Medical Advisor Oncology Benelux a.i.

Implement the country medical affairs plan and other key medical affairs initiatives in collaboration with internal and external stakeholders in alignment with the medical strategy Nothern Europe Oncology division with the highest ethical and compliance standards

Client Details

An innovative global healthcare company with products treats rare diseases.

Description

• Conduct internal and external medical education to enhance disease and product knowledge and awareness

• Regular external scientific/medical presentations, e.g. scientific conferences, high-level scientific or business audiences

• Oversee and interpret new scientific data, literature, competitive trends and product opportunities and adjust medical and educational activities accordingly.

• Maintain and develop strong relationships with local scientific societies and central decision makers at relevant health authorities.

• Identify, develop and maintain collaboration with current and future Key Opinion Leaders

• Drive, coordinate, support and ensure regular follow up of medical -, investigator initiated and other research projects, including driving approval processes.

• Support to all company sponsored clinical trials. Ensure high scientific level of expertise within therapeutic area

• Drive organization and implementation of Advisory Boards and other scientific meetings

• Address adequately all unsolicited medical questions according with all applicable regulations and internal policies.

• Participate in relevant congresses, symposia's and other meetings.

Profile

• Pharmaceutical industry experience

• Experience in communication with medical authorities, hospitals, physicians /specialists and KOLs as well as other healthcare sector professionals.

• Experience in interpretation and dissemination of scientific and clinical data

• Excellent communication and presentation skills.

• Ability to work well in both a team environment and independently.

• Strategic mind-set whilst being target-oriented and results-driven, with an understanding of short and long term goals.

• A successful track record of developing relationships with patient organizations and other key stakeholders is highly valued.

• Team player and strong interpersonal skills.

• High initiative and problem solving skills.

• Ability to coordinate, manage and prioritize resources and workload in a busy professional environment.

• Balanced, yet structured, and fast in decision making processes.

• Ability to work in a professional and international environment, and understands and applies to the explicit corporate standards, practices and code of conduct.

• Professional and mature projection, and self-confident behavior.

• Business proficiency in English

Desirable Skills and Experience

• Preferably a proven track record with phase 4 studies and Investigator Initiated projects.

• Preferably experience with compliance practices and knowledge of drug safety and regulatory affairs.

Essential Qualifications

• At least Master level degree in medicine or other life science

• Preferably a PhD degree in medicine, or other life science

• Preferably a Medical Doctor degree

• Preferably knowledge of the client relevant therapeutic areas

Job Offer

• Assignment for 6 months *could be extended with 3 months