Logo for Clario

Assistant Clinical Project Manager

Role overview

Qualifications

  • 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
  • Strong proficiency with Microsoft Office applications, including Word, Excel, PowerPoint, Outlook, and Teams
  • Excellent organizational, planning, prioritization, and time-management skills

Responsibilities

  • 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
  • Monitor internal workflows and data flow activities to support timely completion of operational tasks

Key facts

Hard skills

Other skills

  • Microsoft Office
  • Time Management
  • Communication
  • Organizational Skills
  • Social Skills
  • Detail Oriented
  • Problem Solving

About the company

Clario logo

Clario

Contract Research Organizations (CRO)

Clario is a leading healthcare research and technology company that generates high quality clinical evidence for our pharmaceutical, biotech, and medical device partners. We offer comprehensive evidence generation solutions that combine eCOA, cardiac safety, medical imaging, precision motion, and respiratory endpoints. Since our founding more than 50 years ago, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported clinical trials over 26,000 times in more than 100 countries. Our global team of science, technology, and operational experts have supported over 60% of all FDA drug approvals since 2019. For more information, visit Clario.com

Company details

Company typeXLarge
IndustryContract Research Organizations (CRO)
Company size1001 - 5000

Your match analysis

See how your profile stacks up against this role.

We compared the job requirements to your profile to show where you're strong and where you fall short.

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.

Apply once. Then go straight to the hiring manager.

After you apply, unlock the direct contact details of the people who actually make the call. A quick follow-up makes you 5x more likely to land an interview.

MR

Marcus Rivera

Chief Revenue Officer

m.rivera@company.com
linkedin.com/in/marcusrivera
Unlocked after you apply
·

Project Manager Related jobs

Other jobs at Clario

Premium

Reach out to the hiring manager directly.

Gain access to the contact details of the hiring managers who actually decide, and reach out to network with them directly. That, plus more when you upgrade:

  • Full match report with fit score and gaps
  • Career diagnostics on how recruiters read you
  • Curated company matches and warm intros
  • 48h early access to new roles

Cancel anytime.