Clinical Research Coordinator A

Requirements

• Bachelor of Science and 1 to 2 years of experience or equivalent combination of education and experience is required.
• Impeccable organization, verbal, written, and interpersonal skills
• Demonstrate familiarity with word processing, spreadsheet, database, and statistical software, and web-based applications
• Working knowledge of REDCap and SPSS
• 2-4 years of research-related experience preferred
• Job Location - City, State
• Philadelphia, Pennsylvania
• Department / School
• Perelman School of Medicine
• Pay Range
• Equal Opportunity Statement
• The University of Pennsylvania is an equal opportunity employer. Candidates are conside

Benefits

Additional Information

University Overview The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual U.S. News & World Report survey. Penn has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn's distinctive interdisciplinary approach to scholarship and learning. As an employer Penn has been ranked nationally on many occasions with the most recent award from Forbes who named Penn one of America's Best Large Employers in 2023. Penn offers a unique working environment within the city of Philadelphia. The University is situated on a beautiful urban campus, with easy access to a range of educational, cultural, and recreational activities. With its historical significance and landmarks, lively cultural offerings, and wide variety of atmospheres, Philadelphia is the perfect place to call home for work and play. The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator A Job Profile Title Clinical Research Coordinator A Job Description Summary We are seeking a full-time coordinator who will be responsible for assisting with management of Dr. Schnoll's projects within the Center for Interdisciplinary Research on Nicotine Addiction (CIRNA). The goal of these research trials is to apply insights from behavioral economics to rapidly accelerate the pace at which evidence-based practices for cancer care and tobacco treatment are deployed, thereby increasing their reach and impact on the health of individuals with cancer. In this work, the candidate will be required to act autonomously in their decision-making, communicate thoughtfully with the scientific leads and display excellent communication skills and good judgment. Additionally, the candidate will provide limited supervision for some functions and staff within CIRNA. The candidate must have impeccable organization, verbal, written, and interpersonal skills. All applicants must be able to demonstrate familiarity with word processing, spreadsheet, database, statistical software, EMRs, and web-based applications. Working knowledge of REDCap and SPSS are strongly encouraged. This position is contingent on funding. Job Description Job Responsibilities Manage the implementation of projects; oversees recruitment, enrollment and follow-up procedures; align effort across the center; support the management of data collection and analysis of projects; develop and maintain materials and tools for study management and provide timely reports to project leads; track metrics and ensure progress towards study milestones. Manage the design, launch, and sustainment of tobacco treatment & implementation science trials by overseeing recruitment and enrollment; develop and maintain study management tools to facilitate project progress; provide supervision for study staff Manage study-related meetings; prepare all materials necessary to drive activities forward during these meetings and communicate next steps to all attendees after meetings; track all feedback and lead integration of feedback into projects. Assist with preparation of regulatory documentation; support regulatory compliance by maintaining documentation; prepare data for reporting and analysis by contributing to data management Contribute to manuscript preparation and presentations Assist with supervisory responsibilities for study staff via individualized meetings; serve as staff point person for external communications related to research performance Perform additional duties as assigned

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