Advancing New Standards in Reproductive Health (ANSIRH) seeks two Clinical Research Coordinators (CRCs) to conduct participant recruitment and data collection in English and Spanish for the ADAPT (Attitudes and Decision-making After Pregnancy Test) Study. The ADAPT Study is a longitudinal study examining women’s pregnancy decision-making and the effects of pregnancy on women’s lives. We will recruit approximately 2,200 non-pregnant women at risk of pregnancy from participating family planning, primary care, and abortion facilities in the Southwest (i.e., Arizona, Nevada, New Mexico, and Texas). Participants will be followed with confidential surveys administered electronically (online) and / or by phone.
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The Advancing New Standards in Reproductive Health (ANSIRH) program seeks an experienced administrative operations professional to manage operations, assist with short and long-term planning, and improve administrative processes for an office of approximately 50 staff members.
The Administrative Manager will coordinate and perform multiple essential components of the program including human resources, finance, Information Technology (IT), space / facilities, communication, and other administrative functions that vary in scope and complexity. Specific duties include developing and implementing systems related to employee onboarding and training, staff inclusion and engagement activities, managing space planning, supply inventory, and vendor relations, including IT and other contractors.
ANSIRH seeks a Project Director to provide overall operational management for a diverse portfolio of research activities. The Project Director will work closely with Ushma Upadhyay, PhD. MPH, Associate Professor in the Department of Obstetrics, Gynecology, and Reproductive Sciences to help manage several studies including a clinical trial testing the efficacy and safety of a distribution method for medication abortion through telemedicine.
The position requires expert and efficient integration of multiple complex programmatic activities, applying a sophisticated medical knowledge base, expertise in information and communication technologies, substantial leadership skills, and effective collaboration with a variety of people and organizations [clinicians, investigators, clinical staff, administration, Internal Review Board (IRB), human resources, contracts and grants, funders, health centers, Food & Drug Administration (FDA)].
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