Clinical Research Investigator - Cardiology

Iterative Health•Tucson, AZ

15h

About The Position

Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes. We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide. The Clinical Research Investigator at Iterative Health is an integral member of the research team, contributing to the conduct and advancement of multiple ongoing pivotal studies — from feasibility and first-in-human trials to investigator-initiated studies and national registries. This role plays a critical part in the day-to-day execution of clinical research while supporting the academic, training, and operational functions that make our research programs run with excellence. The ideal candidate is a highly organized, analytically driven research professional who is passionate about advancing clinical science and improving patient outcomes through rigorous, high-quality research.

Requirements

Successful completion of a four-year medical degree; completion of or enrollment in a Research Fellowship, or equivalent post-graduate education in biomedical sciences, 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 and critical thinking skills, with the ability to problem-solve and 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.

Nice To Haves

Prior experience in clinical research, investigator-initiated studies, or national registry participation.
Familiarity with GCP guidelines and human subject research regulations.
Experience with data management systems, EDC platforms, or CTMS tools.
Experience preparing and presenting abstracts or case studies at academic or clinical conferences.
Background in GI, hepatology, obesity, or cardiology therapeutic areas.

Responsibilities

Participate in multiple ongoing pivotal studies including feasibility assessments, first-in-human trials, 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 and appointments, administer surveys, collect and aggregate data, and serve as a patient liaison for the Principal Investigator.
Maintain investigational product inventory and required storage conditions.
Maintain required documentation including source documentation, subject logs, records, reports, and other essential study documents.
Participate in and contribute to the academic and teaching undertakings of the research program.
Lead training for incoming fellows and support the development of future investigators in Good Clinical Practice (GCP) principles and human subject research conduct.
Prepare and present abstracts and case studies at meetings and conferences to support department and program development.
Perform data mining, data entry, and data quality management 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 physicians, investigators, clinical research staff, ancillary departments, research subjects, sponsoring organizations, regulatory bodies, vendors, and suppliers.
Participate in weekly research meetings with program and medical directors, biweekly meetings with Principal Investigators, and daily meetings with the discipline's primary coordinator.
Attend meetings and conferences for department/program development, sponsor and trial recruitment, and departmental representation.
Performs related duties as requested