Hobson Prior currently have an exciting opportunity for a Senior Project Manager to join a Swiss global healthcare organisation who are focused on offering medical solutions in order to transform patients' lives. As the Project Manager you will be dedicated to supporting Technical Regulatory Teams in managing programs efficiently and effectively and in executing regulatory activities.

Job Responsibilities:

• Support TRTs and TRLs in developing TRT charters, plans, detailed schedules, deliverables list, status updates, resource requests and program specific communications for individual programs in the regulatory product portfolio including large molecules, small molecules, devices, antibody drug conjugates.
• Be a thought partner to TRLs and team members, facilitate and drive team discussions based on high-level program knowledge.
• Provide project management support to TRTs at any stage of the drug development lifecycle (i.e. early or late stage development, marketing authorization or post-launch marketed phases).
• Provide support of PTR Strategic Focus Areas and cross-organizational initiatives.
• Coordinate and facilitate TRT meetings and all aspects of program information management ensuring robust documentation and communications.
• Partner with TRLs and teams, facilitating team interactions and mobilizing teams to deliver successfully on the agreed objectives.
• Perform project management activities to support products for global market applications and product life-cycle activities.
• Support issue-specific multi-product impacting regulatory projects to ensure alignment of regulatory strategy and compliance across the Biologics and Small Molecule platforms.
• Ensure regular and meaningful project communications, including dashboards, reports and metrics, to enable timely information and analyses to key stakeholders and decision makers.
• Ensure product information flows between TRT members to ensure transparency, informed decision making, and optimal alignment of all technical regulatory deliverables.
• Maintain linkage between TRT and TDT or TPT ensuring alignment of assumptions and communications at all times.
• Facilitate regulatory program risk assessment and align with TPM and TDT processes. Develop, execute and report on risk mitigation or issue resolution activities.

Key Skills:

• Excellent interpersonal skill (communications, organizational skills and leadership mindset).

Requirements:

• A minimum of 8-10 years' experience in project management in pharma.
• Excellent regulatory knowledge and experience.
• Excellent understanding of drug development and CMC.
• BA/BS or MS in Scientific, Technical, Engineering or Business discipline. Advanced degree preferred.
• Prior experience with programs and portfolios in a strategic context is a plus.
• Knowledge of agile methodology is highly desired.

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.