Clinical Trials Coordinator

vor 1 Woche


Ingelheim am Rhein, Rheinland-Pfalz, Deutschland Georgetown University in Qatar Vollzeit
Job Summary

The Clinical Research Coordinator I serves as a key member of the research team at Georgetown University, responsible for the coordination and management of oncology clinical trials. This role requires strong organizational and communication skills, as well as the ability to work independently and as part of a team.

Key Responsibilities
  • Coordinate and manage the overall workflow of assigned clinical trials, ensuring timely completion of tasks and adherence to protocol requirements.
  • Collaborate with investigators and senior study team members to develop and implement study protocols, including recruitment and selection of study participants.
  • Interface with study participants to obtain and document informed consent, ensuring compliance with regulatory guidelines and institutional policies.
  • Coordinate and conduct study-related procedures and assessments, maintaining protocol integrity and patient safety.
  • Assist in the assessment, management, and coordination of patient care across the continuum of care, including triage of phone calls, symptom management, and proactive patient communication.
  • Coordinate the collection of research specimens and provide patient education on clinical trial participation, treatment, and potential side effects.
  • Schedule and conduct in-service training for staff on assigned clinical trials.
  • Update the Clinical Trials Management System (CTMS) with patient information and key dates to support responsible financial management of clinical trials.
  • Collaborate with Data Managers to ensure accurate and complete documentation for clinical trials, resolving queries in a timely manner.
  • Document and report serious adverse events per protocol and institutional policy.
  • Act as a liaison with hospital staff, physicians, IRB, review committees, clinical research finance team, and auditors.
Work Interactions

The Clinical Research Coordinator I reports directly to the Clinical Research Manager and works closely with Disease group members (Principal Investigators, Physicians, Clinicians). This position collaborates with the Clinical Research Management Office (CRMO) members (Clinical Research Nurses, Clinical Research Coordinators, Data Managers, Regulatory Coordinators, Laboratory Technicians). They also work with external department clinicians and staff (Infusion Nurses, Oncology Pharmacists, hospital staff) along with clinical trial sponsors, auditors, and study monitors.

Requirements and Qualifications
  • Bachelor's Degree in a scientific or health-related field.
  • Two (2) years of related experience in clinical research preferred.
  • Strong candidates exhibit the ability to work independently and function within a team, strong attention to detail, and is reliable and able to prioritize competing responsibilities.
Work Mode Designation

$44,642.00 USD Annual

Pay Range:

The projected salary or hourly pay range for this position which represents the full range of anticipated compensation is:

$44, $73,406.80

Compensation is determined by a number of factors including, but not limited to, the candidate's individual qualifications, experience, education, skills, and certifications, as well as the University's business needs and external factors.



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