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Medical Director Benelux (Tilburg, NL)

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Medical Director Benelux-00000LYC

Omschrijving

Janssen Benelux; is an international pharmaceutical company with a formidable track record in the field of scientific research & innovation. It consists of 2 subsidiaries of the global health care group of Johnson & Johnson: Janssen-Cilag B.V. in the Netherlands and Janssen-Cilag NV in Belgium and Luxembourg. Benefiting from the successful launch of many pioneering pharmaceutical products and building on a highly promising research pipeline Janssen is firmly committed to setting new clinical standards well into the future. Moreover, we are passionate about adding value to the broader health care environment by developing sustainable, integrated health care solutions in close cooperation with patients, physicians and other stakeholders, based on partnerships of trust and transparency.

She/He leads the Medical Department in the Benelux. The Medical Director is responsible for the Medical leadership in the 3 countries in which building and nurturing a network of relevant key opinion leaders and other scientific and clinical stakeholders is crucial. The medical strategy, the design, development and implementation of Medical programs fall under his/her responsibility. The Medical Director is also responsible for the full adherence to all local and relevant international regulations concerning regulatory, Pharmacovigilance and QA (Quality Assurance) matters as well as for advertising and promotion rules. The Medical Director is a member of the Janssen Benelux Management Board and in that function also jointly responsible for setting out the long term, overall company strategy.

Tasks & responsibilities:
- Foster a culture of Medical Excellence at a scientific level and of internal and external customer orientation, aligned with the J&J Leadership Imperatives (Connect, Shape, Lead, Deliver).
- Be responsible for all compliance obligations of Janssen Benelux (QA, Regulatory and Pharmacovigilance) including quality review and approval of educational and promotional materials for use by internal stakeholders.
- Implement the company’s drug surveillance/product safety program which includes, but is not limited to the follow up on adverse reaction reports.
- Represent Janssen Benelux in the external medical and scientific communities. Personally connect with the Key Medical Opinion Leaders and medical and scientific associations in the Benelux and develop solid relationships based on trust and common clinical objectives.
- Collaborate and connect with the Benelux Global Clinical Operations (GCO) organization regarding Phase I – Phase III clinical trials.
- Ensure that the medical, compliance and quality objectives are aligned with the goals & mission of Janssen Benelux and the broader Corporate goals & objectives.
- As a member of the board, have joined responsibility for the Janssen Benelux Strategy and execution.
- Ensure optimal alignment between the medical activities and the priorities of the cross-functional Therapeutic Area Teams (CVT’s) and other internal teams and stakeholders.
- Maximize the added value of the medical department and expertise towards the overall company objectives, by stimulating the Medical team to active (cross-functional) cooperation with internal stakeholders. Lead by example through collaboration with other MB members.
- Demonstrate leadership in representing the Benelux in the Janssen European organization (EMEA) medical community. Benchmark the Benelux medical strategies, goals and activities with EMEA.
- Lead and manage the medical department, including project and people responsibilities.
- Lead and drive continuous improvements to create an environment that encourages and recognizes creativity, innovation, teamwork, risk taking and empowerment.
- Recruit top talents and be passionate about their development. Ensure diversity within the team and be inclusive towards other opinions and backgrounds. Drive a credo-based culture and behavior.

The Medical Director is a member of the Management Board and reports to the Managing Director Benelux. Direct reports to this position are the Medical Affairs Director, the Head of Medical Science Liaisons and COE Medical Education and the Head of COE Quality & Compliance (containing QA, Regulatory and Pharmacovigilance).The position has a clear Benelux scope, but will be based in Tilburg, The Netherlands.

Kwalificaties

Qualifications:
- Scientific Degree: Medical Doctor
- 12+ years working experience
- 3-4+ years industry/business experience in a relevant area for this function (e.g.Medical Affairs or Clinical R&D).
- 6+ years team leadership or functional line management experience
- Excellent analytical, communication, decision-making and leadership skills
- Highly committed to people development
- Team player
- Easy connector & stimulator for others to optimally liaise with internal and external customers and partners
- Demonstrating leadership in compliance and quality
- Languages: Dutch, English: spoken, written
- Working experience abroad is favorable

BE VITAL in your career, Be seen for the talent you bring to your work. Explore opportunities within the Johnson & Johnson Family of Companies.

Primaire locatie: Europa/Midden-Oosten/Afrika-Nederland-Noord Brabant-Tilburg

Organisatie: Janssen-Cilag Netherlands (8345)

Functie: Medische zaken

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