Clinical Documentation Jobs in North Chicago, IL

Position: Epic ClinDoc Principal Trainer Location: Online (Locals preferred) Client: State of North Carolina Duration: 12 Months Job Description: We are seeking an experienced Epiccertified Principal Trainer for the EpicCare Clinical Documentation curriculum focused on training end us More...

Acts as a specialized liaison to assist sites with a protocoltailored approach to increase efficiency of the patient identification and recruitment processAssists sites in developing and implementing patient enrollment techniquesCoordinates site specific patient recruitment and retent More...

Purpose :The Clinical Research Nurse is a specialized research professional working with and under the direction ofthe clinical Principal Investigator (PI). Assists with the execution of studyrelated activities of a Phase Iclinical research study. Research nurses should primarily be c More...

Experienced Epiccertified Principal Trainer (PTs) needed for Long Term Care (EpicCare Clinical Documentation) and Intermediate Care Facility (EpicCare ClinicalDocumentation) end users super users and trainthetrainer training. Experienced Epiccertified Principal Trainer (PT) needed fo More...

Description: The ideal candidate will have thorough knowledge of Clinical investigation of medical devices for human subjects Good Clinical Practice (ISO 14155) 21 CFR partand other applicable regulations. Roles & Responsibilities: Contribute to all clinical research activitie More...

Job Title: Clinical Data Associate Duration: 06 months contract with possible extension Shift Details: Day shift/ Fully Remote Pay Range: $30$37 /hr w2 Essential Duties and Responsibilities: Works collaboratively with Process Engineers and Statisticians in Global Manufact More...

Communicates/presents key Clinical Pharmacology information/strategy to senior and executive management regulatory agencies and external peers. Supports strategic planning for drug development activities and projects to achieve departmental strategies goals and objectives. Utilizes sc More...

JOB TITLE: Vendor Qualification Associate I Onsite: Foster City Hybrid: 3 days a week minimum Description Client is looking for a Vendor Qualification Associate I who will report to the Senior Manager of Vendor Outsourcing. The candidate will be responsible for ensuring high quality More...

Industry: HealthcareClinical Nurse Specialist CVICULocation: Santa Clara CAResponsibilities:Clinical Expertise: Provide expert consultation and guidance to nurses and other healthcare providers in the CVICU.Education & Mentorship: Develop and implement educational programs for nu More...

Description: Works collaboratively with Process Engineers and Statisticians in Global Manufacturing Sciences and Technology (GMSAT) Statistical Sciences & Analytics (SS&A) team to meet project deliverables and timelines to author and approve Continued Process Verification (CPV) relat More...

As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigato More...

Description: Job Title: Clinical Trials Management Associate II Location: Foster City CA Duration: 06 months with possible extension Shift Details: 1st shift/ Monday Friday 8am5pm/business hours Essential Duties and Responsibilities Leads or manage components of Phase I II More...

Opportunity at a GlanceThe primary purpose of this role is to establish clinical relationships in markets where new campus  location are likely to open and to support new programs.ResponsibilitiesDevelop relationships with health organizations in potential and current markets.Dev More...

As a Senior CRA you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigato More...

Coordinates investigator/ site feasibility and identification process as well as study startup.Monitors project timelines and patient enrollment implements respective corrective and preventive measures.Reviews monitoring visit reports for all visit types and ensures reporting complian More...

Purpose:Conceive and execute novel scientific research or development in Clinical Pharmacology that achieves projects and Clinical Pharmacology and Pharmacometrics (CPPM) goals. Generate new PK/PD proposals and lead those efforts. Investigate identify develop and optimize new methods More...

The Clinical Site Payment Analyst is responsible for all clinical site payment activity from contract execution through final payment reconciliation include support to internal stakeholders and suppliers.ResponsibilitiesContracts entry and configuration for executed clinical study agr More...

Compliance Manager Clinical Process Compliance is accountable for the interpretation and application of GCP compliance and quality principles as they relate to clinical trial execution. Responsible for facilitating impact assessments of regulatory intelligence working with business pa More...

Communicates/presents key Clinical Pharmacology information/strategy to senior and executive management regulatory agencies and external peers. Supports strategic planning for drug development activities and projects to achieve departmental strategies goals and objectives. Utilizes sc More...

As a Clinical Research Associate you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical site More...