Assistant Clinical Project Manager
Clario, a part of Thermo Fisher Scientific, is the global leader in medical imaging, providing expert services and technology to support clinical trials across the drug development lifecycle. Within our industry‑leading Medical Imaging division, we support some of the most complex Oncology studies worldwide. We are currently seeking an Assistant Clinical Project Manager (ACPM) to support the successful delivery of imaging‑based clinical trials from our India operations.
This role offers exposure to global studies, cross‑functional collaboration, and the opportunity to build a strong foundation in clinical project management within a regulated, fast‑paced environment.
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 Clinical Project Managers (CPMs) with day‑to‑day project administration across study start‑up, execution, and close‑out activities
Develop, review, and edit project documentation, presentations, and reports
Read, understand, and apply clinical protocols and imaging requirements to project activities
Participate in project meetings, client calls, and internal training sessions
Act as a liaison across cross‑functional teams to ensure timely completion of study deliverables
Monitor internal data flow to ensure tasks are completed within agreed timelines
Track outstanding items such as missing data, queries, or incomplete documentation and follow up to resolution
Communicate project status updates to clients and internal stakeholders in a professional and timely manner
Support logistics activities, including distribution, tracking, and management of site‑facing materials
Assist with finance‑related activities such as scope change documentation, database updates, invoice reconciliation follow‑ups, and forecasting reports
Create, review, and distribute internal and external project reports
Serve as acting Project Manager during temporary CPM absence, as required
What We Look For
Associate’s degree required; Bachelor’s degree preferred
2+ years of experience in pharmaceutical drug development, clinical trials, or clinical research (preferred)
Strong working knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook)
Healthcare, medical imaging, or clinical research exposure preferred
Excellent written and verbal communication skills in English
Strong organizational, time management, and prioritization skills
Detail‑oriented, responsive, and able to manage multiple priorities
Ability to work independently while collaborating effectively in a team environment
Comfortable working in a dynamic, changing environment with a proactive and pragmatic approach
At Clario, 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.
This role offers exposure to global studies, cross‑functional collaboration, and the opportunity to build a strong foundation in clinical project management within a regulated, fast‑paced environment.
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 Clinical Project Managers (CPMs) with day‑to‑day project administration across study start‑up, execution, and close‑out activities
Develop, review, and edit project documentation, presentations, and reports
Read, understand, and apply clinical protocols and imaging requirements to project activities
Participate in project meetings, client calls, and internal training sessions
Act as a liaison across cross‑functional teams to ensure timely completion of study deliverables
Monitor internal data flow to ensure tasks are completed within agreed timelines
Track outstanding items such as missing data, queries, or incomplete documentation and follow up to resolution
Communicate project status updates to clients and internal stakeholders in a professional and timely manner
Support logistics activities, including distribution, tracking, and management of site‑facing materials
Assist with finance‑related activities such as scope change documentation, database updates, invoice reconciliation follow‑ups, and forecasting reports
Create, review, and distribute internal and external project reports
Serve as acting Project Manager during temporary CPM absence, as required
What We Look For
Associate’s degree required; Bachelor’s degree preferred
2+ years of experience in pharmaceutical drug development, clinical trials, or clinical research (preferred)
Strong working knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook)
Healthcare, medical imaging, or clinical research exposure preferred
Excellent written and verbal communication skills in English
Strong organizational, time management, and prioritization skills
Detail‑oriented, responsive, and able to manage multiple priorities
Ability to work independently while collaborating effectively in a team environment
Comfortable working in a dynamic, changing environment with a proactive and pragmatic approach
At Clario, 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.