Project Manager - Cardiac Safety
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What you'll do
- 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 they're looking 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%
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
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.
Company
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