Medical Oncologist

Clario

5d

About The Position

Clario, a part of Thermo Fisher Scientific, is seeking a Medical Oncologist to support oncology-focused clinical research through expert medical review, data interpretation, and quality oversight across imaging and clinical endpoints. The role collaborates with internal teams, sponsors, and regulatory stakeholders to help ensure oncology deliverables are high-quality, compliant, and scientifically sound.

The Medical Oncologist interprets clinical data in accordance with standard medical practice, Good Clinical Practice guidelines, study protocols, charters, and Clario SOPs. The role also reviews study documentation, supports medical photography and image quality assessment, performs quality checks, and contributes to training, continuous improvement, and the development of procedures. The position requires maintaining medical competency and protecting the confidentiality and integrity of study data and subject information.

Requirements

• Medical degree (MD or equivalent).
• 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, including the ability to manage multiple projects concurrently.
• Self-motivated, flexible, and adaptable to evolving business needs.
• Strong interpersonal and communication skills and a professional, collaborative demeanor.
• Analytical skills to interpret diagnoses, radiographic assessments, and oncology treatment outcomes effectively.

Nice To Haves

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

Responsibilities

• Interpret clinical data in accordance with standard medical practice, GCP guidelines, study protocols, charters, and Clario SOPs.
• Complete source documents and Case Report Forms (CRFs) accurately and on time, in accordance with protocol and charter requirements.
• Correct documentation entries as required while 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 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 promptly report workplace hazards.
• Perform additional duties as assigned by the Chief Medical Officer, VP of Medical Oncology, or Senior Medical Director.

Benefits

• Competitive compensation aligned to the U.S. market.
• Comprehensive health, retirement, and wellness benefits.
• Opportunities to work on global oncology clinical trials.
• Collaboration with multidisciplinary medical, scientific, and operational teams.
• Ongoing professional development and continuing medical education support.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree