Job Summary

The EMEA Director Therapeutic Interventional Oncology defines and implements the TIO Medical & Clinical strategy and tactics in the assigned EMEA territories and leads the medical and scientific intelligence related to TIO line. Main responsibilities include;

Lead the medical and scientific intelligence related to TIO line.

Further develop Terumo leadership within the oncology medical community.

Manage the EMEA TIO Medical Affairs team in the assigned territories.

Develop cross-functional interactions with EMEA and local business stakeholders (Marketing, Commercial, Regulatory, Market Access, Legal, Compliance…) to align Medical strategy and tactics that supports TIO portfolio within the assigned EMEA territories.

Lead the internal and external data dissemination across EMEA territories (medical information scientific communication, speaker briefing, internal training…).

Job Responsibilities

Upstream activities related to Radiation Oncology products Contributes to the Medical and Clinical strategy supporting the pre-launching/launching and post-market plan in good alignment and favorizing efficient collaboration with the Global Radiation Oncology strategy/team. Is responsible of collecting and sharing the medical insights (strategic medical advisory boards) and scientific intelligence (congress, publications, clinical trials pipeline, emerging technologies…) from the assigned EMEA territories to inform the business stakeholders and all relevant functions within the assigned EMEA region. Develops efficient synergies and collaboration with both Global Development Medical Program and Global Radiation Oncology teams.

Upstream activities outside the Radiation Oncology products (TACE, ablation products) within the assigned EMEA territories Is responsible to define & implement the Medical and Clinical strategy. Is accountable and responsible to collect and share medical insights (strategic medical advisory boards) and scientific intelligence (congress, publications, clinical trials pipeline, emerging technologies…) from the assigned EMEA territories to inform the business stakeholders and all relevant functions in the assigned EMEA region. Develops efficient synergies and collaboration with the Global Development Medical Program.

Dowstream activities related to the TIO portfolio within the assigned EMEA territories Is responsible to collect, review, manage the discussions with the Investigators and follow-up the Investigator-Initiated Studies program, from new proposal assessment to scientific communication (abstract, publication…). Contributes to the Company-Sponsored Studies program related to Radiation Oncology products, in an efficient collaboration with the Global Radiation Oncology team and other involved functions (EMCD, Regulatory…), and is responsible of designing the Clinical Development Plan outside the Radiation Oncology line (TACE, ablation products). Is responsible of disseminating the scientific data within the assigned EMEA territories throughout internal programs (business stakeholders training), (proactive and reactive) medical information and external scientific communications (advisory board, scientific/medical congresses, end-user meeting…). Is responsible of engaging meaningful and strategic partnerships with key opinion leaders, experts, medical societies and to increase Terumo leadership within the Oncology community.

People and team management Manages the EMEA TIO Medical Affairs team. Ensures the maintenance of the key competencies within the EMEA TIO Medical Affairs team by developing short/mid-term development/traing programs. Ensure that Associates are equipped and trained to cover their mission by developing annual Personal Development Plan. Ensures a high level of scientific knowledge and expertise in the Oncology and Interventional Oncology fields within the EMEA TIO Medical Affairs, at least in the key strategic indications. Contributes to Long-Range Plan and Budget preparation, in an efficient collaboration with the Global Senior Medical Director and Global Medical Development Program stakeholders.

Profile Description

MD/PhD or equivalent with at least 5-year experience in a managerial position

Experience within the field of Therapeutic Oncology is considered a plus

Able to effectively educate and influence stakeholders

Strategic mindset

Adaptability and flexibility - Innovative with the ability to coordinate and drive a complex and changing environment

Excellent Presentation and communication skills, ability to convince with influencing skills that can impact at a Regional and Global level

Patient & Customer & Market Insight - Highly patient and customer-centric and business-oriented mindset

Ability to work effectively in a matrix environment combing Global and EMEA considerations

Strong leadership skills, capable of driving a multi-cultural, remote team

Must be able to travel internationally on a frequent and business-needed basis; anticipate approximately 25% to 50% travel

Offer

We offer you an exciting fulltime position in an international medical devices company and a pioneering role within the further development of the Therapeutic Interventional Oncology field. You can count on a competitive compensation package in line with your experience. In addition, Terumo embraces the evolved reality of ways of working, offering the possibility to opt for a hybrid way of working.

EMEA Medical Affairs Director Therapeutic Interventional Oncology

Others also viewed

gespecialiseerd technieker EMA

Testing and certification engineer

Certificatie ingenieur – Wegenbouwproducten

EMEA Medical Affairs Director Therapeutic Interventional Oncology