Medical Manager Oncohematología

Medical Manager Oncohematología


Medical Manager Oncohematología

Detalles de la oferta

The CMM is a key strategic leadership role requiring therapeutic area expertise and clear business understanding to identify and address the relevant medical needs of clinical practice, to successfully support the optimal use of Roche products.

He/she links affiliate to Global Medical Affairs objectives to deliver on data generation, knowledge exchange / data communications, and to lead TAE engagement in a scientific manner.

The CMM acts as a guardian for high standards of compliance, ethics, and safety of Roche products, putting patients at the center of his/her actions

The Country Medical Manager (CMM)

Is a local role

Is a member of the affiliate MAs department

Works closely together with MKT team in a specific Therapeutic Area/Product

Responsible for

Development of the local Medical Plan

Medical expertise and customer insights to the Brand team

Design, oversight of execution, and report of clinical trials according to ICH-GCP, Roche SOPs and local regulations

Development of effective interactions with Clinical Operations (both PDG and PA/GPS), including but not limited to placing studies, provide input on feasibility, sites and investigators selection.

TAE engagement plan to support medical objectives: identification, development, and establishment of scientific relationship with TAEs

Support for PharmacoVigilance activities, including assurance of appropriate adverse event reporting in coordination with LSR

Support for Regulatory and Medical Information activities for selected products

Medical and regulatory clearance of promotional and informational materials

Development and management of the medical plan

Identify local data gaps, local studies protocol design, study planning (including budget), input to site selection and feasibility assessment, data dissemination strategy

Align the local medical plan with the local marketing, CT/IMT/DST strategy and global medical plan, under supervision of Medical Director

Congress overview and guidelines development

Medical expertise and customer insights to the brand team

Offer expert opinion aligned with LCT/IMT/DSC medical recommendations on scientific medical information to identify and develop effective peer-to-peer relationships to execute our product strategies, while holding high ethical standards, compliance to Roche SOP and local/international regulations

Research, collate, present and offer data insights related to the dedicated disease area and product(s)

Manage the integrity and accuracy of scientific and medical data communicated both internally and externally for promotional and non-promotional purposes.

Manage Medical Information activities in accordance with regional/local model, referencing global standard responses

Manage publication related activities according to Roche Policy and SOPs

Develop a customer centricity culture, making sure promotional/medical/scientific communications address HCP needs and optimize patient benefit and safety while keeping a fair balance and compliance with regulations and SOPs

Contribution to local clinical operations activities

Oversee the phase III-B/IV trial program by holding effective relationship with the Clinical Operations team

Provide early insights on new products and indications in close collaboration with the PDG group

Inform other Affiliate functions on Global planned studies

Design and implementation of patient support programs

TAE engagement plan and execution

Maintain regular contacts with investigators for key studies

Identify and develop scientific relationship with external TAEs/ experts who are qualified sources of insight and advice

Ensure that all activities towards external experts / TAEs are harmonized across the affiliate

Share Best Practices across customers to facilitate improved patients outcome

Planning and execution of relevant scientific advisory boards and expert meetings


Medical Degree with exceptional therapy area experience may be considered.


Professional experience within the pharmaceutical industry desirable but not mandatory

Knowledge of the overall drug development process relevant to pharmaceutical/biotechnology organizations

Experience in development and implementation of clinical trials

Experience in the principles and techniques of data analysis, interpretation, and clinical relevance

Experience of writing clinical publications and delivery of scientific presentations

Relationships with external TAEs, other thought leaders, and external organizations is strongly preferred


Knowledge of relevant therapeutic area

ICH, GCP and local regulations

Appreciates the diversity of working with multifunction teams

Knowledge of drug discovery & commercialization processes.

MS office literate

Fluent English language knowledge, written and verbal


Strategic thinking

Leadership skills

Analytical Skills

Results orientation

Communication, interpersonal and networking skills


Fuente: Bebee


  • Comercio – Mercadeo – Ventas / Supervisión de Equipos



  • Exchange

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