Top Three Skills: Study management, vendor management, investigator meeting. Must meet following requirements - Drafts and coordinates review of relevant documents including protocols, informed consents, case report forms, monitoring plans, investigator brochures and clinical study reports - Must be able to understand, interpret and explain protocol requirements to others - Maintains study timelines - Coordinates review of data listings and preparation of interim/final clinical study reports - Assists in determining the activities to support a project's priorities within functional area - Contributes to development of RFPs and participates in selection of CROs/vendors - May be asked to train CROs, vendors, investigators and study coordinators on study requirements - Contributes to development of study budget -May serve as a resource for others within the company for clinical trials management expertise - Able to examine functional issues from an organizational perspective - Participates in the recruiting and hiring process for CPAs and CTMAs and support their professional development - May contribute to development of abstracts, presentations and manuscripts - Under supervision, may design scientific communications within the company Must be able to participate in multiple departmental or interdepartmental strategic initiatives under limited supervision - Must have a general, functional expertise to support SOP development and implementation About Aerotek: Aerotek, headquartered in Hanover, Md., is a leading provider of technical, professional and industrial staffing services. Established in 1983, Aerotek is an operating company of Allegis Group, the largest provider of staffing services in the U.S. Aerotek operates a network of more than 200 non-franchised offices throughout the U.S., Canada and Europe. For more information, visit aerotek.com. Aerotek is acting as an Employment Agency in relation to this vacancy. ()
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