Senior CRA- Office Based with Minimal Travel!

Senior CRA- Office based with minimal travel! Client DescriptionWe are currently partnering with a Biotechnology company in the greater Seattle area. This company is focused on expanding their clinical division and seeking an experienced Senior CRA for an office based position.  Benefits Competitive salary 401k plus matching program Stimulating environment where employees thrive in an atmosphere that promotes individual achievement and teamwork Established training program Excellent benefits package includes medical, dental, and vision,  Short Term Disability, Basic Life Insurance, Supplemental Life Insurance and Long Term Disability available, Long Term Care, Flex Spending Accounts, Employee Assistance Program, Employee Stock Purchase Plan Requirements:· Bachelor’s in scientific discipline or relevant medical training, RN, or health care· Minimum of 5 years pharmaceutical clinical development experience or equivalent· Experience with CRO management· Strong understanding of GCP and regulatory issues· Ability to travel approximately 20%· Function as a liaison between senior management and third party vendors.· Exceptional communication (oral and written) and organizational skills · Strong multi-tasker and excellent problem solving skills· Strong leadership skills· Oncology /Hematology clinical trial experience is preferred. Principal Duties and Responsibilities:Coordination of all clinical operations and monitoring activities that are essential to initiate, monitor, and complete clinical programs at the clinical trial site level. Responsibilities include but are not limited to:· Providing support to other CRAs and assisting in the initiating, monitoring and coordinating day-to-day operations of investigational clinical trial sites as needed· Providing the clinical operation input to the clinical project team· Participating in the evaluation, training, and refining of departmental SOPs and guidelines, and developing standard reports, templates and forms· Training, mentoring, and possibly managing CRAs and CTAs in clinical trial management· Overseeing investigational drug supply chain and accountability system, including projection of needs, requisition process and accountability activities· Providing operational/ clinical trial site monitoring input to the essential study documents including the protocol, informed consent, CRF’s, Statistical Analysis Plan, and Clinical Study Report as assigned  Please include the position title in the subject line of your email to ensure immediate consideration and forward your resume/CV (Word format) to stacey.sears@wilmingtongroup.com      MRINetwork, one of the world's largest search and recruitment organizations, has over 1,000 offices in more than 35 countries. Each office is a single point of contact that allows candidates to access high-quality positions virtually anywhere in the world. MRINetwork recruiters are industry specialists who typically have real-world experience in the industries they serve. LOCATION: Seattle, WA 98101 JOB CATEGORY: Biotech/R&D/Science TYPE: Full Time, Employee JOB REFCODE: Eb-1914213640 COMPANY: The Wilmington Group CONTACT NAME: Stacey Sears EMAIL: Apply by Email