Associate Director Clinical Trial Lead (Boston area) at Millipore Corporation in BILLERICA, Massachusetts

Job Description:

Manages multiple studies, projects, and work streams with high complexity, risk, impact and reach, typically Ph III and registrational/pivotal studies in mixed sourcing models.Demonstrates skills in successfully leading large-sized global project teams in a matrix organization and directs, influences and motivates people; coordinates stakeholders from closely related areas and beyond, creating a positive working climate.Leads the development of the clinical trial strategy while accountable for successful project execution and delivery of clinical operational plan within the budget, timelines and quality standards agreed upon by Governance Committees.As a core member of the Clinical Operations Team and leader of the Clinical Trial Team, aligns clinical trial team with organizational goals and objectives of the Clinical Operations Team and/or Global Program Team.Filters, prioritizes, analyzes and validates complex and dynamic information from a diverse range of external and internal sources to respond to technical operational and organizational challenges in a holistic manner to mitigate risks.Exhibits Subject Matter Expert level understanding of multiple functions and functional processes. Familiar with and considers overall business objectives and company strategy.Acts as a senior advisor and mentor within the team and beyond and serves as best practice resource within own discipline or as technical expert on cross functional teams or projects.Ensure all study management activities will be completed in accordance with SOPs/WI, local regulatory guidance including ICH-GCP; audit & inspection leadership- interviewee & responses.Contribute to non-study -related initiatives in addition to study assignments. Provide reports to senior management, including updates on financials, forecasts and timelines independently. Demonstrates creativity and innovation to support projects from a strategic perspective, able to predict the result of action in advance and evaluate options to achieve goals.



Who you are:




Minimum Qualifications:



At least 10 or more years in clinical research in a CRO or Pharmaceutical/Biotechnology Industry environment7 years of in-depth knowledge and experience in clinical trial managementAdvanced degree desirable (MPH, MS, MA, MBA, PharmD); PM certification (CPM, PMP) desirableProven experience in all aspects of clinical study planning and startup (including budget and resource planning) and in executing the complete range of clinical study activities, from startup through final study report.



Preferred Qualifications:



Experience in multiple Therapeutic Areas (oncology and immunology preferred)Requires substantial to extensive professional experience in relevant disciplines and substantial project management experience. Requires expert knowledge and experience in own discipline and beyond which may also require good market and competitor knowledgeStrong leadership competencies and influencing skillsProven team dynamic knowledge and skills and ability to foster partnerships across projects and multidisciplinary teamsGrowing expertise in drug development, including some knowledge of interfaces and interdependencies of clinical development with other functions (e.g., nonclinical & pharmaceutical development, regulatory, commercial/marketing)