Oncology Msl Solid Tumors North Italy

2 settimane fa

Roma, Italia Takeda Pharmaceutical A tempo pieno

Are you looking for a patient-focused, innovation-driven company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as an **Oncology MSL** in **North Italy** working on Solid Tumors, with focus on **Colorectal and Lung Cancer** diseases. You’ll be part of a field-based team providing medical expertise and contributing to the achievement of the strategic goals.

**Role objectives**

Identify and develop strong sustainable peer to peer relationships with external stakeholders to support the medical/scientific credibility of the company
- Continuously screen, review and analyze scientific literature; generate summaries & critical assessments if appropriate
- Use specific disease and product knowledge to develop Takeda in a given therapy area; i.e. answer medical/technical unsolicited enquiries from HCPs, provide accurate and non-promotional scientific information relating to licensed and unlicensed indications following unsolicited requests from HCPs, etc.
- Proactively identify and develop long term peer-to-peer relationships with opinion leaders and other relevant stakeholders in order to understand their needs, segment them accordingly and implement targeted approach and tactics in order to present medical data in the most efficient way
- Act as field-based reference points of scientific and clinical expertise for sales force and other internal stakeholders (e.g. Market access) through training and ad-hoc support, in alignment with Takeda project teams
- Supports ongoing and future Company Sponsored Studies i.e. provides LOC review of proposed CRO site lists, attendance at Global/Regional Investigator Meetings, attends motivational site visits, provides site/investigator feedback to clinical operations etc. following the appropriate request from Global Development Operations and informs other LOC functions on progress in site involvement process in a timely manner
- Capture and share in-field insights to support medical and scientific strategy and business development. Shares in-field insights in a compliant manner with relevant business functions.
- Participate in the development and implementation of key medical activities (e.g. Advisory boards, medical education and peer-to-peer training activities)
- Provides clinical presentations and medical information as necessary
- Facilitates unsolicited requests from HCPs for investigator-initiated sponsored research proposals through engagement with Global External Research on IISR proposals and on Medical Affairs Company Studies (MACS)
- Development and support of national disease registries and RWE projects for relevant disease areas
- Understands leverage points of the patient journey
- Act according to Corporate, Compliance, Ethical codes and Legal standards
- Promotes, encourage and demonstrate commitment to Takeda-ism philosophy and values.
- Communicate to pharmacovigilance department any adverse reaction at the time of becoming aware of it, following company’s internal procedures.
- Ensure development and implementation of an annual quality plan within the scope of responsibility

**Requirements**:

- Scientific PhD or Master’s Degree, a medical qualification is a plus
- At least 1 year of experience as MSL/equivalent medical affairs (Desirable), or in Contract Research Organization (CRO) position is a plus.
- Experience as MSL in oncological areas in particular Colorectal and Lung Cancer diseases (Desirable).
- The knowledge of digital technologies of Omnichannel engagement (OCE).
- Working in a matrix management environment.
- Clinical trials experience and good understanding of clinical trial data and study design (Desirable).
- Experience of working with scientific and clinical experts at all levels in both 1 to 1 and group settings (Desirable).
- Experience in providing clinical data and Oncology area training to both medical and non-medical colleagues (Desirable).

**Skills**
- Fluent written and spoken English, minimum level required B1
- Computer literacy and willingness to discover new technologies
- Good communication skills, both spoken and written.
- Ability to work at a high scientific and clinical level to ensure quality peer-to-peer engagement with external stakeholders
- Clear and concise presentation of clinical data, including discussion of statistical and clinical relevance in line with key messages
- Autonomous, in-field work whilst contributing to central Medical Affairs
- Proven track record of teamwork, leadership, timely decision making and results orientation in meeting objectives
- Project management skills to manage milestones and deliver tasks within timeframe
- Desire to put people first and demonstrate the values of Takeda-ism

**Locations**:Lombardia, Veneto or Emilia Romagna. Italy

**Locations**:
Rome, Italy

**Worker Type**:
Employee

**Worker Sub-Type**:
Regular

**Time Type**:
Full time

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