Medical & Scientific Affairs Advisor

Clario

1d•Remote

About The Position

At Clario, part of Thermo Fisher Scientific, we develop regulated technology that helps unlock better evidence and improve patient outcomes worldwide. Our software platforms support clinical trials, diagnostics, and medical decision-making in highly controlled regulatory environments. As a Medical & Scientific Affairs Advisor, you will serve as a scientific and imaging expert, partnering across functions to support high‑quality independent image review, regulatory readiness, and innovation in clinical research, helping bring life‑changing therapies to patients faster. What We Offer Competitive compensation Comprehensive health, dental, and vision coverage Retirement savings plan with company contribution Paid time off and company holidays Flexible work arrangements (role dependent) What You’ll Be Doing Serve as an imaging advisor supporting company operations and initiatives across assigned therapeutic areas. Provide scientific input on clinical trial design, image review methodology, and image data quality control. Manage and enhance processes for independent image review, ensuring consistency, quality, and regulatory readiness. Monitor, review, and communicate industry trends related to independent review to maintain service leadership. Implement training standards for new radiologists, study‑specific needs, and emerging imaging criteria. Contribute to scientific publications, abstracts, editorials, and thought leadership initiatives. Identify and implement innovations to improve central read efficiency and interpretation techniques. Create, review, and maintain imaging documentation, including charters, imaging manuals, and study-specific rules. Develop operational strategies for new imaging criteria and modalities, including nuclear medicine (e.g., PET/CT). Support radiopharmaceutical trials, specialized client requests, CMO review processes, sponsor audits, and regulatory inspections. Partner with application development and business development teams to translate scientific requirements into operational and client-facing solutions. Lead, mentor, and develop team members through training, coaching, and performance guidance. What We Look For Bachelor’s degree required; advanced degree preferred, or equivalent practical experience. 5+ years of experience in clinical trials and/or the pharmaceutical environment. Demonstrated expertise in multi‑modality imaging projects; medical imaging software experience preferred. Strong understanding of imaging criteria, clinical trial operations, and regulatory expectations. Proven ability to lead, mentor, and collaborate across multidisciplinary teams. Excellent written and verbal communication skills with strong organizational and analytical capabilities. Ability to work independently and adapt to changing priorities in a fast‑paced environment. Based in, or able to work from, the United States (remote). 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. Clario is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. 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.

Requirements

Bachelor’s degree required; advanced degree preferred, or equivalent practical experience.
5+ years of experience in clinical trials and/or the pharmaceutical environment.
Demonstrated expertise in multi‑modality imaging projects; medical imaging software experience preferred.
Strong understanding of imaging criteria, clinical trial operations, and regulatory expectations.
Proven ability to lead, mentor, and collaborate across multidisciplinary teams.
Excellent written and verbal communication skills with strong organizational and analytical capabilities.
Ability to work independently and adapt to changing priorities in a fast‑paced environment.
Based in, or able to work from, the United States (remote).

Responsibilities

Serve as an imaging advisor supporting company operations and initiatives across assigned therapeutic areas.
Provide scientific input on clinical trial design, image review methodology, and image data quality control.
Manage and enhance processes for independent image review, ensuring consistency, quality, and regulatory readiness.
Monitor, review, and communicate industry trends related to independent review to maintain service leadership.
Implement training standards for new radiologists, study‑specific needs, and emerging imaging criteria.
Contribute to scientific publications, abstracts, editorials, and thought leadership initiatives.
Identify and implement innovations to improve central read efficiency and interpretation techniques.
Create, review, and maintain imaging documentation, including charters, imaging manuals, and study-specific rules.
Develop operational strategies for new imaging criteria and modalities, including nuclear medicine (e.g., PET/CT).
Support radiopharmaceutical trials, specialized client requests, CMO review processes, sponsor audits, and regulatory inspections.
Partner with application development and business development teams to translate scientific requirements into operational and client-facing solutions.
Lead, mentor, and develop team members through training, coaching, and performance guidance.