Clinical Research Coordinator Level I or II (depending on experience)

This listing was posted on Oasis Applicant Tracking.

Clinical Research Coordinator Level I or II (depending on experience)

Location:

Minneapolis, MN

Description:

Summary:The Center for Veterans Research and Education (CVRE), whose mission is helping to support innovative researchand education initiatives that improve the health and well-being of Veterans, is seeking a Clinical ResearchCoordinator II.Project Description:The Clinical Research Coordinator will work as a key team member on the Functional improvement in OSA andCOPD with a Telehealth LifeStyle and Exercise Intervention (FOCuSEd) Study sponsored by the Patient-CenteredOutcomes Research Institute (PCORI). This position is a pulmonary study based at the Minneapolis VA MedicalCenter and will require an individual who understands the principles of scientific investigation and clinical trialsand is capable of in-depth understanding of the study protocol.Nearly 50% of the estimated 24 million Americans with chronic obstructive pulmonary disease (COPD) also haveobstructive sleep apnea (OSA). When combined, these conditions reinforce shortness of breath, reduce exerciseability, and impair quality of life. Excess weight worsens these symptoms, impairing patients’ ability to breathe,exercise, and perform usual activities. Our goal is to find additional resources and strategies to help clinicians aidpatients in their efforts to lose weight and improve their health.Responsibilities:Major duties and responsibilities may include, but are not limited to the following:• Leading recruitment, screening, enrollment, consent, and follow-up of clinical trial participants accordingto study protocol, including:o reviewing medical chartso conducting study visitso completing questionnaires and surveys with study subjectso conducting tests such as pulmonary function testing and six-minute walko capturing direct measurements including biometric measurement from study subjectso timely and accurate data entryo communication with study participants and medical professionalso tracking study activitieso conducting and transcribing qualitative interviewso monitoring site activities, including data quality and adverse events, providing feedback asnecessaryo maintain paper- and electronic data capture forms and study fileso maintain compliance with applicable IRB, human subjects, all training and data security guidelinesand regulations• Track and communicate with patients throughout the study.• Conduct phlebotomy, urine collection and saliva sample collection per the study.• Process blood, urine, and saliva samples (restricted to centrifugation and preparing sample tubes forshipping).• Maintain timely completion of regulatory documents.• Communicate on a regular basis with the coordinating center.• Develop systems improvements for conduct of the study locally.• Organize and participate in outreach and engagement events with the local Veteran community.• Perform complex tasks, coordinate processes and get involved in decision-making.• Performs all other duties as assigned.Applicants must include a cover letter.Minimum Qualifications:Education: Bachelor’s Degree required (Master’s preferred)Experience: 0-2 years experience for CRC I and 2-4 years of experience required for CRC IIPreferred working knowledge of the studyExperience in research compliance regulationsExperience in clinical health careLicensure/Registration/Certification: None indicated.Preferred Knowledge, Skills, and Abilities:• Demonstrated ability to organize and coordinate work within schedule constraints and handle emergentrequirements in a timely manner.• High attention to detail.• Ability to work in a collaborative team environment.• Demonstrated ability to monitor important and complex projects concurrently.• Knowledge of Microsoft Word, Excel, PowerPoint, and Outlook software.• Demonstrated ability to effectively communicate verbally and in writing, to include writing and preparingmemorandums, letters, and other official correspondence.• Electronic medical record systems• Electronic data capture systems, e.g. REDCap, QualtricsConditions of Employment• Subject to a criminal and educational background check.• Designated and/or random drug testing may be required.• Regular and predictable attendance is required.• Typical hours fall within standard business hours, work may be required during hours beyond standardbusiness hours, including weekends.• Must be a US citizen.Physical Requirements: The employee must be able to navigate the medical center, use a keyboard, and lift 25lbs. Reasonable accommodation may be considered in determining an applicant's ability to perform theduties/functions of the position.Diversity, Equity, and Inclusion: Diversity enriches research and promotes the best healthcare. We arecommitted to building and sustaining an equitable and inclusive environment. We encourage individuals whosebackgrounds or interests align with this commitment, as well as individuals from all backgrounds that areunderrepresented in research, to apply.

Company:

Center For Veterans Research And Education

Posted:

January 25 on Oasis Applicant Tracking

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Clinical Research Coordinator Level I or II (depending on experience) | Clinical Coordinator, Clin1

Clinical Research Coordinator Level I or II (depending on experience)

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