Eisenhower Health · 3 months ago
Clinical Research Coordinator-Per Diem
Eisenhower Medical Center
Full-time
Onsite
Mid Level
$37/hr - $37/hr
3+ years expEisenhower Health is a medical center focused on providing high-quality healthcare services. The Clinical Research Coordinator is responsible for coordinating and implementing clinical research activities, including patient recruitment, monitoring compliance with protocols, and managing clinical trials budgets.
Health CareHospitalMedicalOutpatient CareRehabilitation
Responsibilities
Demonstrates compliance with Code of Conduct and compliance policies, and takes action to resolve compliance questions or concerns and report suspected violations
Recruits, educates, consents, schedules, and completes follow-up with patients/subjects
Participates in the design, planning and conduct of clinical trials program and clinical research projects
Performs pre-investigation, initiation and periodic monitoring visits to assure that the protocol, obligations, responsibilities, and regulations are established and followed
Monitors subject records for quality, data integrity and compliance with regulations and organization’s standard operating procedures (SOP)
Assists in writing and/or auditing clinical reports
Assists in developing protocols, case report forms, and informed consent documents
Works closely and acts as a liaison between sponsors, Contract Research Organization (CRO) sites and other department staff members
Manages the negotiation and monitoring of budgets and contracts; formulates study budgets utilizing the protocol, manuals, study plan and resource needs assessment for the study; develops and supports the development of tools and training to aid in the development of study budgets, coverage analysis, tracking of invoiceable term items and research billing
Performs clinical site activities (regulatory issues, patient accrual, patient scheduling and care coordination, data capture and monitoring, adverse events reporting)
Develops sufficient service/ program / product / indication expertise to communicate directly with clinicians, staff, other departments, consultants and provide consultation/expert advice to leadership
Develops or contributes to the development of SOPs, best practices, tools, processes and training to enhance safety and compliance with federal, local and institutional regulations/guidelines
Manages tracking and reporting Serious Adverse Events (SAEs) and Adverse Events (AEs)
Works with physicians and leadership to develop and implement client trials and research programs; carries out key activities in evaluating, initiating, operationalizing and conducting clinical trials
Works closely with physicians and staff to facilitate research and enrollment to research studies and clinical trials
Prepares and presents materials to Institutional Review Board (IRB); investigates and resolves problems and complaints; develops corrective and preventative action plans
Develops educational/promotional materials to educate patients on available programs and clinical trials; develops and maintains a formal mechanism to ensure that information about the availability of clinical trials is provided to patients
Works to accrue and monitor cases enrolled in program and clinical trials; reports to governing Committee
Coordinates performance improvement activities as they relate to clinical trials and research
Provides support to investigators and maintain screening, enrollment, compliance, statistics on program and trials. Involved in planning long or short term objectives that support research program
Develops and implements Education Program for the community, including materials and lectures
Performs other duties as assigned
Qualification
Required
Bachelor's degree in healthcare and/or related field
Completion of following CITI Program courses: Good Clinical Practice (GCP) Course, Clinical Research Coordinator Foundations, Clinical Research Coordinator Advanced
Three (3) years current experience in acute care hospital, medical center, health system or related industry
Ability to collect, analyze and disseminate data
Ability to coordinate multiple projects
Ability to create and maintain positive interpersonal relations with peers, staff, leaders and vendors
Ability to prioritize tasks and manage time efficiently to meet deadlines
Ability to use Microsoft Office Suite (Word, Excel, Outlook, PowerPoint) and other relevant software applications
Ability to work independently and as a team member
Knowledge of good clinical practice (GCP)
Understanding of relevant technologies and tools pertinent to the job role
Written and verbal communication skills
Preferred
Master's degree
ACRP CCRC or SOCRA CCRP Certification; certification required upon eligibility
Previous experience with clinical trials
Company
Eisenhower Health
Eisenhower Health provides full range of state-of-the-art diagnostic, treatment and emergency facilities.
1001-5000 employees
Funding
Current Stage
Late StageLeadership Team
Ken Wheat
Executive Vice President/COO
Ann Mostofi
CNO, Vice President Patient Care Services
Recent News
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