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Job Details

Clinical Research Coordinator

Company name
Asthma & Allergy Center

Bellevue, NE

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We are looking for a highly motivated, responsible individual to coordinate clinical research trials dealing mainly with asthma and allergic disease. Must be detail-oriented, well organized with excellent planning and language skills, both oral and verbal, and able to work independently. Responsibilities include screening patients, testing and evaluating patients, documentation, and working with pharmaceutical and regulatory agencies. The candidate should possess knowledge and insight into legal and regulatory matters concerning clinical research. Requires a background in an allied health field, an interest in research, and computer skills.\r
Non-smokers only.\r
\tStrict attention to detail\r
\tHighly developed organizational skills\r
\tAbility to work with multiple study protocols\r
\tExcellent verbal and written communication skills\r
\tInterpersonal and problem-solving skills\r
\tSelf-motivated, results oriented, able to work independently \r
\tAbility to work a flexible schedule with some travel\r
\tCommunicate effectively and tactfully with others within the clinic and especially with the public\r
\tAbility to organize workload to determine priority of duties\r
\tBackground in an allied health field is required although a nursing degree is preferred\r
\tA minimum of one year of experience as a study coordinator preferred; certification in research (ACRP) preferred.\r
\tComputer literacy in word processing, spreadsheet and database applications\r
\tKnowledge of FDA regulations and GCP guidelines preferred\r
\tInternational Air Transport Association (IATA) certification is a plus (will train)\r
\tBLS or must complete within six months of hire\r
\tTasks  \r
\tClinical trial preparation for pharmaceutical protocols\r
\tDevelopment and evaluation of patient information and informed consent forms and patient recruitment\r
\tRecruitment and coordination of the patient with regard to informed consent, screening and inclusion of the subjects adhering to safety and compliance issues\r
\tCoordination and management of the clinical trial, communication with sponsor, visit coordination, sampling, time management and product accountability\r
\tData collection and management, collection of source documents, using and developing CRFs, registration and management of AEs, filing and archiving, managing monitoring visits, dealing with queries\r
\tClose-out of the clinical trial, audit preparation, and trial closure\r
\tAttendance at Investigator Meetings\r

Company info

Asthma & Allergy Center

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