Clinical Research Coordinator Associate
Company: Stanford University
Location: Stanford
Posted on: May 7, 2024
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Job Description:
The Department of Anesthesiology, Perioperative, and Pain
Medicine, at Stanford University's School of Medicine, is a
world-leading department that offers comprehensive training and
perioperative patient care, pain management, and critical care
medicine as well as cutting-edge research, encompassing a wide
spectrum of programs in basic, translational, clinical, health
services and medical education.The Department of Anesthesiology,
Perioperative, and Pain Medicine at Stanford University is seeking
a Clinical Research Coordinator Associate. The Clinical Research
Coordinator will perform duties related to helping establish and
coordinating moderately complex aspects of one or more clinical
studies. The Clinical Research Coordinator will join a vibrant and
innovative team committed to pediatric sleep, pain, and opioid
research under P.I., Dr. Cornelius Groenewald. This lab includes
multiple NIH funded research projects that collectively aim to
address the impact of the opioid epidemic on children and
adolescents, through identifying factors that contribute to
development of opioid misuse. Lab projects involve questionnaire,
physiological (actigraphy) and opioid use data collection
(electronic medication adherence technology). The Clinical Research
Coordinator will work under close direction of the principal
investigator and research supervisor/manager.At Stanford University
School of Medicine, the work we do touches the lives of those today
and tomorrow. Through education, research, and health care, the
School of Medicine improves health through leadership, diversity,
collaborative discoveries, and innovation in health care. Whether
working in departments with faculty, or in units that support the
school, our staff are a part of teams that propel us on our journey
toward the future of medicine and Precision Health.Stanford is
rooted in a culture of excellence and values innovation,
collaboration, and life-long learning. To foster the talents and
aspirations of our staff, Stanford offers career development
programs, competitive pay that reflects market trends, and benefits
that increase financial stability and promote healthy, fulfilling
lives. An award-winning employer, Stanford offers an exceptional
setting for professionals looking to advance their careers.The
School of Medicine and the Department of Anesthesia are committed
to diversity, equity, and inclusion for its faculty, staff,
residents, postdocs, and fellows. We aim to recruit, support,
retain, and promote diversity in our department.For more
information on our department, please see our website:
https://med.stanford.edu/anesthesia.htmlDuties include:Serve as
primary contact with research participants, sponsors, and
regulatory agencies. Coordinate studies from startup through
close-out.Determine eligibility of and gather consent from study
participants according to protocol. Assist in developing
recruitment strategies.Coordinate collection of study specimens and
processing.Collect and manage patient and laboratory data for
clinical research projects. Manage research project databases,
develop flow sheets and other study related documents, and complete
study documents/case report forms. Ensure compliance with research
protocols, and review and audit case report forms for completion
and accuracy with source documents. Prepare regulatory submissions,
and ensure institutional Review Board renewals are
completed.Assemble study kits for study visits, monitor scheduling
of procedures and charges, coordinate documents, and attend
monitoring meetings with sponsors, acting as primary
contact.Monitor expenditures and adherence to study budgets and
resolve billing issues in collaboration with finance and/or
management staff.Interact with the principal investigator
regularly, ensuring patient safety and adherence to proper study
conduct. Ensure essential documentation and recording of patient
and research data in appropriate files per institutional and
regulatory requirements.Participate in monitor visits and
regulatory audits. Interact with lab members and collaborators to
assist with other studies and tasks as needed.- Other duties may
also be assigned DESIRED QUALIFICATIONS: Knowledge of principals of
clinical research and federal regulations.Ability to effectively
work in a fast paced environment with multiple projects and
timelines.Familiarity with IRB guidelines and regulations.Previous
experience with REDcap and other related database
applications.Previous experience working with children and
families. EDUCATION & EXPERIENCE (REQUIRED):Two year college degree
and two years related work experience or a Bachelor's degree in a
related field or an equivalent combination of related education and
relevant experience. KNOWLEDGE, SKILLS AND ABILITIES
(REQUIRED):
Keywords: Stanford University, Daly City , Clinical Research Coordinator Associate, Accounting, Auditing , Stanford, California
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