Clinical Project Manager

US Biomedical Systems India Pvt Ltd.; India; Hybrid; INR 900,000 - 1,500,000; Full time

Benefits offered by this job

Provident fund

Medical insurance

Remote work flexibility

Job summary

Clario, a part of Thermo Fisher Scientific, in India, seeks a Clinical Project Manager to lead clinical trial projects from start-up to closeout, coordinating sponsors, sites and cross-functional teams while ensuring quality, timelines and budget.

The role requires 1–3 years of clinical trials experience (CRO/pharma), GCP/ICH knowledge, and familiarity with medical imaging. Flexible remote work options are available, with modern offices and competitive compensation.

Qualifications

• Bachelor’s degree or equivalent in life sciences or healthcare (e.g., life sciences, pharmacy, nursing).
• 1–3 years clinical trials experience in CRO/pharma, preferably in project management.
• Experience supporting clinical development of investigational medicines.
• Knowledge of GCP and ICH guidelines and clinical research regulations.
• Medical imaging experience preferred.
• Experience with Word, Excel; MS Project preferred.
• Ability to lead complex clinical projects with timelines, budgets and multiple stakeholders.
• Strong written and verbal communication; collaborative approach.
• Ability to work with sponsors, sites and cross-functional teams in quality-focused clinical research.

Responsibilities

• Lead study start-up activities translating requirements into project plans and documentation.
• Manage project execution and stakeholder communications with sponsor reps, teams, sites, BD and leadership.
• Monitor critical project factors including resources, risks, data collection and delivery against expectations.
• Own financial activities including monthly billing, forecasting, amendments and pass-through costs.
• Maintain knowledge of contracts, study protocols and SOPs with QA for deviations and updates.
• Lead, train and support cross-functional project teams with coaching and development.
• Support Business Development through capabilities discussions and sponsor meetings.
• Coordinate study closeout and submission activities; ensure deliverables.
• Provide people-management support including coaching, hiring and onboarding where applicable.

Skills

Stakeholder management

Project leadership

Communication skills

GCP/ICH knowledge

Financial management

Cross-functional collaboration

MS Office tools

Medical imaging

Clinical trial experience

Education

Bachelor’s degree in life sciences/healthcare

Tools

Microsoft Word

Microsoft Excel

Microsoft Project

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, 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 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.