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Clinical Project Manager

Role overview

Summary

This role is for a Clinical Project Manager at Clario, focusing on the delivery of clinical trial projects in medical imaging. You will connect sponsors, sites, and cross-functional teams while ensuring quality and compliance throughout the project lifecycle.

Qualifications

  • Bachelor’s degree or equivalent practical experience in life sciences, pharmacy, nursing or another healthcare field.
  • 1–3 years of clinical trials experience within a contract research organization (CRO) or pharmaceutical research environment.
  • Working knowledge of Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines.
  • Preferred: Medical imaging experience.
  • Preferred: Experience with Microsoft Word and Excel; Microsoft Project experience.

Responsibilities

  • Lead clinical study start-up activities, translating study requirements into project plans and timelines.
  • Manage project execution and stakeholder communications, providing updates to various teams.
  • Monitor project success factors, resource requirements, risks, and overall delivery against expectations.
  • Own key financial activities, including monthly billing and forecasting.

Key facts

Hard skills

Other skills

  • Communication
  • Leadership
  • Team Management
  • Coaching
  • Time Management

About the company

Clario logo

Clario

  • Clinical Research (CRO)
  • XLarge
  • 1,001–5,000
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

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Job description

Join Clario, a part of Thermo Fisher Scientific, as a Clinical Project Manager supporting medical imaging programs in India. You will lead the delivery of clinical trial projects from study start-up through closeout, connecting sponsors, sites and cross-functional teams while maintaining quality, timelines, financial oversight and protocol compliance. This is an opportunity to combine clinical project leadership with work that helps bring life-changing therapies to patients faster.


What We Offer


  • Competitive compensation 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


  • Lead clinical study start-up activities, translating study requirements and response assessment criteria into project plans, timelines, milestones, communication plans and study documentation.
  • Manage project execution and stakeholder communications, providing timely updates to sponsor representatives, project teams, sites, Business Development and leadership.
  • Monitor critical project success factors, resource requirements, risks, data collection activities and overall delivery against agreed project expectations.
  • Own key financial activities, including monthly billing, forecasting, scope reviews, amendments, pass-through costs and the project information required to support revenue reporting.
  • Maintain strong knowledge of project contracts, study protocols and Standard Operating Procedures (SOPs), partnering with Quality Assurance to address deviations and communicate protocol updates.
  • Lead, train and support cross-functional project teams, establishing clear project expectations and partnering with functional leaders on coaching and development.
  • Support Business Development activities through capabilities discussions, sponsor meetings and polished Investigator Meeting presentations.
  • Coordinate study closeout and applicable submission activities, ensuring project deliverables are completed appropriately.
  • Where applicable, provide people-management support, including setting expectations, coaching, performance management, hiring and onboarding.

What We Look For


  • Bachelor’s degree or equivalent practical experience; education in life sciences, pharmacy, nursing or another healthcare field is highly desirable.
  • 1–3 years of clinical trials experience within a contract research organization (CRO) or pharmaceutical research environment, preferably in project management.
  • Previous project or management experience supporting the clinical development of investigational medicines.
  • Working knowledge of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines and relevant clinical research regulations.
  • Medical imaging experience is preferred.
  • Experience with common project and business productivity tools, including Microsoft Word and Excel; Microsoft Project experience is preferred.
  • Demonstrated ability to organize and lead complex clinical projects while managing timelines, financial activities and multiple stakeholders.
  • Strong written and verbal communication skills with a collaborative, professional approach.
  • Ability to work effectively with sponsors, investigative sites and cross-functional teams in a quality-focused clinical research environment.

At Clario, a part of Thermo Fisher Scientific, 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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