Medical Director Oncologist

Clario

4d•Remote

About The Position

As a Medical Director at Clario, you will bring your oncology and clinical expertise to support high‑quality imaging and clinical trial delivery. In this role, you will interpret clinical data, ensure medical rigor across oncology studies, and collaborate with cross‑functional teams to meet sponsor expectations and uphold Clario’s standards of scientific and operational excellence.

Requirements

Medical degree.
Valid US medical license preferred.
Graduate of an approved oncology program; Board‑Certified Oncologist.
Experience in research and/or imaging core labs preferred.
Strong understanding of treatment response evaluation for solid tumors and hematologic malignancies.
Ability to manage multiple projects with strong organizational and time‑management skills.
Self‑motivated, flexible, and adaptable to changing business needs.
Strong interpersonal skills with a professional, collaborative approach.
Analytical abilities in diagnosis, radiographic assessment, and oncology treatment interpretation.
Ability to work extended periods at a computer; minimal lifting (0–10 lbs); minimal travel (0–5%).

Responsibilities

Interpreting clinical data according to medical standards, GCP guidelines, study protocols, charter definitions, and Clario SOPs.
Completing source documents accurately and promptly per protocol and SOP requirements.
Correcting entries on source documents and Case Report Forms (CRFs) in a timely manner.
Participating in protocol‑specific and ongoing training.
Performing Photo Image Quality Assessment (Photo IQA) and participating in the medical photography process.
Reviewing protocols, charters, and associated clinical and technical documents.
Maintaining security and confidentiality of images, data, equipment, study materials, and subject information.
Participating in sponsor site visits and audits as needed.
Collaborating with management to address and resolve oncology‑related study concerns.
Maintaining continuing professional medical education.
Conducting quality control to ensure completeness and accuracy of assigned work.
Identifying and supporting performance improvement initiatives.
Contributing to the development, review, and evaluation of SOPs and study‑specific procedures.
Creating oncology‑specific test cases for training.
Maintaining a safe work environment and promptly reporting hazards.
Participating in the Medical Affairs lecture series.
Performing other duties as assigned by Medical Affairs leadership.
Reading, understanding, and adhering to organizational SOPs.
Supporting the establishment and enforcement of departmental standards.
Participating in user acceptance testing for new tools and software enhancements.
Assisting in updates to departmental SOPs.
Exploring opportunities to improve departmental and organizational processes.
Collaborating with internal and external teams to resolve image quality issues, data discrepancies, and related concerns.
Attending project‑specific, system, and team trainings.
Training colleagues on imaging modalities and system applications, including proprietary and third-party tools.
Performing additional duties as assigned.