healthcare
Posted 2 hours agoClinical Research Investigator - Cardiology
Tucson, United StatesOn-site
Responsibilities
- 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.
- 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.
Requirements
- 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.
- 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.
- 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. •
- Background in GI, hepatology, obesity, or cardiology therapeutic areas. How We Work
Contact
- experience more accessible to you, please contact CandidateAccommodations@iterative.health.
Additional details
- 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.
- 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.
- Participate in multiple ongoing pivotal studies including feasibility assessments, first-in-human trials, investigator-initiated studies, and national registries.
- Participate in and contribute to the academic and teaching undertakings of the research program.
- 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.