 with 'CF3022 MON' in the subject line.
