Clario
Clinical Project Manager
Remote, IN
Role snapshot
Clario is hiring a Clinical Project Manager on a full-time basis. This is a remote role open to candidates in IN. The listing highlights Clinical Project Manager, Clinical Trial Project Manager and Clinical Research Project Manager.
- Company
- Clario
- Location
- Remote, IN
- Work mode
- Remote
- Job type
- Full-time
- Experience
- 1–3 years
- Posted
- Nov 14, 2026
Who this role suits
People with roughly one to three years of experience who can own small pieces of work with light guidance and want to widen their scope.
How to prepare your application
- Check your résumé against the listed skills (Clinical Project Manager, Clinical Trial Project Manager and Clinical Research Project Manager) and give each one a concrete example: what you built or achieved, not just that you used it.
- Prepare two or three stories about work you owned end to end, including one thing that went wrong and what you changed.
- Read what Clario publishes about its product or team, so you can say clearly why this role and this company.
- For remote roles, show that you communicate clearly in writing and can work without close supervision.
Apply only on Clario's own site. A genuine employer never asks candidates for money, deposits or bank details to apply, interview or “secure” a job. If something looks wrong, use Report a problem with this listing and we will review it. Read how we check listings.
About the role
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.
Originally posted on Himalayas