Job Details

ID #46146166
Estado Nebraska
Ciudad Lincoln
Full-time
Salario USD TBD TBD
Fuente ICON Clinical Research
Showed 2022-10-01
Fecha 2022-10-01
Fecha tope 2022-11-29
Categoría Etcétera
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Patient Recruitment Planning Specialist

Nebraska, Lincoln, 68501 Lincoln USA

Vacancy caducado!

Patient Recruitment Planning Specialist role at ICON: Remote- USA Summary: As a Patient Recruitment Planning Specialist within our team, you will be accountable for the outbound screening and scheduling of participants for clinical trials targeting specific sites and projects as directed, and for ensuring excellent customer service at all times. Our mission within this group is to bring clinical research to as many lives as possible, while delivering unparalleled service and exceptional value to our clinical trial partners and your responsibilities will included but aren’t limited to the following. Duties: + Recognize, exemplify and adhere to ICON's values which center around our commitment to People Clients and Performance. + As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs. + Contact assigned patient leads and perform a tele screen according to approved telescreen questionnaire to determine suitability for trials + Accurately review, enter and edit patient responses and information in the Accellacare CTMS system + Provide patient follow up where necessary + Book patient appointments into the Accellacare CTMS ensuring that entries are accurate and up to date + Attend all Accellacare and study related training and ensure working knowledge of study protocol + Identify appropriate study opportunities for interested volunteers based on knowledge of clinical trials and site locations with little error. + Perform with minimal supervision and support + Mentor other more junior Patient Recruiters where assigned + Collaborating with site managers and PER team in creation of recruitment strategy + Creating call lists with appropriate data filters + Communication with site staff on enrollment updates + Reporting on key performance measures of PRAs + Support training, development and performance management of PRAs + Other duties as assigned To be successful you will need: + Bachelor’s Degree in medicine, science or equivalent degree + Excellent communication, planning and decision-making skills + 1 year of clinical research experience + Must be able to utilize computer-based applications such as Microsoft Office and other web based systems including CTMS systems Benefits of Working in ICON: ICON provides you with the innovative resources to be successful in delivering results, inspiring others and becoming a trusted partner. We offer an exceptional benefits package that includes a comprehensive health plan, retirement plans, highly competitive pay, corporate bonus plan, time away from work, and many other incentives amongst an opportunity to grow your career within ICON. What’s Next? Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity. ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment

Vacancy caducado!

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