This is a remote position.
Overview:
From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp
Our Fortune 500 Pharmaceutical Client has an exciting opportunity for a Pharmaceutical Project Manager.
Job Summary:
The Pharmaceutical Project Management (PPM) provides strategic and operational leadership and support to projects designed to increase patient enrollment in Oncology Clinical Trials. This requires working cross-functionally to translate strategy into execution to deliver medicines to patients.
Responsibilities and Job Requirements:
Responsible for Providing support in scheduling meetings, developing timelines, identify and consider interdependencies, minutes/agendas, and tracking deliverables and budget (65%).
- Responsible for managing scope and translating strategies and objectives into executional tactics across multiple workstreams
- Work with teams to create and execute project plans and drive communication of key decisions/results to stakeholders
- Identify interdependencies and cross functional
- Drive development and tracking of project budgets
- Proficient in self-management and organizational skills; able to manage workload on diverse set of projects, set personal and team priorities while adjusting as needed
- Project Management Tools/IT Management:
- Provide quality and timely content using project management tools
- Monitor and prioritize team risks to suggest ways to avoid/mitigate risks and initiate contingency plans as needed
Team Productivity, Engagement, and Facilitation (30%)
- Strong interpersonal and teambuilding skills; able to develop effective teamwork between team members with diverse styles and roles
- Deliver effective coaching and feedback to individuals and/or team; help teams resolve conflict together
- Lead teams to make data and judgment-based decisions
Application/Improvement of Processes (Shared Learning) (5%):
- Leads through shared learning, process improvement, and identification of special/complex needs
- Share learnings and retrospectively review lessons learned Bring forward areas for continual process improvement to decrease drug development cycle times and cost
- Bring forward areas for continual process improvement to decrease drug development cycle times and cost
Educational Requirements:
- Four-year degree preferably in a health-related, scientific, or engineering field with a minimum of 3 years of work experience in the pharmaceutical industry, drug development, clinical trials, or project management and/or product development.
Additional Preferences:
- Higher degrees or certifications (e.g., MS., MBA, Master’s degree in Project Management or PMP)
- Demonstrated direct leadership in cross-functional environment
- Knowledge of or previous experience with Clinical Trials or Oncology (or both) and application of project management tools and processes in cross-functional settings
- Proficiency with Microsoft Word, Excel, PowerPoint, Project (or related tools) and capable of maintaining appropriate project documentation
Other Details:
- Part-time: 20 Hours/Week
- Contract Length: 18 months
- Remote but need to travel to Indianapolis annually
EEO Employer:
Pharmavise Consulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Pharmavise Consulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require accommodation in using our website for a search or application, please contact info@pharmavise.com.
Pharmavise Consulting Corp. is a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients. When you join Pharmavise, you become part of a team that values Excellence Through Quality.