University of Pennsylvania PART TIME CLINICAL RESEARCH COORDINATOR in Philadelphia, Pennsylvania

PART TIME CLINICAL RESEARCH COORDINATOR Below you will find the details for the position including any supplementary documentation and questions you should review before applying for the opening. To apply for the position, please click the Apply for this Job link/button.

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Posting Details

Posting Details

Reference Number 40-23797

Posted Job Title PART TIME CLINICAL RESEARCH COORDINATOR

School Name Perelman School of Medicine

Org NE-Neurology

Posted to the Web 09/26/2016

Posted Job/Salary Grade PT/26

Employment Type Exempt

Hours 20.00

Position Type Part Time

Position Schedule M,W 8-5; F 8-noon

Months 12

Position Length Contingent Upon Funding

Position End Date

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.

Duties

The Clinical Research Coordinator will be responsible for the execution of all clinical trial aspects from start to finish, including but not limited to the implementation of clinical protocol requirements for the Neuromuscular Division. The Clinical Research Coordinator will provide support to patients enrolled into clinical trials, facilitate patient/physician communication, communication with primary physicians which will include coordinating all clinical visit activities for assigned studies and be responsible for tracking disease related symptoms, medication side effects, and dispensing and tracking experimental drug use. They will participate as part of a multidisciplinary team member in the care of patients receiving treatment on clinical research protocols to provide optimal health care for Neuromuscular patients. The Clinical Research Coordinator will communicate any updates to the ALS/MDA Center staff concerning drug study patients including any important information (i.e., patient deaths, emergency admissions) to appropriate personnel.The Clinical Research Coordinator will host periodic monitor visits with respective pharmaceutical companies as well as interact with internal physicians and external physicians to recruit appropriate new patients for clinical trials. They will review new protocols for appropriateness and feasibility, coordinate designated studies ensuring that all records are updated and readily available to the department, the university, the sponsor and the Food and Drug Administration upon request. Screening perspective study participants (patients) for clinical trials and drafting the IRB protocol and all IRB correspondence for assigned drug studies will be a major responsibility in this role. Should the use of medical facilities be required for drug studies (i.e., CTRC, EEG lab, Radiology), compliance and cooperation standard should be maintained. The Clinical Research Coordinator will work with the Office of Clinical Research, Department Business Office, and Contracts Manager to develop study budget, help to facilitate budget negotiation, review monthly financial reports for accounting and budgeting of available funds and invoice for study payments. It is expected they will promote organizational values of patient and visitor satisfaction by demonstrating courtesy and respect for patients and their families, visitors and other employees. Providing care for patients in all age groups, demonstrates competence in the assessment, treatment and care of patients served and will be expected to exhibit a professional and compassionate demeanor in performance of duties and to be unfailingly responsive to the needs of patients.Position is contingent on continued funding.

Qualifications

A Bachelor’s Degree and 2 years to 4 of experience or equivalent combination of education and experience is required. The coordinator must be detail oriented, have prior experience with IRB guidelines, policies, human subject research practices and appropriate professional skills in the execution of research protocols. Must have a strong ability to communicate with clinicians, researchers, patients and families. Job will require communication with staff and patients outside of office hours.

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.

Quick Link http://jobs.hr.upenn.edu/postings/21653

Posting Supplemental Questions

Required fields are indicated with an asterisk (*).


  • How did you hear about this employment opportunity?

  • Jobs@Penn

  • Contacted by a Penn Recruiter

  • Referred by a Penn Employee

  • Referred by a friend or family member

  • Higher Education Recruitment Consortium (HERC)

  • Inside Higher Ed

  • Indeed.com

  • Other Internet Advertisement

  • Linkedin

  • Twitter

  • Other Social Media Site

  • Professional Affiliation/Trade Website

  • Diversity Association/Publication Website

  • Heard about it at a conference or career fair

  • Unique Advantage

  • Recruitment and/or staffing agency


  • What is your highest level of education completed?

  • 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


  • Do you have experience assisting in the coordination of Phase I-IV clinical research studies?

  • Yes

  • No


  • Do you have experience managing all aspects of clinical trials, phase I-IV?

  • Yes

  • No


  • Do you have experience writing IRB protocols?

  • Yes

  • No

Applicant Documents

Required Documents

  • Resume

Optional Documents

  • Cover Letter