Clinical Research Coordinator-Research-Cardiology

Eisenhower Medical Center

  • Palm Desert, CA
  • 2 days ago
    Want to know if you’re a fit?
    Upload your resume and let our AI show you.

    Skills

    • Acute Careunmatched
    • Administrative Skillsunmatched
    • Adverse Eventsunmatched
    • Analysis Skillsunmatched
    • Auditingunmatched
    • Best Practicesunmatched
    • Billingunmatched
    • Blogunmatched
    • Budget Managementunmatched
    • Budgetingunmatched
    • Case Report Form (CRF)unmatched
    • Clinical Researchunmatched
    • Clinical Trialunmatched
    • Communication Skillsunmatched
    • Community Healthunmatched
    • Community Programsunmatched
    • Contract Managementunmatched
    • Contract Research Organization (CRO)unmatched
    • Corrective Actionunmatched
    • Course Coordinationunmatched
    • Data Analysisunmatched
    • Data Collectionunmatched
    • Data Qualityunmatched
    • Develop and Maintain Customersunmatched
    • Diversityunmatched
    • Establish Prioritiesunmatched
    • Facebookunmatched
    • GCP (Good Clinical Practices)unmatched
    • Healthcareunmatched
    • IRB/IEC (Institutional Review Board/Independent Ethics Committee)unmatched
    • Informed Consentunmatched
    • Interpersonal Skillsunmatched
    • Leadershipunmatched
    • Licensed Practical Nurse/Licensed Vocational Nurseunmatched
    • LinkedInunmatched
    • Medical Writingunmatched
    • Microsoft Excelunmatched
    • Microsoft Officeunmatched
    • Microsoft Outlookunmatched
    • Microsoft PowerPointunmatched
    • Microsoft Wordunmatched
    • Multitaskingunmatched
    • Needs Assessmentunmatched
    • Negotiation Skillsunmatched
    • Neonatal Nursingunmatched
    • Nursingunmatched
    • Organizational Skillsunmatched
    • Patient Careunmatched
    • Patient Educationunmatched
    • Patient Follow-upunmatched
    • Performance Managementunmatched
    • Physician Assistantunmatched
    • Presentation/Verbal Skillsunmatched
    • Problem Solving Skillsunmatched
    • Process Improvementunmatched
    • Project/Program Coordinationunmatched
    • Promotional Programsunmatched
    • Registered Nurse (RN)unmatched
    • Regulationsunmatched
    • Regulatory Complianceunmatched
    • Resolve Customer Issuesunmatched
    • Safety Complianceunmatched
    • Safety Trainingunmatched
    • Society of Clinical Research Associates (SoCRA)unmatched
    • Standard Operating Procedures (SOP)unmatched
    • Statistical Programming Languagesunmatched
    • Team Playerunmatched
    • Time Managementunmatched
    • Training Program Developmentunmatched
    • Training/Teaching Materialsunmatched
    • Writing Skillsunmatched

    Description

    ') Eisenhower Health

    • Jobs
    • Nurse Residency Program
    • Benefits
    • Campus
    • Culture
    • Blog
    • Search Jobs
    • User Menu

    Log In

    close Close

    Search for a job

    Search

    Fine tune your search

    • Category expand_more

    • Administrative Support

    • Advanced Practice Providers

    • Dietary and Environmental Services

    • Information Technology

    • Licensed Vocational Nurse

    • Management and Supervision

    • Patient Care Support

    • Registered Nursing

    • Specialist Clinical Non Clinical

    • Technicians

    • Therapists

    • Schedule expand_more

    • Full Time

    • Part Time

    • Per-Diem

    • Shift expand_more

    • Day

    • Evenings

    • Nights

    • Varies

    • Hours expand_more

    • 10 Hour Shift

    • 12 Hour Shift

    • 8 Hour Shift

    • More Options expand_more

    • Sign-On Bonus

    • Remote

    • Hybrid

    Reset 0 Filterclose

    Search

    Opens new window to Facebook Opens new window to Instagram Opens new window to LinkedIn

    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

    • Share Job:
    • Email
    • Facebook
    • Linkedin

    chevron_left Back To Results

    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

    Apply Now

    • Share Job:
    • Email
    • Facebook
    • Linkedin

    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

    Nursing Supervisor

    My favorite thing about working at Eisenhower Health is the camaraderie within my unit and with the different departments.

    Jennifer

    Registered Nurse

    Be a Part of an Award-Winning Team

    Related Posts

    Build Your Career with Advanced Technology at Eisenhower Health

    3 min read

    Advance Your Career as a Nurse Practitioner in Coachella Valley

    3 min read

    Advance Your Career as a Physician Assistant in Coachella Valley

    3 min read

    Follow Us

    • Facebook
    • Instagram
    • LinkedIn

    Eisenhower Health

    39000 Bob Hope Drive,

    Rancho Mirage, CA 92270

    (760) 837-8500

    • Facebook
    • Instagram
    • LinkedIn

    About Eisenhower Health

    • Centers of Excellence
    • Community Health Needs Assessment (opens in a new window)
    • Contact Us (opens in a new window)
    • History of Eisenhower (opens in a new window)
    • Leadership Roster (opens in a new window)
    • Medical Staff Officers & Department Chairs (opens in a new window)
    • Mission Statement (opens in a new window)
    • Officers & Boards (opens in a new window)
    • Campus Partners (opens in a new window)

    Resources

    • Diversity, Equity & Inclusion
    • Nurse Residency Program
    • Awards & Recognition
    • Clinic Careers
    • Relocation Resources
    • Locations

    Eisenhower Health is an equal opportunity employer.

    Site by L7 Creative

    All rights reserved, Eisenhower Health | Privacy Policy | Accessibility Statement

    Eisenhower Health Careers

    Numbers & Facts

    LocationPalm Desert, CA

    Similar Jobs