Strategic Project Management Professional for Prestige Biopharma
1 day ago
Prestige Biopharma Limited is a dynamic biotechnology company committed to delivering innovative solutions in the pharmaceutical industry.
Job Title: Strategic Project Management ProfessionalWe are seeking an experienced and skilled Strategic Project Management Professional to join our team. The ideal candidate will have a strong background in project management, with expertise in overseeing complex projects from planning to execution.
Job Description:Project SupportThe successful candidate will be responsible for providing strategic support to project management activities, including planning, timeline monitoring, and budget tracking. This involves ensuring timely completion of projects for regulatory submissions and maintaining effective communication with internal and external stakeholders.
Project MonitoringYou will track and report project status, ensuring deadlines are met for ongoing projects and providing expert CMC support while monitoring CMO/CDMO activities. Additionally, you will facilitate the collection of information from both internal and external stakeholders in a timely manner.
Documentation ManagementEffective documentation management is crucial in this role. You will manage and maintain project documentation, including protocols, reports, SOPs, and meeting minutes. Your ability to coordinate the collection of information from various sources will ensure seamless project execution.
Stakeholder ManagementIn this position, you will play a key role in coordinating external collaborations, including managing agreements and overseeing the quality of deliverables. You will also monitor activities of CMOs, CDMOs, and other partners to ensure alignment with our company goals.
Sample and Logistics CoordinationYour responsibilities will extend to handling project logistics, including sample shipment and drug sourcing. You must be able to multitask and adapt quickly to dynamic changes in the project scope.
Regulatory SupportAs a Strategic Project Management Professional, you will assist in drafting the Quality Section of dossiers for clinical trial and marketing authorization applications. This requires ensuring alignment with regulatory requirements and agency expectations.
CMC SupportOffering strategic guidance to technical teams on CMC regulatory requirements and engaging in negotiations to resolve CMC-related issues is a critical aspect of this role. Your knowledge of the drug development process and technical/scientific knowledge will be invaluable in this position.
Requirements:Education- MSc or BSc in life science/chemistry
- Experience with office management software like MS Office (MS Excel, MS Word, MS PowerPoint) and other project management software
- Strong management and organization skills, attention to details, good written and verbal communication skills
- Superior time-management skill, able to multitask and quickly adapt to dynamic changes
We offer a competitive salary range of $80,000 - $110,000 per annum, depending on experience. In addition to your base salary, you can expect a comprehensive benefits package that includes health insurance, retirement savings plan, and paid time off.
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