Clinical Research Coordinator

Assists Clinical Management and CRAs to initiate, conduct, and complete Phase I-IV clinical trials, as well as assist with other related clinical activities.
Interacts as directed with clinical investigators, study site staff, and other Dynavax departments to meet overall project and department objectives.
Organizes, files, and maintains clinical documents in compliance with Good Clinical Practice and Dynavax’s policies and procedures.
Assists with the production and/or distribution of study-related information and materials for study sites, vendors, institutional review boards, and consultants.
Assembles documents and supplies as needed to support CRA monitoring visits.
Assists in tracking status of critical study documents and study site payments.
May assist in reviewing clinical documents for completeness.
Assists in the planning, preparation and coordination of internal and external presentations and meetings as needed.
Processes and submits clinical documents for permanent storage as needed.
Helps ensure that clinical documents are available for review and audit by quality assurance groups and regulatory agencies.

ASG, Inc. is a nationwide contract consulting and contingency recruiting firm. Our reputation for excellent service, our knowledge of the market place, and our success in the recruiting industry make it possible for us to provide complete and comprehensive contract consulting and contingency technical services. Align yourself with ASG and get: challenging assignments and competitive compensation (with or without benefits). Our job is to keep you focused on your work and to provide you with a comfortable working relationship with us, your business partner, ASG.
REQUIREMENTS
Direct clinical research experience is not a requirement; however, knowledge of clinical research or experience in a related field with a college degree (AA, BA, or BS degree) is desirable.
Must be detail-oriented and have excellent organizational skills.
Must be able to multitask.
Must be able to work effectively in project teams as well as operate with independence on general routine assignments.
Must have good written and verbal communication skills.
Must have good computer skills, preferably in a Microsoft Office environment (Word, Excel, and PowerPoint).
Must be able to communicate effectively with members of other departments and with study site personnel (physicians, study coordinators, nurses, etc.) as needed.

If you would like to be considered for this position, please forward your resume to [Click here for email] please reference the job title and number.