Assistant Clinical Project Manager

Clario; India; Remote; INR 600,000 - 1,200,000; Full time

Benefits offered by this job

Competitive pay

Provident fund

Medical insurance

Employee programs

Local events

Remote work flexibility

Job summary

Clario is seeking an Assistant Clinical Project Manager in the Medical Imaging team to support study execution from startup through closeout. You will coordinate activities, manage documentation, monitor deliverables, and liaise with sponsors, sites, and internal teams to ensure on-time, within-scope delivery under GCP/ICH guidelines.

Ideal candidates have 1+ year in pharma/clinical operations, strong English communication, and proficiency in MS Office; remote work flexibility is offered.

Qualifications

• Associate's degree required; Bachelor's degree preferred.
• Experience coordinating clinical projects or trials is desirable.
• Strong written and verbal communication in English.
• Familiarity with regulatory requirements (GCP/ICH) preferred.

Responsibilities

• Support Clinical Project Managers with day-to-day project administration across imaging studies and programs.
• Develop and maintain project documentation, study materials, reports, and project records.
• Participate in project meetings and cross-functional discussions to drive milestones.
• Review study protocols to understand timelines and imaging deliverables.
• Create and distribute project reports for internal and external stakeholders.

Skills

Project coordination

Documentation

Stakeholder communication

English proficiency

MS Office

Education

Associate's degree

Bachelor's degree preferred

Tools

Microsoft Office

Job description

Join Clario, a part of Thermo Fisher Scientific and help deliver high-quality imaging services that support clinical trials around the world. As an Assistant Clinical Project Manager within our Medical Imaging team, you will play a key role in supporting study execution from startup through closeout. Working closely with Clinical Project Managers, sponsors, sites, and cross-functional teams, you will coordinate project activities, manage study documentation, monitor deliverables, and help ensure projects are delivered on time, within scope, and in accordance with applicable quality and regulatory requirements. This is an excellent opportunity to build project management expertise within a global clinical research environment while contributing to the development of life-changing therapies.

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 with day-to-day project administration across imaging studies and programs.
• Develop and maintain project documentation, study materials, presentations, reports, and project records.
• Participate in project meetings, sponsor calls, training sessions, and cross-functional discussions.
• Review and interpret study protocols to understand project requirements, timelines, and imaging deliverables.
• Serve as a liaison between internal teams to ensure timely completion of study milestones and project deliverables.
• Support project startup, execution, monitoring, and closeout activities throughout the study lifecycle.
• Assist with project financial activities, including scope change documentation updates, invoice reconciliation follow-up, and forecasting reports.
• Monitor internal workflows and data flow activities to support timely completion of operational tasks.
• Communicate professionally with clients, sponsors, sites, and internal stakeholders regarding project status and deliverables.
• Verify imaging protocol requirements are met and ensure study queries are appropriately identified and escalated.
• Create, review, and distribute project reports for internal and external stakeholders.
• Follow up on outstanding items, including missing data, incomplete documentation, site queries, and project action items.
• Support issue tracking and resolution by partnering with Clinical Project Managers and cross-functional teams.
• Assist with the management, distribution, and tracking of site-facing materials and logistics activities.
• Serve as an acting Project Manager when required and support continuity of project operations.
• Participate in process improvement initiatives and provide recommendations to enhance operational effectiveness.
• Perform project activities in accordance with Good Clinical Practice (GCP), ICH guidelines, FDA requirements, and company procedures.

What We Look For

• Associate's degree required; Bachelor's degree preferred.
• Minimum 1 year of experience in pharmaceutical drug development, clinical trials, clinical research, healthcare, or a related industry preferred.
• Experience supporting project teams, clinical operations, study management, or customer-facing activities is desirable.
• Understanding of clinical trial processes, medical imaging studies, or clinical research environments preferred.
• Strong proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, Outlook, and Teams.
• Excellent organizational, planning, prioritization, and time-management skills.
• Strong interpersonal and communication skills with the ability to communicate effectively in English.
• Exceptional attention to detail with a commitment to quality and accuracy.
• Ability to work independently while collaborating effectively across global cross-functional teams.
• Comfortable managing multiple priorities and adapting to changing business needs and timelines.
• Proactive, pragmatic, and goal-oriented approach to problem solving and project execution.
• Professional, customer-focused mindset with the ability to build productive relationships with sponsors, sites, and internal stakeholders.

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.

Clario Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.