Project Manager - Cardiac Safety

At Clario, part of Thermo Fisher Scientific, we are transforming lives by unlocking better evidence through clinical trial technology and services. As a Project Manager, you will play a critical role in delivering high-quality study outcomes by ensuring projects are executed on time, within scope, and with exceptional client experience. This is an opportunity to collaborate cross‑functionally and contribute directly to advancing drug development programs. Join us and make an impact.

What You’ll Be Doing Lead the planning, setup, monitoring, and closeout phases of clinical study management, ensuring delivery of high-quality services Gather and translate customer requirements into actionable plans for internal teams Develop and maintain study documentation, reports, and data archiving processes Coordinate equipment distribution and tracking to support study execution Monitor study timelines and manage financial components, including budgets, revenue forecasting, scope changes, and invoice reconciliation Identify study risks, propose mitigation strategies, and escalate

issues as appropriate Manage internal and external stakeholder communications, negotiations, and relationships to ensure alignment and collaboration Promote a positive team environment through effective communication and resource coordination Apply structured problem-solving approaches to resolve client issues and maintain issue tracking for timely resolution Represent study services in client meetings, including investigator and site initiation meetings, as needed Support onboarding and training of new Project Management team members What We Look For Bachelor’s degree or equivalent

practical experience in project management or a related field 1–4 years of project management experience in the pharmaceutical, clinical, or related industry Knowledge of the drug development lifecycle and clinical trial processes Strong organizational, time management, and prioritization skills Excellent interpersonal and communication skills, with the ability to communicate effectively in English Proficiency in Microsoft Office applications Detail-oriented with demonstrated responsiveness and accountability Ability to manage multiple priorities in a fast-paced environment Valid passport

and willingness to travel up to approximately 20% At Clario, a part of Thermo Fisher Scientific, 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 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.

• Bachelor’s degree or equivalent experience in project management or related field with 1–4 years in pharmaceutical or clinical industry
• Knowledge of drug development lifecycle and clinical trial processes
• Strong organizational, communication skills, Microsoft Office proficiency, valid passport, and willingness to travel up to 20%