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Clario Hiring for Project Manager, Respiratory in Clinical Research

Published on

Bachelor’s degree

Bangalore, India

1-4 Years

Verified Job

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Clario is hiring for the role of Project Manager, Respiratory in Bangalore, India. This opportunity is part of the Clinical Research function and is suitable for candidates with project management experience in pharmaceutical, biotechnology, clinical research, healthcare, life sciences, or a related industry.

In this role, the selected candidate will support the delivery of respiratory clinical trials from startup through closeout, working with sponsors and cross-functional teams to ensure high-quality project execution on time and within budget.

Job Details

CompanyClario
PositionProject Manager, Respiratory
DepartmentClinical Research
LocationBangalore, India
Employment TypeFull time
QualificationBachelor’s Degree
Experience1-4 Years

Job Description

As a Project Manager within the Respiratory team, the candidate will be responsible for managing respiratory clinical studies across the project lifecycle. The role involves project leadership, financial oversight, risk management, customer communication, and coordination with internal and external stakeholders.

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The position requires a strong understanding of clinical trial delivery, the drug development process, and the ability to manage multiple priorities in a fast-paced environment.

Key Responsibilities

  • Lead the planning, setup, monitoring, and closeout phases of respiratory clinical studies.
  • Gather customer requirements and translate study needs into clear deliverables for internal teams.
  • Develop, maintain, and manage study documentation throughout the project lifecycle.
  • Coordinate the distribution, tracking, and reconciliation of study equipment and materials.
  • Create and distribute project reports, status updates, metrics, and customer communications.
  • Ensure study data and documentation are appropriately archived following project completion.
  • Establish and manage customer expectations through proactive communication and effective stakeholder management.
  • Monitor study timelines, milestones, deliverables, and dependencies to support on-time execution.
  • Manage project financials, including budget reviews, revenue forecasting, scope changes, and invoice reconciliation.
  • Identify project risks, develop mitigation strategies, and escalate issues appropriately.
  • Lead internal and external discussions and negotiations to meet study timelines and contractual commitments.
  • Apply structured problem-solving approaches to resolve operational challenges and customer escalations.
  • Maintain issue tracking documentation and drive timely follow-up through resolution.
  • Present respiratory study services at Investigator Meetings, site initiation meetings, and other customer discussions as required.
  • Partner with Business Development and Operations teams during client meetings to present services and operational workflows.
  • Support the onboarding and training of new Project Management team members.
  • Contribute to process improvements and special projects that strengthen quality, efficiency, and customer satisfaction.

Qualification

  • Bachelor’s degree preferred, or equivalent combination of education and relevant project management experience.
  • Understanding of the drug development process and clinical trial lifecycle.
  • Experience managing project timelines, budgets, scope, risks, and cross-functional deliverables.
  • Strong organizational, prioritization, and time-management skills.
  • Excellent interpersonal and stakeholder-management capabilities.
  • Strong verbal and written communication skills with the ability to communicate effectively in English.
  • Proficiency with Microsoft Office applications, including Excel, PowerPoint, Word, Outlook, and Teams.
  • Strong attention to detail with demonstrated responsiveness to customer and project needs.
  • Ability to manage multiple priorities and solve problems effectively in a fast-paced environment.

Experience

Candidates should have 1 to 4 years of project management experience within pharmaceutical, biotechnology, clinical research, healthcare, life sciences, or a related industry.

Benefits

  • Competitive pay and incentives.
  • Provident fund and medical insurance.
  • Engaging employee programs and local events.
  • Modern office spaces and remote work flexibility.

How to Apply

Interested candidates can apply online through the official application link below.

APPLICATION DETAILS

How to apply

Apply online

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