Clinical Research Specialist

Clinical Research SpecialistDuration: 12 Months+ Contract (possibility of extension)Top 3 qualifications: • Previous clinical research experience • Ability to prioritize and strong critical thinking skills • Attention to detail and strong communication skillsResponsibilities: Assist with overall successful conduct of assigned clinical studies consistent with applicable regulations, guidelines, and policies.Assist in preparation of study materials and/or training. Interface with, and assure training of investigators, site staff, and client clinical staff.Assist in site initiation (e.g. start-up document preparation, distribution, receipt, and review).May arrange conference calls, staff meetings and training events.Assist data management group with review of clinical data/information and oversight of data correction.May assist with oversight of activities performed by Contract Research Organizations (e.g. CROs, core labs).Able to refer to Standard Operating Procedures (SOPs) and Department Operating Procedures (DOPs) for guidance on everyday study tasks.Contribute to ongoing SOP development and review. Participate in training to enhance knowledge base.Must be willing to assist with other duties as needed such as filing and document tracking.Qualifications: Must have ability to prioritize and critical thinking skills and previous clinical research experience. Must have strong written, oral, and interpersonal communication skills and high attention to detail and accuracy. 3-5 years of experience Education required: 4 year degree