Jody Evenson, Ccrc

Jody Evenson, Ccrc Email and Phone Number

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Jody Evenson, Ccrc's Location
Andover, Minnesota, United States, United States
Jody Evenson, Ccrc's Contact Details

Jody Evenson, Ccrc work email

Jody Evenson, Ccrc personal email

n/a
About Jody Evenson, Ccrc

Certified Clinical Research Coordinator with over ten years of experience managing the clinical research process. I have worked in both Sponsor and Healthcare industries. Naturally analytical with a drive for process improvement. Experienced in the medical device industry (both Cardiac and Neuromodulation). Also comfortable with direct patient (pediatric/parent) interaction. Specialties:Clinical Research Coordinator, HUD/HDE Therapies, IRB Submissions, Writing Guidelines and Work Instructions, Remediation, Customer Service, Quality Assurance, Team Focused Approach, IDE Study Start-up, Regulatory Documentation, GCP, Microsoft Office Suite.

Jody Evenson, Ccrc's Current Company Details
Medtronic

Medtronic

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Jody Evenson, Ccrc Work Experience Details
  • Medtronic
    Technical Services Consultant
    Medtronic Jan 2015 - Present
    Diagnostics and Monitoring division
  • Medtronic
    Clinical Research Associate
    Medtronic Jul 2012 - Jan 2015
    Fridley, Mn
    Enterra HDE TherapyResponsible for front-line management of incoming IRB approvals and SOP and/or FDA required documentation for the Enterra HDE therapy. Act as first point of contact for investigators/site and field personnel regarding regulatory issues. Adhesive ENS Boot StudyResponsible for managing study start-up documentation; created case report forms instructions, informed consent templates, letters of agreement, investigator and site correspondence, and payment schedules. Manage subject enrollment, recruitment, and appointment schedule. Interstim FES (Functional Electrical Stimulation) StudyCollaborate with study manager to define investigator selection criteria, patient recruitment analysis, and create of trial documents
  • University Of Minnesota
    Research Project Manager
    University Of Minnesota Feb 2012 - Jun 2012
    Responsible to generate budgets for clinical research studies including PI-initiated, NIH, and Business and Industry. Develop cost estimates, reconcile, and invoice against research study budgets.Wrote scientific review in prep for committee submissions.
  • Gillette Children'S Specialty Healthcare
    Clinical Reseach Coordinator
    Gillette Children'S Specialty Healthcare Sep 2008 - Feb 2012
    St. Paul, Mn
    Prepares for clinical start-up process including creation of study protocol, informed consent, case report forms (CRFs), developing viable contracts and study budgets. In charge of completing and maintaining IRB documentation. Accountable to screen, recruit, and consent subjects based on protocol eligibility and conduct data collection. Compiles protocol activity, enrollment data, study financials. Reports study adverse events, protocol deviations and sponsor-initiated management. • Researched, interviewed, and identified CTMS vendors in order to provide a streamline manage clinical study documents, study metrics and financials.• Developed new guidelines and established best practices.
  • Boston Scientific
    Latitude Physician Consultant
    Boston Scientific Mar 2005 - Sep 2008
    Shoreview, Mn
    Provides front-line 24/7 technical support to internal and external customers in a call-center environment. Educate, support, and train customers through phone consultation, training programs, written correspondence, and general field assistance. Analyze, troubleshoot, and make recommendations for optimal Latitude system operation.
  • Boston Scientific
    Clinical Research Specialist
    Boston Scientific Jun 1999 - Mar 2005
    Shoreview, Mn
    Responsible to create, compile and verify FDA, Legal, and Financial-required start up documentation is in place for a successful research study start-up. Accountable to monitor study enrollment activities, provide routine status communications to field and site personnel. Managed inventory levels, initiated shipments, and monitored expiration dates of investigational products; Initiated payments and site agreements to external customers. Assigned appropriate study randomization schedule.

Jody Evenson, Ccrc Skills

Research Coordinator Clinical Research Informed Consent Clinical Data Management Clinical Study Design Fda Hipaa Research Ctms Clinical Research Experience Process Improvement Gcps Code Of Federal Regulations Ccrc Icfs Study Coordination Data Collection Case Report Forms Contract Negotiation Audit Support Study Start Ups Research Budgets Ide Studies Heart Failure Medical Devices Humanitarian Device Therapies Clinical Monitoring Clinical Trials Protocol Clinical Development Gcp Healthcare Cardiology Quality Assurance Biotechnology

Jody Evenson, Ccrc Education Details

Frequently Asked Questions about Jody Evenson, Ccrc

What company does Jody Evenson, Ccrc work for?

Jody Evenson, Ccrc works for Medtronic

What is Jody Evenson, Ccrc's role at the current company?

Jody Evenson, Ccrc's current role is at.

What is Jody Evenson, Ccrc's email address?

Jody Evenson, Ccrc's email address is jo****@****nic.com

What schools did Jody Evenson, Ccrc attend?

Jody Evenson, Ccrc attended University Of Wisconsin-Eau Claire.

What skills is Jody Evenson, Ccrc known for?

Jody Evenson, Ccrc has skills like Research Coordinator, Clinical Research, Informed Consent, Clinical Data Management, Clinical Study Design, Fda, Hipaa, Research, Ctms, Clinical Research Experience, Process Improvement, Gcps.

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