Vacancy expired!
USD200,000-USD275,000Set milestones, budget forecasting, resource planning, scenario planning
Develop a program plan based off program needs
Support the management of cross-functional teams, including research, clinical, nonclinical, regulatory, and CMC, development
Provide strategic guidance and drive situational planning
Deliver high-quality project management services to drive program success
Ensure effective and timely communication to team members and senior management regarding deliverables, key milestones, achievement of external/internal commitments, timelines, budgets, and key events.
Implement cross functional program risk management plans including, risk and opportunity identification and assessment, mitigation strategies and contingency planning
Manage team meeting operations such as planning agendas, scheduling meetings, and proactively following-up with team members to meet deadlines
MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants.BS in a relevant scientific discipline (higher level degree preferred)
10+ years of biotech/pharma experience
8+ years of experience managing cross-functional teams (small molecule development and oncology experience is preferred)
Thorough understanding of drug development from pre-clinical to clinical stages
Leadership skills to be effective in a matrixed organization with geographically dispersed teams
Proven track record of planning and managing complex programs across all phases and executing cross-functional deliverables across Research, Clinical Development, CMC, Commercial, and Market Access
Leadership/Management experience required
Exceptional listening, speaking, and writing skills
High level of attention to detail
Our client is a biotechnology company treating genetically driven diseases by using validated biology and optimizing its effectiveness. They execute everything from Research and Development all the way to commercialization. Their lead therapeutics are treating patients with rare disorders, and drastically improving their lives. Currently in Phase II/III with their leading assets, this company is targeting a BLA submission in 2023.Competitive salary
Performance-based bonus
Ability to work fully remote
Company stock package
Insurance coverage (health, dental, life, and disability)
Unlimited time-off
401(k) plan
Commuter/parking benefits if working hybrid model
Vacancy expired!