Safety science and technology move forward here. So will you.
Prudentia, a PrimeVigilance company, is where safety science meets technology. We advise pharmaceutical companies on the processes and systems behind clinical and post-marketing safety, from selecting and implementing safety databases to managed services, data migration and turnkey tools that close the gaps in leading safety platforms.
It is specialist, high-trust work, and it depends on people who love solving hard problems. We are a team of curious minds, problem-solvers and experts brought together by a shared commitment to patient safety and to doing meaningful work well. Our culture values kindness, flexibility, growth and belonging, and we back one another to keep learning.
If you want a role with purpose, room to grow and the chance to make a real difference, we would love to hear from you.
Bridges the gap between individual project delivery and overarching program strategy, managing clusters of
related projects.
ADDITIONAL RESPONSIBILITIES
o Leads development of internal process docs (eg SOPs) and training materials
o Leads development of articles, brochures, whitepapers, POVs
o Identifies required PD activities
o Estimates budget for PD activities
• Additional Service offerings (SO)
o Well versed in 2+ SOs
o Leads small project or work stream
• Recruiting
o Identifies candidates from personal networks
o Assists with recruiting blitz as directed
o Conducts technical interviews
o Conduct culture / fit interview
o Author job description as directed
• Sales
o Represents company at bid defense
o Authors components of proposal
o Participates at conferences
o Identify new opportunities with existing clients
o Leads demos
• Admin
o Completes all admin tasks (e.g. time reporting, training records) timely with high quality
o Conduct appraisals for team members
o Review team T&E
Education
Bachelor's degree in pharmaceutical sciences, healthcare management, information technology, or a related field; PMP Certification preferred
Prudentia, a PrimeVigilance company, is where safety science meets technology. We advise pharmaceutical companies on the processes and systems behind clinical and post-marketing safety, from selecting and implementing safety databases to managed services, data migration and turnkey tools that close the gaps in leading safety platforms.
It is specialist, high-trust work, and it depends on people who love solving hard problems. We are a team of curious minds, problem-solvers and experts brought together by a shared commitment to patient safety and to doing meaningful work well. Our culture values kindness, flexibility, growth and belonging, and we back one another to keep learning.
If you want a role with purpose, room to grow and the chance to make a real difference, we would love to hear from you.
Bridges the gap between individual project delivery and overarching program strategy, managing clusters of
related projects.
ADDITIONAL RESPONSIBILITIES
o Leads development of internal process docs (eg SOPs) and training materials
o Leads development of articles, brochures, whitepapers, POVs
o Identifies required PD activities
o Estimates budget for PD activities
• Additional Service offerings (SO)
o Well versed in 2+ SOs
o Leads small project or work stream
• Recruiting
o Identifies candidates from personal networks
o Assists with recruiting blitz as directed
o Conducts technical interviews
o Conduct culture / fit interview
o Author job description as directed
• Sales
o Represents company at bid defense
o Authors components of proposal
o Participates at conferences
o Identify new opportunities with existing clients
o Leads demos
• Admin
o Completes all admin tasks (e.g. time reporting, training records) timely with high quality
o Conduct appraisals for team members
o Review team T&E
Education
Bachelor's degree in pharmaceutical sciences, healthcare management, information technology, or a related field; PMP Certification preferred
Responsibilities
Coordinate PMO activities as directed; Manage project scope, schedule, and costs; Maintain good client relations; Oversee task delivery and interim milestones.; Ensure assigned project tasks are delivered within budget and on time; Act as a secondary point of contact for clients.; Track risks/issues to closure; Status reporting to customer; Manage changes to project scope; Perform advanced financial analysis; Oversee Quality Management System activities for the client.; Coordinate inter-project dependencies; Consolidate reporting across multiple project streams; Manage project escalations.; Support Program Managers in strategic planning; Contribute to client governance meetings.; Practice Development (PD)Requirements
Ability to lead and motivate teams; Able to provide training to new hires and colleagues with good mentoring and coaching skills; Advanced resource allocation skills; Proactive approach to work with high level of commitment; Able to work well in a team environment; Good attention to detail, time management and organisational skills; Good communication and interpersonal skills; Structured and methodical approach to work with good analytical and problem-solving skills; High level of quality consciousness; Able to take ownership of assigned processes; Ability to work under pressure; Able to work independently with minimum supervision; Ability to evaluate data and draw conclusions independently; Able to design innovative solutions; Good note-taking ability; Able to generate enthusiasm and drive for commitment to excellence; Strong presentation skills and ability to deliver informative, well-organised presentations to team and management; Confident decision maker; Advanced conflict resolution skills; Strategic thinking; Cross-functional collaborationJak aplikować
Aplikuj online: https://www.jobs.pl/oferta/100098604/aplikuj
JOBS.pl · https://www.jobs.pl/project-manager-pharmacovigilance-oferta-100098604
















