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Manager Clinical Trial Rn Jobs in Iowa (NOW HIRING)

APPS Paramedical Services

Paramedical Examiner

Atlantic, IA · On-site

$25 - $50/hr

We also complete clinical trial blood draws for a rapidly growing clinical trial industry. We are ... Current licensure, certificate of medical training IS NOT REQUIRED FOR THIS POSITION (e.g., RN, LPN ...

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Manager Clinical Trial Rn information

What is the difference between Manager Clinical Trial Rn vs Clinical Research Coordinator?

AspectManager Clinical Trial RnClinical Research Coordinator
CredentialsRegistered Nurse (RN) license, clinical trial experience, possibly certification in researchTypically bachelor's degree in health or related field, research training
Work EnvironmentOversees multiple trials, manages teams, administrative and supervisory dutiesCoordinates daily trial activities, patient interactions, data collection
Employer & Industry UsagePharmaceutical companies, research institutions, hospitalsResearch sites, hospitals, clinics, academic institutions

The Manager Clinical Trial Rn generally has more supervisory responsibilities and clinical expertise, overseeing entire trials and managing staff. In contrast, the Clinical Research Coordinator focuses on daily trial operations and patient interactions. Both roles require research knowledge but differ in scope and seniority.

What cities in Iowa are hiring for Manager Clinical Trial Rn jobs? Cities in Iowa with the most Manager Clinical Trial Rn job openings:
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Clinical/HC Research Associate - Cardiology

Clinical/HC Research Associate - Cardiology

The University Of Iowa

Iowa City, IA • On-site

Other

Posted 18 days ago

University Of Iowa rating

6.9

Company rating: 6.9 out of 10

Based on 85 frontline employees who took The Breakroom Quiz

408th of 555 rated colleges and universities

Job description

BASIC FUNCTION

Apply clinical skills requiring a RN license to deliver and evaluate research protocols in adult cardiac electrophysiology.  Key areas of responsibility include research/clinical activities, protocol development, contracting and study responsibilities, subject recruitment and enrollment, data collection and monitoring, regulatory guidelines and documents, human resources/leadership and financial responsibility.

KEY AREAS OF RESPONSIBILITY

Research/Clinical Activities:

  • Perform clinical/health care research activities for EP research which includes bedside management of subject participants before, during and post interventional procedures.

  • Research activities involve the coordination and collection of research data for subjects with arrhythmias, permanent pacemakers or implantable cardiac defibrillators.

  • Prepare and participate in monitoring visits; may perform activities such as patient assessments and review of medical history and medications prescribed.

  • Assure compliance with study protocol.

  • Obtain and process clinical trial specimens.

  • Dispense study-related medications and document effects.

  • Assist participants with problems related to their protocol therapy such as consultation when calling reporting concerns related to: returning for emergency evaluation in the case of side effects, assisting with emotional problems, questions related to treatment procedures or other related issues.

Protocol Development and Study Responsibilities:

  • Maintain a comprehensive understanding of the study protocol in order to recruit qualifying subjects, administer investigational product, collect required study data and maintain subject safety.

  • Assist in protocol development and provide input into descriptions of routine research procedures.

  • Resolve queries.

  • Perform randomizations.

  • Develop study materials.

  • Assure study visit compliance within window of visit schedule.

Subject Recruitment and Enrollment:

  • Screen, recruit, and obtain informed consents for clinical trials/studies.

  • Provide thorough explanation about clinical trial to potential subjects. Seek out clarification from principal investigator or sub investigator when necessary. 

  • Assist principal investigator to determine subject eligibility.

  • Schedule trial related procedures and visits within required study protocol windows.

  • Assist with subject assessments during study participation.

  • Notify principal investigator or sub-investigator of an abnormal finding when assessing the subject and schedule follow-up as requested.

Data Collection and Monitoring:

  • Collect and enter concise clinical research data required by the sponsors according to the sponsors', Institutional Research Board and Good Clinical Practice requirements

  • Assist with determining validity of data obtained.

Regulatory Guidelines and Documents:

  • Collect and maintain regulatory documents from subjects and assist in preparation of required regulatory forms and documentation according to protocol.

  • Report any reportable events to appropriate party.

Human Resources/Leadership:

  • Adhere to institutional policies and guidelines.

  • May provide functional and/or administrative supervision.

  • Accept direction, assignments, feedback, coaching and counseling to assure outcomes are achieved.

  • Provide direction, assignments, feedback, coaching and counseling to assure outcomes are achieved.

Financial Responsibility:

  • Assist in budget development and management of resources/supplies for study.

  • Contribute to identification of increased cost/inefficient spending and cost containment measures.

QUALIFICATIONS

  • A Bachelor's degree in Nursing or an equivalent combination of education and experience is required.

  • A Current, valid Iowa Registered Nurse license is required.

  • ACLS certification is required.

  • Ability to work some weekends, evenings, and nights per study protocol as required.

  • Excellent written and verbal communication skills are required.

  • 6 months of nursing experience is required.

  • Knowledge of cardiovascular medicine procedures and cardiovascular medicine terminology is required.

  • Recent (within 1 to 5 years) clinical nursing experience is required.

  • Previous nursing experience with the cardiovascular medicine diseases patient population is required. This includes prior experience with telemetry monitoring and IV drug therapy and placement and administration of cardiac specific medications.

  • 6 months of research experience is desirable.

  • Proficient in using electronic medical record systems is desirable.

Position and Application Details

In order to be considered for an interview, applicants must upload the following documents and mark them as a "Relevant File" to the submission:

  • Resume
  • Cover Letter

Job openings are posted for a minimum of 7 calendar days and may be removed from posting and filled any time after the original posting period has ended.

Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to 5 professional references will be requested at a later step in the recruitment process.

For additional questions, please contact ashley-rayer@uiowa.edu.

Additional Information
  • Classification Title: Clinical/HC Research Associate
  • Appointment Type: Professional and Scientific
  • Schedule: Full-time
Compensation
  • Pay Level: 5A
Contact Information
  • Organization: Healthcare
  • Contact Name: Ashley Nelson
  • Contact Email: ashley-rayer@uiowa.edu

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