Cardiovascular Research Assistant

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At Avera Heart Hospital youre not just joining a workplace youre becoming part of a family. With more than 700 dedicated employee we deliver care that truly makes a difference. Our commitment to excellence has earned us the distinction of being one of only a handful of hospitals nationwide out of more than 4000 to achieve a double 5-star rating from the Centers for Medicare and Medicaid Services.

Position Highlights

Works under the general direction of cardiovascular research leadership and in collaboration with principal investigators research nurses coordinators physicians advanced practice providers and operational teams. Supports high-quality clinical research involving cardiovascular devices medications heart failure structural and interventional cardiology electrophysiology vascular care prevention and other heart and vascular conditions. Performs diverse administrative data participant-support and study-operational duties in accordance with approved protocols delegated responsibilities institutional policy and applicable regulations.

• Review electronic health records and approved source documents to identify protocol-required data; enter and maintain accurate information in electronic data capture systems study databases registries and tracking tools.
• Support study start-up and maintenance by organizing regulatory documents delegation and training records study logs protocol materials manuals and essential-document files.
• Assist research staff with pre-screening and screening activities by applying approved criteria preparing screening materials tracking potential participants and escalating clinical or eligibility questions to qualified study personnel.
• Coordinate protocol-related appointments tests procedures and follow-up activities across clinic hospital imaging catheterization laboratory electrophysiology heart failure pharmacy and other departments.
• Prepare visit checklists source worksheets participant packets laboratory kits device-study materials and other supplies using the current protocol and schedule of events.
• Process package document and ship research specimens according to protocol laboratory requirements safety procedures and shipping regulations within the employees training and authorization.
• Maintain study calendars screening and enrollment logs visit trackers follow-up schedules and reminders to support protocol compliance and participant retention.
• Support participant communications using approved scripts and workflows; promptly route clinical concerns adverse-event information and urgent questions to licensed or otherwise qualified study personnel.

CARDIOVASCULAR RESEARCH ASSISTANT

• Assist with investigational device accountability and documentation including receipt storage coordination inventory logs use or disposition records and reconciliation as delegated and permitted by protocol and policy.
• Support investigational medication workflows by coordinating with pharmacy and research staff maintaining assigned logs collecting protocol-required information and documenting participant-reported adherence as delegated; does not independently dispense or provide medication guidance.
• Request de-identify when authorized track and upload imaging electrocardiograms hemodynamic data device reports and other study records to approved sponsor or central-review systems.
• Perform quality checks for completeness consistency and timeliness; assist with data queries missing-document follow-up and corrections while preserving an appropriate audit trail.
• Prepare materials and respond to requests for sponsor contract research organization monitor auditor and regulatory visits in coordination with research leadership.
• Track completed research procedures participant status study milestones staff workload and other operational measures needed for study management and reporting.
• Perform literature reviews and evidence searches as directed; organize findings and references for investigators and research staff.
• Provide general administrative support including research-chart preparation document scanning and filing secure communications meeting preparation supply ordering and distribution of study materials.
• Participate in team meetings study training process-improvement work and cross-coverage; perform other duties within role scope as assigned.

Devices

Structural heart interventional rhythm-management hemodynamic-monitoring mechanical-circulatory-support vascular and other cardiovascular technologies.

Medications

Investigational and approved therapies studied in cardiovascular populations including protocol-directed treatment adherence safety and outcomes data.

Heart failure

Acute and chronic heart failure cardiomyopathy remote monitoring transitions of care quality of life and clinical outcomes.

Additional areas

Electrophysiology coronary and peripheral interventions imaging prevention registries real-world evidence and investigator-initiated research.

This role supports but does not independently make clinical decisions; determine final eligibility; obtain informed consent unless specifically trained delegated and permitted; diagnose; prescribe; dispense investigational products; or provide medical advice. Clinical findings and safety concerns are escalated promptly through the studys approved workflow.

The individual must be able to work the hours specified and perform each essential function satisfactorily. Requirements listed below are representative of the knowledge skills and abilities needed. Reasonable accommodations may be made for qualified individuals with disabilities unless doing so creates undue hardship.

• High school diploma or GED equivalent.
• Ability to complete required institutional privacy safety human-subject protection and study-specific training within assigned timeframes.

• Associates or bachelors degree in a health science research or related field.
• One to three years of healthcare clinical research cardiology medical-record data-entry or comparable experience.
• Experience with electronic health records clinical-trial databases or registries research documentation medical terminology and cardiovascular care workflows.

• Strong attention to detail organization follow-through and ability to manage multiple protocols priorities and deadlines.
• Clear and professional written verbal and interpersonal communication with participants families clinicians sponsors and team members.
• Ability to handle protected health information and confidential research information with discretion and in compliance with policy.
• Ability to learn protocol requirements recognize discrepancies or safety information and escalate questions appropriately.

• Apply Averas mission vision core values and social principles in service to patients families colleagues and the community.
• Uphold Averas standards of Communication Attitude Responsiveness and Engagement (CARE).
• Follow approved protocols Good Clinical Practice principles IRB requirements privacy standards sponsor requirements and institutional policies applicable to assigned duties.
• Maintain complete accurate timely and traceable documentation; never backdate obscure or improperly alter research records.
• Work effectively in a multidisciplinary team and coordinate workflow to support a safe respectful productive and audit-ready research environment.

Work is performed in office and healthcare settings and may include clinic hospital procedural laboratory or research areas. The noise level is usually moderate. Depending on assignment there may be potential exposure to communicable disease blood or body fluids sharps chemicals radiation-controlled areas or moving equipment. Employees must follow applicable safety precautions and use required protective equipment. Physical requirements may include extended computer use movement between departments and handling study materials or supplies. HR and Employee Health should validate the final physical-demand classification for the position.