Holter Monitor Tech 2

As a community, the University of Rochester is defined by a deep commitment to Meliora - Ever Better. Embedded in that ideal are the values we share: equity, leadership, integrity, openness, respect, and accountability. Together, we will set the highest standards for how we treat each other to ensure our community is welcoming to all and is a place where all can thrive.

Job Location (Full Address):

601 Elmwood Ave, Rochester, New York, United States of America, 14642

Opening:

Worker Subtype:

Regular

Time Type:

Time as Reported / Per Diem

Scheduled Weekly Hours:

As Scheduled

Department:

400274 CCRC

Work Shift:

UR - Day (United States of America)

Range:

UR URCC 204 H

Compensation Range:

$19.08 - $25.77

Responsibilities:

GENERAL PURPOSE
Experienced ECG Technician playing a pivotal role in the execution of clinical studies and trials by conducting precise ECG reviews and annotations. This position requires expertise in ECG data management, training of junior staff members, and oversight of logistical operations related to ECG activities.
- Conduct thorough reviews and precise annotations of ECG data collected during clinical studies and trials.
- Ensure compliance with protocol-specific guidelines and standard operating procedures (SOPs) for ECG data collection and analysis.
- Promptly identify and report any anomalies or irregularities in ECG recordings.
- Manage ECG data effectively, including organization, storage, and maintenance of databases in accordance with regulatory requirements.
- Collaborate with the data management team to ensure the accuracy, completeness, and integrity of ECG data.
- Provide comprehensive training and mentorship to junior staff members on ECG procedures, techniques, and data analysis.
- Develop training materials and resources to facilitate the onboarding and professional development of new team members.
- Coordinate logistical aspects of ECG operations, including equipment maintenance, and inventory management.

ESSENTIAL FUNCTIONS

• Assists in the processing, analysis, and reporting of standard ECG and Holter and other ambulatory ECG recordings.

• This requires familiarity with technological concepts associated with commercial Holter annotation systems and other commercial ECG-based products

• Assists in the coordination, preparation, processing, and management of scientific data generated by specialized ECG programs from the commercial and research arenas from local and off-site data management systems, as well as modification of those methodological approaches as appropriate using pre-specified study operating procedures

• Recruits, screens, consents, and enrolls subjects.

• Performs record reviews for local research studies primarily focused on electrocardiographic data collection.

• Reviews medical chart history to verify inclusion criteria are being met.

• Performs procedures as required by protocol (performing electrocardiograms and Holter recordings, while observing electrophysiology, etc.).

• Creates patient instructionsand schedules for patient appointments

• Prepares reports and assists with operating procedures documentation related to ongoing studies including data quality control procedures.

• Demonstrates and maintains professional proficiency and competencyin cardiac arrhythmia recognition and classification

• Maintains the inventory of all ECL hardware as well as the storage, testing, shipment, receipt, and maintenance of ECG Core Laboratory equipment and supplies

• Coordinate logistical aspects of ECG operations, including equipment maintenance, and inventory management.

Other duties as assigned.

MINIMUM EDUCATION & EXPERIENCE

• Associate’s degree or equivalent with courses and/or technical training in electrocardiography or cardiac rhythm interpretation Required.

• And at least 4- 5 years’ experience in electrocardiographic monitoring or related technical work environment Required.

• Or equivalent combination of education and experience Required.

KNOWLEDGE, SKILLS AND ABILITIES

• Applicant must have technical training and a minimum 4-5 years specialized experience in related field, or equivalent combination of education and experience. Required

• Knowledge of PC-based analysis programs helpful including working knowledge of Microsoft Office products (Word, Excel, Outlook). Required

• Experience in using knowledge of cloud storage environments such as BOX and Dropbox, collaborative work environments such as Google Drive, and basic familiarity with REDCap and other clinical trial electronic acquisition systems. Required

• Previous experience with clinical research studies (including FDA-regulated) as well as previous communication experience with research sponsors, enrolling site personnel and patients is desirable. Required

• Applicants must be able to work independently and meet individual and team deadlines. Required

• This position also requires excellent communication skills and a high level of organizational ability and professional interaction.

The University of Rochester is committed to fostering, cultivating, and preserving an inclusive and welcoming culture to advance the University’s Mission to Learn, Discover, Heal, Create – and Make the World Ever Better. In support of our values and those of our society, the University is committed to not discriminating on the basis of age, color, disability, ethnicity, gender identity or expression, genetic information, marital status, military/veteran status, national origin, race, religion, creed, sex, sexual orientation, citizenship status, or any other characteristic protected by federal, state, or local law (Protected Characteristics). This commitment extends to non-discrimination in the administration of our policies, admissions, employment, access, and recruitment of candidates, for all persons consistent with our values and based on applicable law.