Study Activation Coordinato, Clinical Research Management Office, Lombardi Comprehensive Cancer Ctr

Job description



Study Activation Coordinator for Clinical Research Management Office, Lombardi Comprehensive Cancer Center Georgetown University Medical Center (GUMC)

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

Study Activation Coordinator for Clinical Research Management Office, Lombardi Comprehensive Cancer Center - Georgetown University Medical Center (GUMC)

Georgetown's Lombardi Comprehensive Cancer Center (LCCC) committed to recruiting, educating, and developing the careers of the next generation of outstanding basic and clinical cancer researchers who will continue the fight against cancer.

The Study Activation Coordinator monitors the progress of clinical trials throughout the study activation process within the LCCC's CRMO) in pursuit of efficient, competitive study activation timelines; and works with key stakeholders in a variety of departments and functional areas to identify barriers, develop solutions, and communicate progress.

Reporting to the Regulatory Manager, the Study Activation Coordinator has primary duties that include but are not limited to:

  • Facilitate the study activation process as by serving as a liaison between Georgetown University departments and LCCC CRMO functional unit, including for example, the regulatory and finance teams, and various internal protocol review bodies
  • Manage clinical research activation timelines and activity by monitoring clinical research submissions - including affiliate or network sites - to ensure efficiency and accuracy
  • Communicate study updates to appropriate stakeholders internally and externally as needed.
  • Ensure accuracy of data in the Clinical Trial Management System (CTMS) and associated clinical trial monitoring systems
  • Conduct quality review and maintain inventory of study status throughout the study activation process
  • Implement quality measures in the CTMS to document and track pipeline trials
  • Compile activation metrics and reports for use by senior management and cancer center leadership
  • Work directly with key stakeholders and senior management to examine opportunities for decreasing study time to activation and promote the use of novel approaches across CRMO units to resolve issues and problems
  • Develop and lead LCCC's educational effort regarding time to study activation.
  • As needed, coordinate or assist in the issuance and maintenance of NCI National Clinical Trial Network membership and ensure appropriate user access to protocol information
  • Actively participate in meetings, task forces, and committees as assigned


Qualifications
  • Bachelor's degree in a scientific or health related field
  • 3 to 5 years of related experience
  • Knowledge of clinical research, research processes, and Good Clinical Practice (GCP)
  • Excellent verbal and written communication skills
  • Excellent organizational skills and attention to detail
  • Reliability and skilled in prioritizing competing responsibilities


Preferred qualification

Strong working knowledge of FDA, NCI, OHRP, and ICH requirements

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/Study-Activation-Coordinator-for-Clinical-Research-Management-Office--Lombardi-Comprehensive-Cancer-Center---Georgetown-University-Medical-Center--GUMC-_JR10351





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Job No:
Posted: 6/7/2021
Application Due: 6/7/2033
Work Type: Full Time
Salary: