Clario

Project Manager - Cardiac Safety

Clario  •  United States (Remote)  •  12 days ago
Apply
AI can make mistakes so check important info. Chat history is never stored.

Job Description

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

About Clario

Clario is a leading healthcare research and technology company that generates high quality clinical evidence for our pharmaceutical, biotech, and medical device partners. We offer comprehensive evidence generation solutions that combine eCOA, cardiac safety, medical imaging, precision motion, and respiratory endpoints.

Since our founding more than 50 years ago, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported clinical trials over 26,000 times in more than 100 countries. Our global team of science, technology, and operational experts have supported over 60% of all FDA drug approvals since 2019.

For more information, visit Clario.com

Industry
Biotech & Life Sciences
Company Size
5,001-10,000 employees
Headquarters
Philadelphia, Pennsylvania
Year Founded
Unknown
Social Media