Associate / Research Coordinator (DMOHS)

Roles & Responsibilities

The Division of Medical Oncology (DMO) is looking for a passionate and driven Associate / Research Coordinator to join their team! The selected candidate will assist investigators to conduct clinical research studies, ensuring that the studies are carried out and documented in accordance with the protocol, Good Clinical Practice (GCP) guidelines, all applicable regulatory requirements and Division of Medical Oncology (DMO) office’s standard operating procedures.

Main Responsibilities :

1. Conduct of Clinical Research Studies

• Assist the investigators in screening patients for clinical research and helping to take informed consent.
• Assist the investigators with patient’s assessment, data collection and questionnaires.
• Prepare documents required for monitoring by study monitors and help prepare study site for audit.
• Assist investigators to resolve data queries and discrepancies.

2. Administrative Duties

3. Maintaining Study Supplies and Investigator Site Files

4. Other Duties and Responsibilities

Requirements :

Tell employers what skills you have

Cancer Research

Informed Consent

Clinical Research

Clinical Research Administration

Highly self-motivated

Public Health

Healthcare

Oncology

Administration

patient recruitment

Data Entry

Clinical Trials

Protocol

Good Communication Skills

clinical trials protocols

Health Sciences

Life Sciences

Screening

Able To Work Independently

IRB