Clario

Compensation

Full Description

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. What We Offer Competitive compensation Medical, dental, and vision insurance beginning Day 1 of employment Flexible work schedules Attractive PTO plan Engaging employee programs Remote working What You’ll Be Doing 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. Secondary Responsibilities 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. What We Look For 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%). At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster. EEO Statement Clario is an equal opportunity employer. Clario evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic. Clario Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.