Hybrid Clinical Project Manager

Alira Health

Verona

Hybrid

EUR 50,000 - 70,000

Full time

11 days ago

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Job summary

Alira Health in Verona (hybrid) is seeking a Project Manager to lead one or more clinical study protocols, ensuring timelines, budgets, and regulatory compliance are met while coordinating with sponsors and vendors.

You will act as study lead for sponsors, supervise clinical team members, and drive documentation, TMF reviews, audits, and investigator meetings.

A BS/BA in life sciences and 3 years in pharma/CRO, plus strong English, MS Office skills, and a collaborative mindset, are required.

Qualifications

BS/BA from undergraduate program in life sciences or related field; 3 years pharma/CRO industry experience with 1 year in management.
Experience leading clinical studies including budgeting, timelines, and regulatory compliance.
Strong communication, organizational, and cross-functional collaboration skills.

Responsibilities

Manages clinical research studies to ensure adherence to scope, budget, and timelines.
Serves as study lead and primary contact for sponsors.
Oversees investigational supply, IWRS/IXRS, data management, biostatistics, pharmacovigilance, and lab activities.
Generates status reports and presents to sponsors.
Supervises Clinical team members and trains Associate PMs.
Prepares study documents, budgets, and site materials.
Drives team communication to meet trial milestones.
Ensures accuracy of reports and TMF reviews as needed.
Supports third-party audits and FDA inspections.