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Clinical Research Coordinator A, Center for Tobacco Research

Employer
UNIVERSITY OF PENNSYLVANIA
Location
Pennsylvania, United States
Closing date
13 Oct 2020

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.

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.

Job Description Summary

The Clinical Research Coordinator A will serve as the point of contact for all study related inquiries and will be responsible for coordinating research related activities per protocol including: recruitment, eligibility screening, data collection and quality assurance. The coordinator will also be responsible for maintaining regulatory materials, preparing submissions and supervising and training staff members

Job Description

The position entails planning and performing research and administrative tasks in an evolving, medium-sized research group that concentrates in tobacco addiction research and clinical trials utilizing medication and behavioral treatments. The successful candidate will have experience collecting research data, interacting with research participants and working well as part of a team. Specific activities include: (1) Providing study recruitment oversight and support. Assign weekly call goals. Coordinate recruitment mailings to clinics and individual participants. Ensure completion of eligibility screens in accordance with projected number of screens to be completed per week (as stipulated by weekly call goal assignments). Review intake charts for accuracy. Complete weekly PennChart reviews and phone screening as needed; (2) Organizing study calendars and coordinating session coverage. Ordering study supplies as needed; (3) Become conversant with all regulatory procedures. Prepare IRB submissions and adverse event reporting documentation. Assign and complete weekly quality assurance assignments and study chart review. Maintain regulatory binders and records. Prepare data and materials for audits, continuing review, and Data Safety Monitoring Board meetings and complete follow-up tasks; (4) Become proficient in standard smoking cessation counseling, as well as other experimental smoking cessation counseling. This will entail prepping and shipping a counseling binder to the participant, conducting 45-60 min counseling sessions, and managing nicotine withdrawal symptoms and medication side effects; (5) Conducting participant sessions and data entry as needed. This includes administering questionnaires and psychological interviews, collecting physiologic data, collecting and processing samples, collecting and reporting side effects, scanning and manually entering data, and counseling study participants.; (6) Overseeing data quality assurance assignments and chart review; (7) Assisting with consent completion by participants and medication preparation and reconciliation as needed. Routine schedule is Mon – Fri, 9am-5:30pm with some evening hours required rarely.

This position is contingent on funding.

Qualifications

Bachelor's Degree with 1-3 years of related experience in research and clinical study methodologies or equivalent combination of education and experience is required. Experience working with the IRB is preferred.

Working Conditions

Office, Library, Computer Room; Requires extensive safety

Physical Effort

Typically sitting at a desk or table; Occasional lifting 25 lb. or less

Job Location - City, State

Philadelphia, Pennsylvania

Department / School

Perelman School of Medicine

Pay Range

$36,401.00 - $65,521.00

Affirmative Action Statement 

Penn adheres to a policy that prohibits discrimination on the basis of race, color, sex, sexual orientation, gender identity, religion, creed, national or ethnic origin, citizenship status, age, disability, veteran status, or any other legally protected class.

Special Requirements 

Background check required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.

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