Join Clario, a part of Thermo Fisher Scientific and help deliver innovative Digital Physiology solutions that support clinical trials worldwide. As a Project Coordinator, you will play a critical role in supporting study execution from startup through closeout, working closely with Project Managers, sponsors, sites, and cross-functional teams to ensure projects are delivered on time, within scope, and with exceptional quality. This role offers an excellent opportunity to develop project management expertise within a fast-paced clinical research environment while contributing to technologies that help bring life-changing therapies to patients faster.
What We Offer
- Competitive pay and incentives.
- Provident fund and medical insurance.
- Engaging employee programs and local events.
- Modern office spaces and remote work flexibility.
What You'll Be Doing
- Support Project Managers throughout the planning, setup, monitoring, and closeout phases of Digital Physiology studies and programs.
- Assist with study database setup, maintenance, and project tracking activities.
- Prepare, maintain, and organize study documentation and project records throughout the study lifecycle.
- Coordinate device and equipment distribution, inventory tracking, reconciliation, and logistics activities.
- Create, update, and distribute project reports, status updates, meeting materials, and study communications.
- Support the archival of study documentation and records in accordance with company procedures and regulatory requirements.
- Coordinate Project Assurance meetings, prepare agendas, document meeting minutes, and track action items through completion.
- Assist with documentation and database updates resulting from scope changes and project modifications.
- Support financial activities, including invoice reconciliation follow-up and preparation of forecasting and project reports.
- Facilitate issue management by documenting, tracking, and monitoring project issues to support timely resolution of customer concerns and escalations.
- Monitor project timelines and deliverables to help ensure study milestones are achieved.
- Respond to customer inquiries and participate in sponsor meetings and project calls as requested by the Project Manager.
- Take ownership of assigned project activities and independently manage specific deliverables when appropriate.
- Ensure timely completion of required training, documentation, and compliance requirements.
- Support continuous improvement initiatives and contribute to departmental objectives and operational excellence.
What We Look For
- Bachelor's degree preferred, or equivalent combination of education and relevant industry experience.
- 1 to 3 years of experience within pharmaceutical, biotechnology, healthcare, clinical research, life sciences, Digital Physiology, or related industries.
- Understanding of the drug development process and clinical trial environment.
- Strong organizational, planning, prioritization, and multitasking skills.
- Excellent interpersonal and relationship-building skills with the ability to collaborate effectively across functions and geographies.
- Strong verbal and written communication skills, including the ability to communicate effectively in English.
- Proficiency with Microsoft Office applications, including Excel, Word, PowerPoint, Outlook, and Teams.
- High attention to detail with demonstrated responsiveness to inquiries, requests, and project deadlines.
- Strong time-management skills and the ability to manage competing priorities in a fast-paced environment.
- Customer-focused mindset with a commitment to delivering high-quality service and operational support.
- Ability to work independently while contributing effectively within a collaborative global team environment.
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. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.
Skills Required
- Bachelor's degree or equivalent combination of education and relevant industry experience
- 1 to 3 years of experience in pharmaceutical, biotechnology, healthcare, clinical research, life sciences, Digital Physiology, or a related industry
- Understanding of the drug development process and clinical trial environment
- Proficiency with Microsoft Office applications, including Excel, Word, PowerPoint, Outlook, and Teams
- Strong organizational, planning, prioritization, and multitasking skills
- Strong verbal and written communication skills in English
- Ability to collaborate effectively across functions and geographies
- High attention to detail and responsiveness to inquiries, requests, and deadlines
- Strong time-management skills and ability to manage competing priorities
- Ability to work independently within a collaborative global team
Clario Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Clario and has not been reviewed or approved by Clario.
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Leave & Time Off Breadth — Time off is described as generous, including flexible PTO for some roles and up to 26–31 PTO days for eligible staff. The calendar includes 15 paid company holidays and a Winter Break.
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Healthcare Strength — Healthcare offerings include multiple medical plan options via Highmark with coordinated care navigation, plus dental and vision through established carriers. Employer HSA contributions and mental-health support broaden the package.
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Inclusive Benefits Coverage — Coverage highlights include domestic-partner eligibility, transgender-inclusive care, and HIV prevention/treatment. These inclusive elements are presented alongside broader inclusion commitments.
Clario Insights
What We Do
-- Clario has been named a Top Workplace by Energage for the 2022 Top Workplaces USA national awards. -- Clario generates the richest clinical evidence by fusing our deep scientific expertise and global scale into the broadest endpoint technology platform. By doing this, we empower our partners to transform lives. With almost 50 years of experience, 19,000 clinical trials, and 870 regulatory approvals, Clario has mastered the ability to generate rich evidence across a Trial Anywhere™ portfolio: decentralized (DCT), hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe, and Asia Pacific, Clario delivers the power of certainty. Partners ————— Clario brings the best of ERT and Bioclinica together to work alongside our partners to solve some of their biggest questions on topics such as: - eCOA vs. paper - Decentralized Clinical Trial (DCT) - Rescue a clinical trial - Broad endpoint technology: cardiac safety, imaging, respiratory And many more. People ———— We are so honoured to be named a 2022 Top Workplace by Energage. One of our leading values at Clario is People First Always. We help individuals build meaningful careers at Clario as they serve to help transform patients lives. Join us on this journey and check out our careers page: https://clario.com/careers/








