Clinical Research Coordinator, Clinical Research Unit - Georgetown University Medical Center

Location
Washington D.C.
Posted
Oct 15, 2019
Institution Type
Four-Year Institution


Clinical Research Coordinator, Clinical Research Unit - Georgetown University Medical Center

Located in a historic neighborhood in the nation's capital, Georgetown offers rigorous academic programs, a global perspective, exciting ways to take advantage of Washington, D.C., and a commitment to social justice. Our community is a tight knit group of remarkable individuals interested in intellectual inquiry and making a difference in the world.

Requirements

Clinical Research Coordinator, Clinical Research Unit - Georgetown University Medical Center

The Georgetown University Clinical Research Unit (GU-CRU / CRU) mission is to sustain specialized institutional resources in which clinical investigators can observe and study human physiology as well as study and treat disease with innovative approaches. The objective of the GU-CRU program is to make available to medical scientists the resources that are necessary for the conduct of clinical research.

The Clinical Research Coordinator is responsible for ensuring that all aspects of clinical trials implementation are conducted smoothly and in a safe manner. The subjects, PIs, sponsors, and the institution depend on the study coordinator for accurate and safe implementation of the clinical protocol. Errors in study conduct result in protocol deviations, which jeopardize the integrity of the clinical data, the reputation of the PI and institution and the safety of the subject. The Coordinator will be responsible for coordination of multiple clinical trials for multiple investigators.

Reporting to the study PI, duties include but are not limited to:
  • Coordinate and participate in clinical research studies conducted by principal investigator(s) at Georgetown University Clinical Research Unit (CRU).
  • Coordinate and participate in a variety of complex activities involved in the collection, compilation, and documentation of clinical research data.
  • Coordinate study initiation tasks including all regulatory documentation and subject recruitment, study enrollment tasks, study conduct, and study closeout.
  • Study conduct will include obtaining blood samples, cultures, tissues and other specimens for laboratory analysis, questionnaires, and data management as indicated and allowable under the state board practice act.
  • Participate in training to obtain certifications and ensure Good Clinical Practices are followed.
  • Required to comply with institutional policies regarding data management and usage of OnCore Clinical Trial Management System (CTMS) as applicable.

Qualifications
  • Minimum qualifications include a Bachelor's Degree preferred or an Associate's degree with one to two years' experience. Consideration given to an equivalent of education and work experiences that demonstrate aptitude for research facilitation.
  • Strong organizational skills.
  • Excellent interpersonal, written and organizational communication skills.
  • Detail oriented with excellent analytical skills.
  • Demonstrated ability to maintain confidentiality.

Preferred Qualifications
  • Experience in a healthcare setting preferred.


Current Georgetown Employees:
If you currently work at Georgetown University, please exit this website and login to GMS (gms.georgetown.edu) using your Net ID and password. Then select the Career worklet on your GMS Home dashboard to view Jobs at Georgetown.

Submission Guidelines:
Please note that in order to be considered an applicant for any position at Georgetown University you must submit a cover letter and resume for each position of interest for which you believe you are qualified. These documents are not kept on file for future positions.

Need Assistance:
If you are a qualified individual with a disability and need a reasonable accommodation for any part of the application and hiring process, please click here for more information, or contact the Office of Institutional Diversity, Equity, and Affirmative Action (IDEAA) at 202-687-4798 or [email protected].

Need some assistance with the application process? Please call 202-687-2500. For more information about the suite of benefits, professional development and community involvement opportunities that make up Georgetown's commitment to its employees, please visit the Georgetown Works website.

EEO Statement:
Georgetown University is an Equal Opportunity/Affirmative Action Employer fully dedicated to achieving a diverse faculty and staff. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to race, color, religion, national origin, age, sex (including pregnancy, gender identity and expression, and sexual orientation), disability status, protected veteran status, or any other characteristic protected by law.

Benefits:
Georgetown University offers a wide variety of comprehensive and competitive benefits. Benefits packages include comprehensive health, dental and vision plans, disability and life insurance coverage, retirement savings programs, tuition assistance, voluntary insurance options (including group legal, accident, and critical illness), and much more. Whatever your need, the Office of Faculty and Staff Benefits will be standing by to support you. You can learn more about the benefits offered to eligible faculty and staff at https://benefits.georgetown.edu or view the online interactive benefits guide for more information.


To apply, visit https://georgetown.wd1.myworkdayjobs.com/en-US/Georgetown_Admin_Careers/job/Medical-Center/Clinical-Research-Coordinator--Clinical-Research-Unit---Georgetown-University-Medical-Center_JR07812





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