Senior Director, Global Collaborative Research, Hematology Position Available In New York, New York

ResponsibilitiesThe Senior Director, Global Collaborative Research, Haematology is accountable for the management and oversight of Menarini Stemline’s haematology collaborative research portfolio, encompassing independent (e.g. ISR, IIT, ISS, IIS, etc.) and collaborative interventional and non-interventional studies. This is a highly collaborative role, providing study, project, and program support to internal stakeholders, cross-functional departments, and external sponsor teams. This individual will be responsible for the lifecycle (e.g. start-up through close out) of their portfolio of studies, ensuring that Menarini Stemline adheres to all applicable SOPs, laws, regulations, and best practices in the execution of our research program.

Key Responsibilities:

Independently manages and provides oversight for all components of Menarini Stemline’s global hematology collaborative research portfolio, encompassing independent and collaborative scientific research initiativesParticipates in the Medical Affairs Research Committee (MARC) and related governance meetings, ensuring that decisions rendered are carried out within the new and existing portfolioDrives study start-up activity for Menarini Stemline, including protocol review, contracting, financial set-up, document collection, drug supply set-up, and ultimately study activationMonitors and tracks activities and key milestones on individual studies throughout their lifecycle, summarizing this information for any relevant reporting, cross-functional communication, and stakeholder awarenessMonitors and manages individual study budgets for assigned portfolioCollaborates with Information Technology, Quality Assurance, Compliance, and other departments to optimize systems, processes, policies, and standard operating proceduresDevelops and maintains relationships with external collaborators, including healthcare professionals, healthcare organizations, research organizations, site staff, and other supporting rolesSupports the growth and evolution of Menarini Stemline through the development of novel or best practice solutions to problems of large or small scaleEscalates issues proactively, recommending and implementing innovative processes to address and improve identified difficultiesSupports the development of action plans that address compliance, safety, and administrative issues, both internally and externallyQualificationsBachelor’s degree or equivalent, preferably in life sciences or healthcare fieldMinimum of 5 years of relevant experience in an academic clinical research setting and/or pharmaceutical/biotech industry, preferably in medical affairs research operations or clinical operationsExperience managing independent or collaborative research in Haematology/Oncology or a related fieldGlobal (e.g. US, EU, LATAM, APAC, etc.) experience in the planning, launching, maintenance and closure of interventional and non-interventional studies, including relevant knowledge of

CFR, ICH

GCP, contracting standards, and GDPR/data privacy requirementsSelf-starter comfortable working in a virtual environment with cross-functional teams in a variety of geographiesScientific agility with ability to summarize complex scientific or medical terms to a broad audienceResourceful with keen critical thinking skills; ability to utilize available resources to drive solutionsAbility to prioritize urgent and important tasks and take necessary actions to inform or escalate to management and stakeholders as necessaryAbility to influence and work effectively across functions and operate in a complicated and evolving matrix environmentMust possess excellent oral and written English communication skills, including presentation skillsBasic technical and electronic skills, such as databases, systems, and Microsoft Office computer programsMenarini Stemline is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

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