Project Manager

🕒 July 3

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Alira Health

WebsiteLinkedInAll Job Openings

501 - 1000 employees

🏥 Healthcare

🏭 Manufacturing

⚕️ Healthcare Insurance

💰 $58M Venture Round on 2023-01

Healthcare • Manufacturing • Healthcare Insurance

Alira Health is a global consulting firm that partners with life sciences companies to develop innovative solutions in healthcare. The company specializes in a wide range of services including research and clinical development, regulatory compliance, and management consulting. Alira Health focuses on patient engagement, market access, and providing real-world solutions to improve patient outcomes. They are committed to environmental sustainability and actively participate in community involvement and ESG initiatives. Alira Health also provides technology solutions with a focus on improving life sciences research through empathy and scientific excellence.

📋 Description

• Manages clinical research studies to ensure studies are conducted in accordance with approved scope of work/budget, ICH GCP guidelines, and FDA regulations and within established timelines • Serves as study lead and primary contact for sponsors • Manages clinical study functions, which may include investigational supply, IWRS/IXRS, data management, biostatistics, pharmacovigilance, and central laboratory • Generates and presents frequent study status updates and reports to sponsor • Supervises and provides support to the Clinical team, including Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates • Supervises and trains Associate PMs • Creates and reviews clinical study documents, including protocols, ICF templates, study budgets, site log/form templates, study manuals and plans, site binders, etc • Drives and facilitates clinical teamwork and communications to ensure timely attainment of trial milestones • Ensures accuracy of reports and material work product • Provides monthly billing information to finance team • Presents at project meetings such as investigator meetings and new client meetings • Updates management accurately and regularly through frequent communication • Identifies issues and develops problem-solving strategies to ensure study timelines are met • Manages subject accrual, retention, and compliance • Assists in TMF management and manages TMF reviews as needed • Prepares for and participates in third-party audits and FDA inspections • Complies with and ensures team compliance with ICH GCP guidelines, FDA regulations, and company SOPs • Participates in internal, client/sponsor, scientific, and other meetings as required • Performs additional duties as assigned

🎯 Requirements

• BS/BA from an undergraduate program (life sciences or related discipline preferred) • 3 years of experience in the pharmaceutical / biotechnology / CRO industry with 1 year of management experience • Proven ability to be careful, thorough, and detail-oriented • Strong organizational skills and the ability to multi-task and work effectively in a fast-paced environment • Strong analytical, negotiation, meeting management, cross-functional team, and leadership skills • Self-starter who thrives in a collaborative, yet less structured team environment • Ability to problem-solve unstructured or ambiguous challenges • Strong command of English, both written and verbal • Excellent communication and interpersonal skills with customer service orientation • Proficient with MS Office Suite, particularly Word and Excel

🏖️ Benefits

• Professional development • Global travel • Flexible work programs