Medical Oncologist
ExternalFull-timeRemote2w ago
Clinical TrialsComplianceDocumentationGCPSAFe
Prepare for this interview
EliteAI-generated questions, company research, and talking points tailored to this role
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
- What We Look For
- Medical degree (MD or equivalent) required
- Board‑Certified Oncologist
- Graduate of an approved oncology training program; subspecialty training as applicable
- Valid U.S. medical license preferred
- Experience in clinical research and/or imaging core lab environments preferred
- 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.
- Clario, a part of Thermo Fisher Scientific, is a leading provider of endpoint technology solutions for clinical trials, transforming lives by accelerating the development of therapies for patients worldwide.
- EEO Statement
Benefits
Competitive compensation aligned to the U.S. marketComprehensive health, retirement, and wellness benefitsOpportunities to work on global oncology clinical trialsCollaboration with multidisciplinary medical, scientific, and operational teamsOngoing professional development and continuing medical education supportHealth insuranceFlexible schedule
Additional Information
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.
Your Match
How well this role fits your profile.
Company Intel
What employees say
Worked at clarioclinical? Share your experience