About the RoleWe are seeking a detail-oriented and proactive Project Manager with pharmaceutical industry experience to support cross-functional projects across regulatory, clinical, supply chain, R&D, and IT domains. The ideal candidate will assist in project planning, documentation, stakeholder communication, and status reporting, ensuring alignment with project goals and regulatory compliance requirements (GxP, FDA, EMA).ResponsibilitiesCoordinate and track project timelines, deliverables, and milestones across cross-functional teams.Work closely with project managers, clinical teams, regulatory affairs, and other departments to ensure projects meet deadlines and compliance standards.Maintain project documentation including meeting minutes, action items, risk logs, and change requests.Support in preparation of project reports, presentations, and stakeholder updates.Assist in resource planning, budgeting, and procurement activities as required.Schedule and facilitate team meetings, reviews, and vendor coordination calls.Ensure compliance with GxP, FDA, and other regulatory standards throughout project execution.Use project management tools (like MS Project, JIRA, Smartsheet, etc.) for tracking and reporting.Liaise with external partners, CROs, CMOs, or vendors as needed.QualificationsBachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Business Administration, or a related field.Required SkillsStrong project management skills.Excellent communication and interpersonal skills.Proficiency in project management tools.Ability to work collaboratively in a team environment.Preferred SkillsExperience in the pharmaceutical industry.Knowledge of regulatory compliance standards (GxP, FDA, EMA).Familiarity with budgeting and resource planning.Pay range and compensation packageOverall 8+ years required.Equal Opportunity StatementWe are committed to diversity and inclusivity in our hiring practices and encourage applications from all qualified individuals.
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