Clinical Research Sub Investigator - Cardiology

Iterative Health•Tucson, AZ

14h

About The Position

The Clinical Research Sub-Investigator at Iterative Health sits at a unique intersection of engineering expertise and clinical research — contributing to the conduct of cardiovascular studies, investigational device trials, and investigator-initiated research that directly advances patient care. This role plays a critical part in the day-to-day execution of active studies while supporting the academic and operational functions that drive research excellence across our network. The ideal candidate is a highly organized, analytically driven professional with an engineering background and a passion for translating biomedical innovation into meaningful patient outcomes.

Requirements

Completion of or enrollment in a Research Fellowship, or equivalent post-graduate education in biomedical sciences, engineering, public health, or a related field.
2+ years of experience working with clients, patients, or research participants, or equivalent health or public service experience.
Proficiency in Microsoft Office Suite, including Excel and PowerPoint; familiarity with spreadsheets and statistical data required.
Knowledge of patient care and assessment best practices and related clinical components.
Knowledge of regulations and policies related to patient research, evaluation, care, and information.
Ability to read, analyze, and interpret professional journals, technical procedures, and governmental regulations.
Strong written and verbal communication skills, including the ability to write reports, correspondence, and procedure protocols.
Highly organized with the ability to manage multiple priorities simultaneously.
Strong analytical, critical thinking, and problem-solving skills with the ability to make sound decisions.
Ability to work effectively with diverse populations, demonstrating compassion, cultural sensitivity, and emotional support throughout the care continuum.
Ability to work both independently and collaboratively in a fast-paced, self-directed environment.
Professional, positive attitude and composure in high-pressure situations.

Responsibilities

Participate in multiple ongoing cardiovascular studies, investigator-initiated studies, and national registries.
Facilitate and coordinate daily clinical research activities, playing a critical role in the conduct of all active studies.
Conduct participant interviews, schedule appointments, administer surveys, collect and aggregate data, and serve as a patient liaison for the Principal Investigator.
Maintain required documentation including source documentation, subject logs, records, reports, and other essential study documents.
Participate in and contribute to the undertakings of the cardiovascular research program and investigational devices.
Prepare and present abstracts and case studies to support department and program development.
Participate in weekly research meetings with the Program Director; work closely with investigators, faculty, physicians, and research staff on a daily basis.
Perform data mining and data entry across active research programs.
Prepare detailed reports providing a range of data to assist management in evaluating performance and making recommendations.
Identify positive or negative variances from expected outcomes and escalate findings appropriately.
Act as a liaison between research staff, ancillary departments, research subjects, sponsoring organizations, regulatory bodies, vendors, and suppliers.
Communicate effectively with patients, their representatives, and the general public in a compassionate, culturally sensitive manner.
Performs related duties as requested