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Clinical Research Coordinator-Research-Cardiology
Category
Specialist Clinical Non Clinical
Schedule
Per Diem
Job Number
R0276577
Shift
Varies
Location
Hybrid / Rancho Mirage, CA 92270
Hours
8 Hour Shift*
Department
Research-Cardiology
Salary Range
$ / hour
- For 10 hour and 12 hour shifts this is the average hourly rate which includes overtime when a non-exempt employee works over 8 hours.
Current employees must apply through Workday via the Jobs Hub
Apply Now
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Located in the heart of the Coachella Valley, you have access to resort-style living and world-class amenities throughout Southern California.
- Qualifications
- Job Objective
- Responsibilities
- Essential Skills
Job Description:
Education:
Required: Bachelor's degree in healthcare and/or related field; completion of following CITI Program courses within 30 days of hire: Good Clinical Practice (GCP) Course, Clinical Research Coordinator Foundations Course, Clinical Research Coordinator Advanced Course; courses must be renewed in accordance with institutional policy
Preferred: Master's degree
Licensure/Certification:
Preferred: ACRP CCRC or SOCRA CCRP Certification; certification required upon eligibility
Experience:
Required: Three (3) years current experience in acute care hospital, medical center, health system or related industry
Preferred: Previous experience with clinical trials
Job Objective:
Coordinates and implements clinical research activities.
Essential 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.
Essential Skils:
- Written and verbal communication skills
- Understanding of relevant technologies and tools pertinent to the job role
- Knowledge of good clinical practice (GCP), an international ethical and scientific quality standard for designing, conducting, recording, and reporting trials that involve the participation of human subjects
- Ability to work independently and as a team member
- Ability to use Microsoft Office Suite (Word, Excel, Outlook, PowerPoint) and other relevant software applications
- Ability to prioritize tasks and manage time efficiently to meet deadlines
- Ability to create and maintain positive interpersonal relations with peers, staff, leaders and vendors
- Ability to coordinate multiple projects
- Ability to collect, analyze and disseminate data
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Eisenhower Health offers a generous benefits package and a matched retirement plan.
Employees are eligible to participate in a benefits program designed to make a difference for you and your family.
View Full Benefits
A Culture of Positivity and Support
From the beginning, this organization formed a culture based on strong values, commitments and a passion for service and professional excellence.
What Our Nurses Say
One of my very favorite things about working at Eisenhower Health is the culture on inclusivity that we have and a strong base for evidence-based practice.
Lori
Neonatal Nurse
One of the greatest things about working as a nurse at Eisenhower Health is how much support you get from Administration. We keep on improving the process here. It's a fantastic place to work.
Richard
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My favorite thing about working at Eisenhower Health is the camaraderie within my unit and with the different departments.
Jennifer
Registered Nurse
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39000 Bob Hope Drive,
Rancho Mirage, CA 92270
(760) 837-8500
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