Company
healthcare
MedicalManagerHematology
“Medical Manager Hematology. Skills: Medical Affairs, Clinical study design, Clinical study execution, KOL engagement, Regulatory affairs, Medical materials review, Cross-functional input provision. Support the design, implementation and execution of Medical Affairs plans for assigned Therapy Area. Provide scientific information”
What You'll Achieve.
Achievement of annual targets for medical activities
Industry & Context.
Risk identification and assessment; Mitigation planning
What They're Looking For.
Must Have
Collaborating across boundaries, Operations Management and Execution, Project Management
Nice to Have
Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Internal Medicine, Job Description, Medical Information, Organization Skills, Patient Care, Stakeholder Engagement, Tcp/Ip Protocols, Utilization Management (Um)
What You'll Do.
implementation and execution of Medical Affairs plans for assigned Therapy Area
Provide scientific information
Help design & organise clinical studies
Build educational dialogue with KOLs and regulatory stakeholders
Ensure medical enquiries are responded to in a high quality
Provide medical/scientific input into the development and execution of clinical trial or clinical research related activities
Initiate and oversight of clinical studies / clinical research within the respective therapeutic area
Support country strategy for Non Interventional Studies/Investigator Initiated Trial activities
Coordinate review and approval of medical materials and locally developed promotional
Ensure medical materials provided from global or region for stakeholder engagement and events are tailored to local needs
and reviewed/approved per local/P3 guidelines
Ensure medical insights are provided to cross functional groups
Responsible for risk identification and assessment
mitigation planning as well as implementation and monitoring of appropriate internal controls within the area of responsibilities
Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt
Distribution of marketing samples (where applicable)
How You'll Work.
Team & Collaboration
Collaborating across boundaries; Provide medical insights to cross functional groups, including, but not restricted to: Pharmacovigilance, Regulatory affairs, Market Access, QA, Commercial teams, Brand team and others.
Communication Scope
Building educational dialogue with KOLs and regulatory stakeholders; Ensure medical enquiries are responded to in a high quality, timely manner; Ensure medical insights are provided to cross functional groups
Process & Methodology
Project Management, Support country strategy for Non Interventional Studies/Investigator Initiated Trial activities, Coordinate review and approval of medical materials and locally developed promotional, Ensure medical materials provided from global or region for stakeholder engagement and events are tailored to local needs, and reviewed/approved per local/P3 guidelines
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