Full-Time Clinical Research Associate

C3 Research Associates is a Seattle based clinical research organization providing full service management for biomedical and pharmaceutical clinical trials. We specialize in supporting small and mid-sized companies through the entire clinical trial process. We are a nimble organization that is dedicated to encouraging innovation.

C3 Research Associates is currently seeking a full-time Clinical Research Associate to join our virtual team based in the Puget Sound area. This position will coordinate research and administrative strategies for the management of clinical research.

Primary Responsibilities:

• Lead study start-up activities including the review of clinical and project-related documents
• Act as site liaison to CRAs/Project Managers
• Primary contact for sites, Project Managers, Clinical Data Managers, contract Clinical Research Associates, and other staff for project-related inquiries and issues
• Participate regularly in project calls and provide updates on study
• Manage and track study progress on recruitment/site selection, site readiness, IRB/EC submissions, patient enrollment, etc.
• Ability to prepare appropriate, timely and accurate communication to internal and external teams, consultants and investigative site personnel.
• Conduct on-site visits (Qualification, Initiation, Interim, Close-Out) to monitor study progress and assure compliance with protocol-requirements and applicable regulations and ICH/GCP
• May include participation in financial budget management , bid defense meetings, and formulating strategic solutions to ensure study success

Qualifications:

• Minimum of 3 years of related clinical research experience
• Previous experience in a small or start-up company with a remote work environment is desirable.
• Bachelor’s degree in a life science or medical discipline, or equivalent applicable experience, is preferred.
• Ability to travel up to 50%, based on project needs.
• Proficiency with Microsoft Office Suite, electronic data systems, and other database programs is required.
• Must have the ability to work independently and maintain confidentiality.
• Excellent oral and written communication skills and the ability to communicate effectively with all levels. This position requires the ability to work with outside agencies in a professional manner.
• Attention to detail and accuracy is essential.
• A working knowledge of GCP and other regulatory requirements

If you are an energetic and bright individual we want to hear from you! Please submit your resume to: careers@c3-research.com.