Senior Project Manager - Therapeutics
Telix Pharmaceuticals Limited
5 hours ago
Remote friendly (United States)
United States
Operations
Senior Project Manager
Key Accountabilities
- Manage all aspects of the product development plan, including activity planning, budgets, schedule adherence, resourcing, and milestone reporting.
- Engage with senior leadership to define project strategies and objectives; lead complex, multi-faceted projects across functional areas.
- Support alignment of project goals with company strategic objectives.
- Maintain internal project management software (SmartSheet) to ensure accurate scheduling, risk assessment, and team data integrity.
- Develop, maintain, and report project schedule information and baselines using standardized dashboard reporting.
- Facilitate regular project update meetings with project teams.
- Quantify cost and schedule changes for submission to change management.
- Contribute to integrated project teams in a matrixed organization.
- Develop and manage cross-functional reporting relationships to ensure traceability to other systems.
- Proactively identify and mitigate risks to ensure smooth project progression.
- Maintain ongoing communication with stakeholders to ensure alignment and visibility on progress and challenges.
- Act as key internal contact for supervised projects.
- Work with department leadership to ensure all reporting is met.
- Independently manage complex, late-stage, high-priority programs.
- Coach, review, and delegate work for team members and/or other PMO staff.
Education
- Bachelor’s degree in science or life sciences discipline, or equivalent life science experience.
- PMP certification strongly preferred.
Experience
- 6+ years in pharmaceutical/drug development/biotechnology, including Ph1–Ph3 readiness and execution.
- 5+ years of project management experience leading multiple concurrent projects across functions and development stages.
- 5+ years in financial management (budgeting, tracking, forecasting, resource allocation).
- Proficient in at least two drug development functions (e.g., clinical operations, manufacturing development, regulatory affairs, or non-clinical development).
Skills and Competencies
- Proven ability in cross-functional teams; able to support and influence strategic direction of drug development initiatives.
- Advanced knowledge of project scheduling tools; SmartSheet experience preferred.
- Ability to ensure project execution aligns with overarching business strategies.
Benefits
- Competitive salaries, annual performance-based bonuses, equity-based incentive program, generous vacation, paid wellness days, and support for learning and development.
Key Accountabilities
- Manage all aspects of the product development plan, including activity planning, budgets, schedule adherence, resourcing, and milestone reporting.
- Engage with senior leadership to define project strategies and objectives; lead complex, multi-faceted projects across functional areas.
- Support alignment of project goals with company strategic objectives.
- Maintain internal project management software (SmartSheet) to ensure accurate scheduling, risk assessment, and team data integrity.
- Develop, maintain, and report project schedule information and baselines using standardized dashboard reporting.
- Facilitate regular project update meetings with project teams.
- Quantify cost and schedule changes for submission to change management.
- Contribute to integrated project teams in a matrixed organization.
- Develop and manage cross-functional reporting relationships to ensure traceability to other systems.
- Proactively identify and mitigate risks to ensure smooth project progression.
- Maintain ongoing communication with stakeholders to ensure alignment and visibility on progress and challenges.
- Act as key internal contact for supervised projects.
- Work with department leadership to ensure all reporting is met.
- Independently manage complex, late-stage, high-priority programs.
- Coach, review, and delegate work for team members and/or other PMO staff.
Education
- Bachelor’s degree in science or life sciences discipline, or equivalent life science experience.
- PMP certification strongly preferred.
Experience
- 6+ years in pharmaceutical/drug development/biotechnology, including Ph1–Ph3 readiness and execution.
- 5+ years of project management experience leading multiple concurrent projects across functions and development stages.
- 5+ years in financial management (budgeting, tracking, forecasting, resource allocation).
- Proficient in at least two drug development functions (e.g., clinical operations, manufacturing development, regulatory affairs, or non-clinical development).
Skills and Competencies
- Proven ability in cross-functional teams; able to support and influence strategic direction of drug development initiatives.
- Advanced knowledge of project scheduling tools; SmartSheet experience preferred.
- Ability to ensure project execution aligns with overarching business strategies.
Benefits
- Competitive salaries, annual performance-based bonuses, equity-based incentive program, generous vacation, paid wellness days, and support for learning and development.