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The Research Associate Sr manages day-to-day operations for women's health studies, including participant recruitment, screening, and the administration of clinical procedures. They are also responsible for processing biological samples and supervising junior research staff.
Requires a Master's degree with 1 year of research experience or a Bachelor's degree with 3 years of experience in a related field such as Psychology or Neuroscience. Proficiency with computers and knowledge of research methodology are required.
The Center for Women’s Biobehavioral Health Research (PI: Rebecca Thurston) is devoted to understanding and enhancing women’s health at midlife and beyond. The Center, located in Sterling Plaza, is within the Department of Psychiatry at the University of Pittsburgh. The Research Associate Sr plays a central role in the day-to-day conduct of multiple studies at the Center. Studies include an industry sponsored clinical trial evaluating how a treatment for menopausal hot flashes may impact brain, cognitive, and vascular function in midlife women, and the Study of Women Across the Nation (SWAN) investigation, a longitudinal study generating nationally representative insights into women’s health and experience. The Research Associate Sr work on testing women in at least two studies including the SWAN study and the FAVES-B clinical trial. Both studies recruit women in menopause and measure multiple indices of health and wellness including cognitive functioning. This position will oversee a research specialist working on the same studies. They will trouble shoot research related problems for these two studies on a day-to-day basis.
This position is grant funded.
Responsibilities:
Participate in the day to day activities research studies on women’s health including an interventional clinical trial, including participant recruitment, screening, enrollment, and scheduling in accordance with protocol defined inclusion/exclusion criteria.
Administer protocol adherent execution of all study procedures, including laboratory testing, ambulatory/wearable monitoring, training on electronic diaries, administration of behavioral and neurocognitive assessments, and other study evaluations.
Process blood and related biological samples, including Venipuncture and blood collection from participants, preparation of study equipment and phlebotomy tubes, sample labeling, handling, storage, and transport to designated laboratories in compliance with protocol and safety requirements.
Collaborate closely with investigators, study physician, study coordinator, pharmacists, laboratories, and other stakeholders to support efficient and compliant study execution.
Mentor, train and assist with supervising junior research staff as needed
Enter study data into databases.
Assist with preparation of scientific articles, IRB, and grant submissions as needed.
Perform other duties as assigned.
OR
Licensure, Certifications, and Clearances:
UPMC is an Equal Opportunity Employer/Disability/Veteran
Life Changing Medicine.
UPMC is a world-renowned, nonprofit health care provider and insurer committed to delivering exceptional, people-centered care and community services. Headquartered in Pittsburgh and affiliated with the University of Pittsburgh Schools of the Health Sciences, UPMC is shaping the future of health through clinical and technological innovation, research, and education. Dedicated to advancing the well-being of our diverse communities, we provide nearly $2 billion annually in community benefits, more than any other health system in Pennsylvania. Our 100,000 employees — including more than 5,000 physicians — care for patients across more than 40 hospitals and 800 outpatient sites in Pennsylvania, New York, and Maryland, as well as overseas. UPMC Insurance Services covers more than 4 million members, providing the highest-quality care at the most affordable price. To learn more, visit UPMC.com.
Offices: US Steel Tower, 600 Grant Street, Pittsburgh, PA 15219, US
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