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Salary
≈ $7.5k – $14k per year (Estimated)
Location
Remote (India)
Seniority
Junior · 1+ year exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 10, 2026. First seen by Alion on Oct 9, 2026. Clario scores A on the Alion truth index.

Overview
Company
Impact
Profile match
Clario is a healthcare technology company headquartered in Philadelphia, Pennsylvania, with a history dating back to 1972. The organization provides clinical trial endpoint technology and services, including electronic clinical outcome assessments, medical imaging, cardiac safety monitoring, and respiratory solutions. It operates on a global scale, supporting pharmaceutical and biotechnology firms through all phases of clinical research to generate high-quality evidence for regulatory submissions.

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.

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