Women's Health Clinical Research Coordinator

University of Wisconsin; Madison (WI); Híbrido; USD 51 000 - 63 000; Tempo integral

Resumo da oferta

The University of Wisconsin–Madison's Department of Obstetrics and Gynecology seeks a Clinical Research Project Coordinator I to support non-cancer women’s health trials across multiple divisions. You will manage administrative trial activities, activate studies, and coordinate with investigators, sponsors, and sites.

Ideal candidates are organized, collaborative, and eager to advance clinical research through operational excellence and strong relationship management; some work may be onsite

Qualificações

• 2 years employment experience in Clinical Research Coordination and Clinical Trials is required by the start date of the position.
• Bachelor’s Degree preferred; focus in life sciences/healthcare or related field preferred
• University sponsorship is not available for this position, including transfers of sponsorship and TN visas. The selected applicant will be responsible for ensuring their continuous eligibility to work in the United States (i.e. a citizen or national of the United States, a lawful permanent resident, a foreign national authorized to work in the United States without the need of an employer sponsorship) on or before the effective date of appointment.

Responsabilidades

• 5% Designs and develops a system of databases for research data in a format suitable for analysis
• 15% Serves as the primary liaison between the HSC and MFM/Meriter and ASOG clinical staff. Create site specific workflows that are within clinic and protocol limits to fully integrate clinical research as part of clinical care.
• 5% Assist with training of staff
• 20% Serves as a main point of contact for clinical research participants, providing information regarding research procedures, expectations, and informational inquiries. Ensures participants follow the research protocol and alerts Principal Investigator of issues
• 5% Serves as point of contact for external institutions participating in clinical research studies. Ensures data is entered accurately by study team(s)
• 5% Coordinates and assists with development of investigator-initiated study protocols and associated documents, both during initial development and when changes are required.
• 5% Schedules, coordinates, and prepares for sponsor site visits, ensuring that all study records are available, complete, and accurate for sponsor review
• 20% Interfaces with investigators, research staff, sponsors, and collaborators to maintain clinical trials, including reviewing, evaluating, and implementing new protocols, protocol amendments, ensuring timelines and milestones are met; assists with, or is responsible for proper study close-out procedures and communication to ensure proper trial management.
• 20% Collaborates with investigators, research staff, study sponsors, and other collaborators to rapidly move clinical trial research protocols through the activation process. May assist with coordination of and communication related to new clinical trial opportunities

Formação académica

Bachelor’s Degree in life sciences/health care or related field

Descrição da oferta de emprego

The University of Wisconsin–Madison's Department of Obstetrics and Gynecology seeks a Clinical Research Project Coordinator I to support non-cancer women’s health trials across multiple divisions. You will manage administrative trial activities, activate studies, and coordinate with investigators, sponsors, and sites.

Ideal candidates are organized, collaborative, and eager to advance clinical research through operational excellence and strong relationship management; some work may be onsite