Clinical Research Investigator - Cardiology

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. 

Where You’ll Drive Impact 

• 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

What You Bring to the Team 

• 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.

• 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.

How We Work 

• Collaborative and low-ego team environment
• High ownership and accountability culture
• Fast-paced and highly iterative growth environment
• Open communication and continuous learning mindset
• Mission-driven organization focused on improving patient outcomes
• Comfortable navigating evolving business priorities and opportunities