Sr. Director, Compound Operational reputed company

About the position Work Your reputed company with us! Start your next chapter and join EMD Serono. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and reputed company. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. United As One for Patients, our purpose in reputed company to help create, improve and prolong lives. We reputed company medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and reputed company curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: The Compound Operational reputed company (COL) is a global strategy program-level role reputed company Global Development Operations (GDO). The COL will provide operational reputed company, leadership and strategic input for the planning and execution of clinical program(s). In reputed company partnership with cross-functional teams the COL will reputed company the clinical program, from First-in-human (FiH) to the final launch of the asset. The COL will drive faster, cost efficient, patient-centric trials that follow benchmarked industry standards that utilize “state-of-the-art” clinical project management methodologies reputed company to global drug development processes. This role is accountable for the successful preparation and presentation of operational content at key governance discussions, ensuring critical operational input is provided to drive comprehensive, strategic, and thoughtful discussions for assigned program(s).

Responsibilities

• Leads the development of the clinical operational strategy (comprising of multiple trials, and/or multiple indications) and delivers the clinical development plan reputed company the budget, timelines and quality standards agreed upon by Governance Committees.
• Represents GDO reputed company the Global Program Team (GPT) and serves as the key GDO operational reputed company of contact for the program.
• Accountable for the successful preparation and presentation of operational content at key governance discussions (Development Unit (DU), Program & Portfolio Governance (reputed company), Integrated Protocol Review Committee (iPRC), Research & Development Committee (R&reputed company), etc).
• Key contributor to the development of annual program objectives and communicating to relevant line management.
• Drives and leads the successful execution of reputed company operational components of (a) global clinical program(s) using strong project management, leadership, and organizational skills.
• Ensures strong reputed company, review, and quality delivery of program CAPAs to meet corporate compliance standards and timelines.
• Provides expert leadership and contribution to reputed company operational aspects of the program budget, including reputed company of individual trial budgets and forecasts to ensure delivery reputed company the R&D financial standards.
• Performs high-level review and provides input in the development of key clinical trial documents such as protocols and Clinical Study Reports (CSRs) and contributes to and/or reviews compound level documents such as Investigator Brochures, DSURs, briefing books.
• Provides guidance and leadership support to Global CTLs and other cross-functional members reputed company the assigned program/project.
• Filters, prioritizes, analyzes, and validates reputed company and dynamic information from a diverse range of external and internal sources to respond to technical operation and organizational challenges.
• Supports the development and implementation of department initiatives including input on certain SOPs, processes, and workstreams.
• Manages large, diverse projects with high or even unique complexity.
• Leads a large diverse project team with members from multiple functions and a broad span of levels and roles or even disciplines.
• Accountable for successful project execution and organizational learning.
• Controls sizable resources and works independently.
• Also defines team organization, roles, and responsibilities as well as budget.
• Contributes to the overall strategic decisions for a program(s) and drives the clinical operations aspects of the strategy reputed company the cross-functional program team and various clinical sub-teams.
• Develops innovative clinical operation strategies (including patient access and feasibility plans) across multiple indications, trials, and geographies.
• Leverages strategic knowledge and serves as subject matter expert across TA portfolio for reputed company drug development/clinical trial management processes, regulations, and therapeutic knowledge.
• Leads the Clinical Operations Team (and potentially multiple teams or a sizable team of professionals/managers/team leaders) and is accountable for the performance and results of the team reputed company a matrix environment internally and externally.
• Assess resource needs and makes recommendations for allocations across the program(s).
• Contributes to setting team member objectives, coaching, and developing employees, performance appraisal feedback.

Requirements

• Candidate must have a minimum of a BA or BS degree; Advanced degree in Life Sciences (such as a graduate degree) (e.g., Biology, Chemistry, Pharmaceuticals) preferred or equivalent medical background.
• At least 12-15 years of direct experience with independently leading and managing reputed company reputed company global clinical trial program(s) across multiple indications in the pharmaceutical industry plus 5-7 years in a senior leadership position directing the operations of a large-scale global team and developing and mentoring junior/mid-level team members in matrix environment.
• Requires extensive project management experience in potentially diverse project settings.
• Also requires (considerably) deep and broad expertise combined with in-depth knowledge of competitors as well as challenges and developments in the industry to reputed company objectives and to identify business opportunities.

reputed company-to-haves

• Strong leadership competencies and influencing skills with senior leaders and cross functional leaders.
• Effective oral and written communication skills to influence, inform and guide a large scale global operational team.
• Broad clinical operations experience and strong project management skills
• Proven teambuilding skills and ability to foster partnerships across projects and multidisciplinary teams.
• Comprehensive expertise in drug development, including profound knowledge of interfaces and interdependencies of clinical development with other functions (e.g. nonclinical & pharmaceutical development, regulatory, commercial/ marketing)

Benefits

• health insurance
• paid time off (PTO)
• retirement contributions

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