Associate Research, Oncology

About the Role

As an Assoc-Research-Clinical, you will play a vital role in the design, administration, and monitoring of clinical trials. Your work will directly support research teams, investigators, and patients by ensuring the integrity and success of clinical studies. This role is essential in advancing medical knowledge and improving healthcare delivery.

Key Responsibilities

• Plan, organize, perform, and monitor daily project protocols.
• Collect, prepare, and maintain essential research documentation, including informed consent records, case records, clinical notes, and medical reports.
• Report and assist with managing protocol deviations, adverse events, and other project-related issues.
• Assist with preparing and delivering internal and external presentations, conference reports, lectures, and publishing submissions.

Requirements & Tech Stack

• Understanding of the Food and Drug Administration (FDA) rules is beneficial.

Qualifications

• None specified.