Medical & Scientific Affairs Advisor

Clario

2d•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.

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).

Nice To Haves

medical imaging software experience preferred.

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.