Senior Project Manager

🔥 1 hour ago

🍂 Massachusetts – Remote

🍂 Massachusetts – Remote

💵 $140k - $150k / year

⏰ Full Time

🟠 Senior

👷‍♀️ Project Manager

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

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

• Manage clinical research studies according to approved scope of work/budget, ICH GCP guidelines, FDA regulations, and established timelines • Serve as study lead and primary contact for sponsors • Manage clinical study functions including investigational supply, IWRS/IXRS, data management, biostatistics, pharmacovigilance, and central laboratory • Generate and present study status updates and reports to sponsors • Supervise and support Clinical Assistants, In-house Clinical Research Associates, and Clinical Research Associates • Supervise and train Associate CPMs and provide guidance to CPMs • Create and review clinical study documents, protocols, ICF templates, budgets, site logs/forms, study manuals and plans, and site binders • Facilitate clinical teamwork and communications to achieve trial milestones • Ensure accuracy of reports and work products • Provide monthly billing information to the finance team • Present at investigator meetings and new client meetings • Update management through frequent communication • Identify issues and develop problem-solving strategies to meet study timelines • Manage subject accrual, retention, and compliance • Assist with TMF management and manage TMF reviews as needed • Prepare for and participate in third-party audits and FDA inspections • Ensure compliance with ICH GCP guidelines, FDA regulations, and company SOPs • Participate in internal, client/sponsor, scientific, and other meetings • Perform additional duties as assigned

🎯 Requirements

• BS/BA from an undergraduate program (life sciences or related discipline preferred) or equivalent experience • 10 years of experience in the pharmaceutical / biotechnology / CRO industry with at least 5 years of clinical project management experience • Proven ability to be careful, thorough, and detail-oriented • Strong organizational skills and 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 • Permanent authorization to work in the U.S. • Bachelor of Science in Biology, Biotechnology, Life Sciences, or Pharmacy