Clinical Research Coordinator III

Department

BSD OBG - Maternal Fetal Medicine

About the Department

The Department of Obstetrics and Gynecology has 114 clinical providers, providing care at the main hospital in Hyde Park and seven off site locations. The Department consists of seven sections: General Obstetrics and Gynecology, Maternal Fetal Medicine, Family Planning, Reproductive Endocrinology and Infertility, Gynecologic Oncology, Urogynecology, and Minimally Invasive Gynecologic Surgery. We have More than 60,000 outpatient visits, 25,000 ultrasound visits, 2,800 deliveries, 3,000 gynecological surgeries per year. Teaching, research and the highest quality clinical care are top priorities for the Department. The residency and fellowship programs are highly ranked and have a history of training leaders in healthcare. The Department also has a significant research enterprise, engaging in population health studies, as well as research conducted in wet laboratories on tumor biology, fibroids and the mechanisms of hypertensive diseases in pregnancy. This at-will position is wholly or partially funded by contractual grant funding which is renewed under provisions set by the grantor of the con¬ tract. Employment will be contingent upon the continued receipt of these grant funds and satisfactory job performance. This at-will position is wholly or partially funded by contractual grant funding which is renewed under provisions set by the grantor of the contract. Employment will be contingent upon the continued receipt of these grant funds and satisfactory job performance.

Job Summary

The job performs routine assignments related to the documentation, analysis, and reporting of research data. Provides input to support the strategic, administrative, operational, and financial decisions that impact clinical research conducted across the University.

Manages medium to highly complex studies by providing input to support the strategic, administrative, operational, and financial decisions that impact clinical research conducted across the University with minimal oversight. The job functions as the manager of the postpartum remote patient monitoring program at the University. The job performs routine assignments related to scientific research projects. Ensures compliance of research activities with institutional, state, and federal regulatory policies, procedures, directives and mandates. Analyzes possible solutions using standard procedures. Writes articles, reports and manuscripts. Assists in drafting presentations on research findings. The job performs training and mentorship for lower-level positions.

Responsibilities

• Responsible for three major studies- all aspects:

  • Aspirin to Prevent Cardiac Dysfunction in Preeclampsia- NIH funded RCT.

  • STAMPP HTN- remote patient monitroing for all patients with PPHTN at UCM.

  • BRIDGE- Biomarkers Registry for Investigating Data and Guiding Evaluation in Preeclampsia. A mutli site study funded by Thermo Fisher.

  • Participate as research assistant in 'Luteolin road map'- study funded by Gates Foundation.

• Under minimal supervision, will collaborate with faculty, clinical staff, support staff, other researchers, residents, and medical students to provide technical and administrative support, as well as development and analysis of both qualitative and quantitative research.

• Manage a remote patient monitoring program for 80-90 pregnant patients per month with hypertensive disorders and lead full cycle clinical research trials focused on these conditions.

• Coordinating study logistics, including participant recruitment, data collection, and data management; drafting study instruments and protocols; assisting in training and protocol development.

• Collecting data using surveys, medical chart reviews, interviews, focus groups, and other techniques; analyzing data and presenting study findings.

• Ensuring compliance with institutional and regulatory guidelines.

• Researching new study opportunities.

• Oversee day-today operations of multiple complex clinical trials, including multi-site trials, from initiation to close-out.

• Managing study budgets, contracts and monitor expenses for NIH R01 funded RCT .

• Maintaining IRB submissions, protocol amendments, and sponsor guidelines.

• Serves as primary point of contact for sponsors, and CROs (Contract Research Organizations) and regulatory bodies.

• Serves as consultant for remote patient monitoring program start up.

• Maintain relationships with external partners and stakeholders, ensuring their needs and expectations are met.

• Coordinate sponsor meetings, update reports, and handle any issues or escalations related to the program.