Project Manager, Respiratory

Clario; Bengaluru; Hybrid; INR 1,200,000 - 2,000,000; Full time

Benefits offered by this job

Competitive pay

Provident fund & medical insurance

Employee programs & events

Remote work flexibility

Career growth opportunities

Job summary

Clario is seeking a Project Manager to lead respiratory clinical studies from planning to closeout. You will serve as the primary liaison between clients and cross-functional teams, ensuring timelines, budgets, and quality requirements are met.

The role emphasizes operational excellence and customer satisfaction within a global organization. The position offers flexible remote work options and opportunities for professional development.

Qualifications

• Bachelor's degree or equivalent in a related field.
• 1–4 years of project management experience in pharma, healthcare, clinical research, medical device, life sciences, or related industries.
• Strong understanding of drug development and clinical research environments.
• Excellent communication, planning, and prioritization skills.
• Experience coordinating multiple stakeholders, timelines, budgets and deliverables.

Responsibilities

• Lead planning, setup, monitoring, and closeout of respiratory clinical studies and programs.
• Translate client requirements into deliverables for internal teams.
• Develop and manage study documentation throughout the lifecycle.
• Coordinate distribution and tracking of study equipment and materials.
• Prepare and distribute study status reports and communications to clients.

Skills

Project management

Communication

Time management

Organizational skills

Stakeholder management

English proficiency

Education

Bachelor's degree or equivalent

Tools

Microsoft Office

Job description

Join Clario, a part of Thermo Fisher Scientific and help advance respiratory clinical research through the delivery of high-quality project management services. As a Project Manager within our Respiratory Solutions team, you will lead study execution from initial planning through closeout, serving as the primary point of coordination between clients and cross-functional teams. You will drive operational excellence, ensure customer satisfaction, manage study timelines and budgets, and support the successful delivery of respiratory clinical trial technologies and services. This role offers the opportunity to build strong client relationships while contributing to the development of innovative solutions that help bring life-changing therapies to patients faster.

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
• Opportunities for professional development and career growth within a global organization

What You'll Be Doing

• Lead the planning, setup, monitoring, and closeout phases of respiratory clinical studies and programs.
• Gather customer requirements and translate project needs into actionable deliverables for internal operational teams.
• Develop, maintain, and manage study documentation throughout the project lifecycle.
• Coordinate the distribution, tracking, and reconciliation of study equipment and related materials.
• Create, review, and distribute study status reports and project communications to clients and stakeholders.
• Ensure appropriate archiving of study data, documentation, and project records in accordance with company and regulatory requirements.
• Establish, manage, and fulfill customer expectations through proactive communication and stakeholder engagement.
• Monitor study timelines, deliverables, and milestones to ensure successful on-time project execution.
• Manage financial aspects of assigned studies, including budget reviews, revenue forecasting, scope change assessments, and invoice reconciliation activities.
• Identify project risks, develop mitigation plans, and elevate issues appropriately to support study success.
• Facilitate collaboration between clients, vendors, and internal teams to ensure effective communication and efficient resource utilization.
• Lead internal and external discussions and negotiations to support study objectives and contractual commitments.
• Apply structured problem-solving techniques to address client concerns, resolve operational challenges, and maintain issue tracking documentation.
• Ensure timely resolution of customer escalations while maintaining a high level of client satisfaction.
• Support business development, operational, investigator, and site meetings by presenting project services, operational workflows, and study updates when required.
• Assist with onboarding, mentoring, and training of new project management team members.
• Participate in departmental initiatives, special projects, and continuous improvement activities.

What We Look For

• Bachelor's degree or equivalent combination of education and relevant project management experience.
• 1 to 4 years of project management experience within the pharmaceutical, healthcare, clinical research, medical device, life sciences, or related industries.
• Understanding of the drug development process and clinical research environment.
• Strong project planning, organizational, time management, and prioritization skills.
• Experience coordinating multiple stakeholders, timelines, budgets, and deliverables simultaneously.
• Knowledge of project financial management, including budgeting, forecasting, invoicing, and scope management principles.
• Ability to identify project risks and implement effective mitigation strategies.
• Outstanding verbal and written communication skills with the ability to communicate effectively in English.
• Strong interpersonal skills with the ability to build productive patient and cross-functional team relationships.
• Proficiency with Microsoft Office applications, including Excel, PowerPoint, Word, Outlook, and Teams.
• High attention to detail and demonstrated responsiveness to customer inquiries and operational requests.
• Ability to work independently, manage competing priorities, and perform effectively in a fast-paced 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, and 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.