• Empresas
  • Sueldos
  • Entrevistas
  • Empleos

Empleo de Medical Manager Immuno-Oncology (Genitourinary)
Roche en Buenos Aires - CF

Descripción del puesto de trabajo

Medical Manager Immuno-Oncology (Genitourinary)

Medical Manager Immuno-Oncology (Genitourinary)

Argentina, Buenos Aires

Apply now! Print
* Job facts

The MM 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 MM 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 Medical Manager (MM)

  • Is a local role
  • Is a member of the affiliate MAs department
  • Works closely together with MKT team in a specific Therapeutic Area/Product

Reports to:

  • Senior Medical Manager or Affiliate Medical Director
  • Direct Reports: MSLs where applicable

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
  • A part-time field-based resource for TAEs and investigators delivering the scientific information that they require in the context of their work, in accordance to local laws, regulations and codes, and Roche/Genentech's SOPs
  • 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

Others (depending on the size & structure of the Affiliate)

  • Actively contribute to the IMT (Key countries)
  • Oversight of the execution of clinical trials (countries with no separate Clin Ops organization in-house)
  • Inform Local Safety Responsible person of safety issues according to Roche safety requirements; scientific support and follow-up on product safety issues
  • Support regulatory activities, including preparation of relevant data for new products/indications’ application and label updates
  • Provide medical/scientific support and training for internal staff or vendors
  • Support and collaborative work with pharmaco-economic and access teams, providing relevant efficacy and safety data on dedicated products including the design and implementation of HEOR studies
  • Act as medical expert for requests from external organizations, e.g.. media (via PR department)
  • Design and implementation of congresses booth and non promotional symposia and selection of recipients of travel sponsorship
  • Evaluation of incoming requests of research & educational grants
  • Who you are

You’re someone who wants to influence your own development. You’re looking for a company where you have the opportunity to pursue your interests across functions and geographies. Where a job title is not considered the final definition of who you are, but the starting point.
* Medical Degree
* Experience
* Professional experience within the pharmaceutical industry / therapeutic area 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
* Who we are

At Roche, 94,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.

Roche is an equal opportunity employer.
* Job facts
* Location Argentina, Buenos Aires
* Function Medical Affairs
* Subfunction ****
* Schedule Full-time
* Job level Manager
* Job type Regular Employee
* Division Roche Pharmaceuticals
* Posted since 2018/02/16
* Posted until 2018/03/18
* Job-ID 00454021

  • Get in touch

RRHH
* You could also like these jobs

Pharmacovigilance Country Cluster Lead – LATAM

Argentina

Medical Science Liaison (Oncology Gastrointestinal)

Argentina, Buenos Aires

Medical Manager Immuno-Oncology (Genitourinary)

Argentina, Buenos Aires

Apply now!

Descubrí más