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Research Data Coordinator 1 - Clinical Research Management Office – Lombardi Comprehensive Cancer Center - Georgetown University Medical Center

Company

Georgetown University
Address , Washington, 20007, Dc
Employment type FULL_TIME
Salary
Expires 2023-06-25
Posted at 1 year ago
Job Description
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
Research Data Coordinator 1 - Clinical Research Management Office – Lombardi Comprehensive Cancer Center - Georgetown University Medical Center
The
Lombardi Comprehensive Cancer Center
, part of
Georgetown University Medical Center
, seeks to prevent, treat and cure cancers by linking scientific discovery, expert and compassionate patient care, quality education and partnership with the community guided by the principle of cura personalis – “care for the whole person.” Georgetown Lombardi is the research engine driving clinical cancer research at MedStar Health in the D.C. Metro area and northern New Jersey.
Job Overview
The Research Data Coordinator 1 is responsible for data management of varying complexity and disease indication for phase I, II, and III oncology clinical trials conducted within the Clinical Research Management Office (CRMO) of the Lombardi Comprehensive Cancer Center (LCCC). Duties include but are not limited to:
  • Ensures query resolution with proper physician and clinical study team oversight within site- and sponsor-specific time requirements
  • Collaborates closely with physicians and Study Coordinators to maintain protocol integrity
  • Ensures accuracy of data entered in the Clinical Trials Management System (CTMS) with patient information and key dates
  • Maintains confidentiality standards for all potential and enrolled study participants; and complies with federal Health Insurance Portability and Accountability Act (HIPAA) regulations
  • Attends protocol-related training and completes all required study training in the required timeframe
  • Supports all aspects of clinical research data management for clinical trials conducted in the LCCC Clinical Research Management Office (CRMO), including collection of data from source documents and medical records and completion of case report forms per sponsor requirements
  • Maintains controls to assure accuracy, completeness, and confidentiality of research data
  • Provides support during internal and external monitoring and auditing preparation, including supporting data deficiency corrections and development of corrective actions plans post-audit
  • Works collaboratively with trial stakeholders and internal study teams (physicians, Regulatory team, Study Coordinators, nursing staff, Research Laboratory Technicians, and Research Pharmacy team)
  • Communicates appropriately with pharmaceutical sponsors, study monitors, auditors, physicians, and study team members
  • Performs all duties in accordance with all applicable laws and regulations. Adheres to Georgetown University Medical Center’s philosophies, policies, and SOPs
  • Requests and uploads radiological images into sponsor-provided imaging platforms according to each study protocol
  • Interfaces with study team members to resolve discrepancies
  • Resolves imaging-related queries with the assistance of clinical study team
  • Works in compliance with Human Subject Protection regulations, patient confidentiality/HIPAA requirements, and Good Clinical Practice
  • Assures ongoing compliance with all departmental, institutional, and federal requirements and regulations
  • Reviews and analyzes information from medical records (clinic notes, pathology reports, radiology reports, patient questionnaires, etc.) to extract data for all assigned research protocols - including but not limited to industry, national, and investigator-initiated studies
  • Collects and organizes source documents in electronic and paper format according to site policies
  • Prepares for - and participates in - site initiation visits
  • Accurately captures data in electronic or paper Case Report Forms (eCRFs/CRFs), adhering to contractual timelines and site Standard Operating Procedures (SOPs)
  • Schedules sponsor monitoring and study close-out visits
Work Interactions
  • Clinical Research Manager
  • Clinical trial sponsors, auditors, and study monitors
  • Disease Group members: Principal Investigators, Physicians, Clinicians
  • External department clinicians and staff: Infusion Nurses, Oncology Pharmacists, hospital staff
  • Clinical Research Management Office (CRMO) members: Clinical Research Nurses, Clinical Research Coordinators, Data Coordinators, Regulatory Coordinators, Laboratory Technicians
Qualifications
  • High School diploma or equivalency
  • Reliability and ability to prioritize competing responsibilities
  • Ability to work independently and function within a team.
  • Strong attention to detail.
  • Up to 2 years of related experience
Work Mode: Hybrid. Please note that work mode designations are regularly reviewed in order to meet the evolving needs of the University. Such review may necessitate a change to a position’s mode of work designation. Complete details about Georgetown University’s mode of work designations for staff positions can be found on the Department of Human Resources
Mode of Work Designation
.
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 .
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 comprehensive and competitive benefit package that includes medical, dental, vision, disability and life insurance, retirement savings, tuition assistance, work-life balance benefits, employee discounts and an array of voluntary insurance options. You can learn more about benefits and eligibility on the
Department of Human Resources website
.