Clinical Research Coordinator (3618)

Brooks Rehabilitation; Jacksonville (FL); Sur place; USD 45 000 - 65 000; Plein temps

Résumé du poste

Brooks Rehabilitation is seeking a Clinical Research Coordinator I to contribute to the Brooks Center for Innovation. The CRC-I will assist in collecting and documenting clinical research data, coordinate regulatory processes, and support study personnel in conducting procedures.

The ideal candidate has a Bachelor's degree, at least 1 year of research experience, and strong planning, communication, and analytical skills. CPR certification and knowledge of regulatory guidelines are preferred.

Qualifications

• Bachelor's degree required.
• At least 1 year of research experience preferred.
• Strong planning, management, organization and communication skills.
• Knowledge of state and federal clinical research regulations is preferred.
• Proficiency with Windows and web-based applications.
• Basic Life Support (CPR) certification required.
• Excellent verbal and written communication skills.

Responsabilités

• Assist in study monitoring/auditing visits.
• Assist study personnel in conducting study procedures.
• Conduct informed consent.
• Conduct initial screening calls/visits with potential participants.
• Document and communicate AE/SAEs to appropriate study personnel.
• Maintain study documentation in accordance with rules and regulations governing research.
• Maintain study metrics in adherence with reporting procedures.
• Prepare IRB documents and contracts and assist in preparing/submitting IRB materials.

Connaissances

Planning

Management

Organization

Communication

Collaboration

Analytical skills

Leadership

Self-motivation

Self-regulation

Verbal communication

Written communication

Formation

Bachelor's degree

Outils

Windows

Web-based applications

Description du poste

DescriptionO pportunity for a clever and enthusiastic individual to make an important contribution to the Brooks mission by working with the Brooks Center for Innovation. The Clinical Research Coordinator I (CRC-I) participates in a variety of complex activities involved in the collection, compilation, documentation and analysis of clinical research data for assigned protocols and assists in ensuring current and accurate reporting and tracking information is maintained for assigned studies. Under the direction of the Principal Investigator(s), Research Manager, Senior Research Associate or other senior level staff the CRC-I may coordinate and perform study specific regulatory processes and procedures or assist other study personnel in doing so. The CRC-I may also conduct study related recruitment, assessments, measurements or interventions as appropriate. The CRC-I may be assigned direct responsibility as the coordinator for one or more projects and may also have general responsibilities for one or more additional projects.SUPERVISES: Non-supervisoryJob Responsibilities:Assist in preparing for study monitoring/auditing visitsAssist study personnel in conducting study proceduresConduct informed consentConduct initial screening calls/visits with potential participantsDocument and communicate of AE/SAEs to appropriate study personnelIdentify situations when involvement of primary investigators is needed.Initiate and follow through with experimental protocols independent of primary investigators.Input data and perform documentation in accordance with study proceduresMaintain study documentation in accordance to rules and regulations governing researchMaintain study metrics in adherence with reporting proceduresMonitor currency of study personnel's training and certificationsParticipate in Center for Innovation initiativesPlan study sessions and ensuring availability of required resourcesPrepare documents and equipment/space prior to study visitsPrepare lists of potential participants for screeningRead and extract relevant information from medical records.Schedule screening calls/visitsSchedule study visits in accordance with protocolServe as primary contact for general study inquiriesSubmit requests for medical recordsAssist VP, Clinical Integration and Research in developing research contracts and preparing/submitting IRB documents.Work with the Center for Innovation team in conducting literature reviews for relevant research topicsJob Qualifications:Minimum of a Bachelor’s degree. At least 1 year of previous research experience is desired.Strong and demonstrable planning, management, organization, communication, collaborative and analytical skills are required .Basic Life Support (CPR) required.Current knowledge of state and federal rules, regulations, and standards governing clinical research is preferred.Proficiency with Windows and web-based applications required.Requires leadership skills and must demonstrate high level of self-motivation and self-regulation.Must demonstrate excellent verbal/written communication skills.Disclaimer: This job description describes the general nature and level of work only. It is not an exhaustive list of all responsibilities, duties, and skills. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.Qualifications