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ProPharma Group

Regulatory sciences consultant for life sciences

Director Product Lifecycle Management

Program ManagementPosted on Nov 9
Full-timeUnited StatesNo salary listed

About the Job

Requirements

  • Demonstrated knowledge of the overall drug development process relevant to pharmaceutical and biotechnology operations.
  • Demonstrated knowledge of Good Manufacturing Practices and ISO relevant to Product Lifecycle Management.
  • Working knowledge and understanding of best-practice alliance and collaboration management principles, concepts, techniques, and tools in support of client business expansion.
  • Understanding of criteria for selection in the pharmaceutical and biotechnology industries in support of partnership development and recruitment of needed talent.
  • Advanced proficiency with PowerPoint, Word, Excel, Visio, Project, OneDrive, and SharePoint.
  • Strong proficiency with project management practices, tools, and methodology.
  • Proven experience using project management software to manage complex project timelines and resources, such as Microsoft Project or other project management enterprise software.
  • Ability to identify and develop new clients.
  • Experience supporting sales activities for project services to clients.
  • Supervisory experience, including employee hiring and retention, oversight, performance review, employee development, and discipline.
  • Ability to assess and resolve difficult business situations and communicate complex issues simply.
  • Ability to organize and manage multiple projects.
  • Ability to make effective and persuasive presentations.
  • Ability to develop relationships with customers and key stakeholders and manage conflict.
  • Ability to earn and maintain a client's confidence through appropriate planning, organizing, controlling, and directing of a project.
  • Proven track record of sound decision-making and judgment.
  • Ability to think ahead, take initiative, maintain confidentiality, prepare action plans, meet deadlines, and work in a team environment.
  • Excellent written and oral English communication skills.
  • High attention to detail.
  • Bachelor of Science or Bachelor of Arts degree in the life sciences, unless substituted with 15 years of relevant work experience.
  • At least 15 years of multidisciplinary experience in the pharmaceutical and biotechnology industries.
  • At least 15 years of direct project management experience in small-molecule, large-molecule, or device development.

Responsibilities

  • Deliver all assigned work successfully.
  • Facilitate project team meetings, cross-functional communication, and decision-making to ensure alignment with internal and external stakeholders.
  • Oversee and manage project financials, prepare project team budgets covering resources and costs in collaboration with Finance and other cross-functional departments, and evaluate budget compliance and project billings on an ongoing basis.
  • Plan, assign, and direct work when representing project leadership.
  • Audit Product Lifecycle Management projects for correct approach, consistency, and quality.
  • Support project sales with Business Development by developing and reviewing content and participating in sales meetings.
  • Support staffing of client projects by identifying and recommending resources, conducting résumé reviews, and interviewing resources as requested.
  • Support development of annual Product Lifecycle Management marketing and sales plans and materials, including thought capital and webinars.
  • Participate in and present at industry associations and information exchanges related to developing guidance and practice.
  • Understand and track Product Lifecycle Management industry trends, determine how to leverage them for clients, and develop potential service offerings.
  • Provide responsible employees with written functional descriptions of their responsibilities, duties, and authority.
  • Ensure personnel complete performance management processes, including goal setting and performance evaluations, in a timely manner.
  • Carry out supervisory responsibilities in accordance with organizational policies and applicable guidelines.
  • Manage staff utilization.
  • Participate in internal or client-required staff training.
  • Enforce human resources policies and procedures with support from human resources staff.
  • Attend management team meetings as required.
  • Perform other duties as assigned.

Desired Qualifications

  • An advanced degree in a scientific discipline.
  • PMP certification or an appropriate comparable certification such as PRINCE2.
  • Fluency in an additional language.

About the Company

ProPharma Group

Regulatory sciences consultant for life sciences

ProPharma Group provides regulatory sciences consulting and related services for drugs, biologics, medical devices, and diagnostics on a global scale. Its offerings cover the full lifecycle, from early development and clinical trials to regulatory approval and post-market activities. The company’s services include regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology, delivered by a team of over 2,500 professionals with more than 20 years of operation. ProPharma Group differentiates itself by providing expert, end-to-end regulatory and life sciences solutions across multiple product types and stages, helping pharmaceutical, biotechnology, and medical device companies navigate complex regulatory and compliance challenges. The goal is to help clients bring safe and compliant products to market efficiently while maintaining ongoing lifecycle support.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Raleigh, NC
Founded
2001

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