CLINICAL RESEARCH COORD B
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Posted Job Title
CLINICAL RESEARCH COORD B
Perelman School of Medicine
Posted to the Web
Posted Job/Salary Grade
Contingent Upon Funding
Position End Date
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 Penns 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.
The Clinical Research Coordinator A will assist in the coordination of Phase I-IV clinical trials, including coordination, organization and maintenance of all documentation required by the Sponsor or CRO; resolve data queries with Sponsor or CRO; recruit, screen and enroll potential study subjects; participate in the conduct of audits; process and ship blood and specimens; schedule patient visits and any necessary testing; obtain records required to complete case report forms; conduct initiation, monitoring and closeout visits with Sponsor or CRO; adhere to all Penn ICF and FDA guidelines; prepare and process all IRB documentation. The Clinical Research Coordinator B, in addition to above, will manage multicenter clinical trials, including working with partnering institutions on budgets and IRB paperwork. The CRC B will have limited supervision in the management of clinical trials and will need to use more independent judgement.
A Bachelors Degree and 1 year to 3 years of experience or equivalent combination of education and experience is required for the A position. Bachelors degree and 2 years to 4 years of experience or equivalent combination of education and experience is required for the B position. Effective problem solving capabilities; effective communication and writing skills; ability to multitask; demonstrated ability to work as part of a team or independently; knowledge of IRB and human research protection regulations preferred.
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.
Background Check Required
http://jobs. hr. upenn. edu/postings/4450
Posting Supplemental Questions
Required fields are indicated with an asterisk (*).
How did you hear about this employment opportunity?
+ Public Job Posting
+ Internal Job Posting
+ Agency Referral
+ Personal Referral
+ Contacted By a Penn Recruiter
What is your highest level of education?
+ Less than high school education
+ High School Diploma or GED
+ Vocational or Technical School
+ Associate's Degree or Two Year College
+ Bachelor's Degree
+ Master's Degree
+ PHD/MD/JD or equivalent doctoral degree
How many years of experience do you have related to this position?
+ 0 to 1 Year
+ 1 to 2 Years
+ 2 to 3 Years
+ 3 to 5 Years
+ 5 to 7 Years
+ 7 to 10 Years
+ Over 10 Years
A background check may be required for this position. Do you agree to allow a background check to be performed as a condition of employment?
Do you have experience with IRB and human research protection regulations?
Do you have experience assisting in the coordination of Phase I-IV clinical research studies?
Do you have experience with the recruitment, enrollment and follow-up of study subjects for clinical trials?
Do you have budget preparation