Clinical Project Manager

Posted 1ds ago

Employment Information

Education
Salary
Experience
Job Type

Report this job

Job expired or something wrong with this job?

Job Description

Clinical Project Manager overseeing pharmaceutical, biotechnology, and CRO research studies for Alira Health. Leading sponsors, clinical teams, compliance, budgets, and trial milestones.

Responsibilities:

  • 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 Project Managers
  • Create and review clinical study documents, protocols, ICF templates, study budgets, site logs/forms, study manuals and plans, and site binders
  • Drive 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 as required
  • Perform additional duties as assigned

Requirements:

  • BS/BA from an undergraduate program (life sciences or related discipline preferred) or equivalent experience
  • 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 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