Medical Oncologist

Clario

4d•Remote

About The Position

Clario, a part of Thermo Fisher Scientific, is a leading provider of endpoint technology solutions for clinical trials. We are seeking a Medical Oncologist to support oncology‑focused clinical research by providing expert medical review, data interpretation, and quality oversight across imaging and clinical endpoints. This role collaborates closely with internal teams, sponsors, and regulatory stakeholders to ensure high‑quality, compliant, and scientifically sound oncology deliverables.

Requirements

Medical degree (MD or equivalent) required
Board‑Certified Oncologist
Graduate of an approved oncology training program; subspecialty training as applicable
Comprehensive understanding of treatment response evaluation for solid tumors and hematologic malignancies
Strong organizational and time‑management skills with the ability to manage multiple projects concurrently
Self‑motivated, flexible, and adaptable to evolving business needs
Strong interpersonal and communication skills with a professional, collaborative demeanor
Analytical skills to effectively interpret diagnoses, radiographic assessments, and oncology treatment outcomes.

Nice To Haves

Valid U.S. medical license preferred
Experience in clinical research and/or imaging core lab environments preferred

Responsibilities

Interpret clinical data in accordance with standard medical practice, Good Clinical Practice (GCP) guidelines, study protocols, charters, and Clario SOPs
Accurately and timely complete source documents and Case Report Forms (CRFs) in line with protocol and charter requirements
Correct documentation entries as required, ensuring traceability and compliance
Participate in protocol‑specific training sessions and onboarding activities
Perform Photo Image Quality Assessment (Photo IQA) and participate in the medical photography process
Review study protocols, charters, and associated clinical and technical documentation
Ensure the security, confidentiality, and integrity of images, data, equipment, study protocols, and subject information
Participate in sponsor site visits, audits, and inspections as requested
Collaborate with management to identify, troubleshoot, and resolve oncology study issues
Maintain responsibility for ongoing professional education and medical competency
Perform quality control checks on assigned work for completeness and accuracy
Identify opportunities for and participate in continuous performance improvement initiatives
Contribute to the development, review, and evaluation of SOPs and study‑specific procedures
Create test cases and support oncology‑specific training initiatives
Participate in the Medical Affairs lecture series
Maintain a safe work environment and report workplace hazards promptly
Perform additional duties as assigned by the Chief Medical Officer, VP of Medical Oncology, or Senior Medical Director