Medical Science Liaison - Oncology Budapest

Medical Science Liaison - Oncology
Budapest

Your new company:

We are looking for a Medical Science Liaison to our innnovative pharmaceutical partner company. Your responsibilities:

Represent Medical Affairs as subject matter expert in the assigned TA and territory, provide scientific and technical leadership to ensure professional and credible relationships with external experts /HCPs of strategic importance.

Serve as a point of contact within the Medical Affairs team for external experts within the assigned therapeutic area to satisfy their needs for scientific knowledge in a therapeutic area and, when requested, relevant medicines, to support their safe, effective and appropriate use.

Develop and execute scientific interaction plans, contribute to cross-functional account planning, as appropriate.

Responsible for appropriate tiering and segmentation of external experts based on guidance from the IFT playbooks and appropriate documentation of HCP interactions and relevant insights in the CRS and related platforms and systems.

Ensure a strong medical and scientific presence in biologic therapy centers by facilitation of research and educational initiatives, while supporting requests for medical and scientific information on products or areas of therapeutic interest.

Support internal teams such as sales and marketing and members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific update presentations. Work collaboratively and cross-functionally with other in-field members while retaining functional independence.

Assist in the initiation, oversight and follow up of assigned GMA studies and medical projects initiated within the therapeutic area for which the MSL carries responsibility (e. g. registry/database projects, epidemiological studies, post-authorization studies (PMOS)

Support prioritized interventional studies run by Clinical Development Operations, with study initiation visits and act as subject matter expert as part of One R&D community. All such activities must comply with applicable local laws, guidelines, codes of practice, SOPs, and R&D SOPs.

Act as the point of contact with external experts to facilitate investigator-initiated study (IIS) ideas and requests for support to the local and global medical teams as appropriate.

Attend relevant scientific meetings and Conferences. Collaborate with internal stakeholders to develop summaries of key data and other scientifically relevant information to inform strategic priorities and initiatives.

Upon request, assist physicians with requests for access to medicines on a named patient or compassionate use basis, subject to all applicable legal and regulatory requirements.

Provide key thought leaders / external experts and internal medical and clinical teams with scientific and technical support for publications of scientific or medical interest.

Ensure that all activities and interactions are conducted with due regard to all applicable local, global, and national laws, regulations, guidelines, codes of conduct, Company policies and accepted standards of best practice.

What you need to succeed:

Advanced degree (MD or PharmD).

Experience in the assigned TA is an advantage but not a basic requirement.

Experience working in pharmaceutical industry with general knowledge on ways of working in the industry, drug development/clinical research, market access environment, local laws, and regulations.

Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives of a pharmaceutical company.

Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research.

Ability to comprehensively learn about new subject areas and environments.

Excellent written and spoken communication and presentation skills in English and in Hungarian, with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians, and other healthcare decision makers.

High customer orientation.

Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity.

Driving licence

What you can expect from our partner:

Competitive salary

Bonus

Cafeteria

Company car

Innovative company culture

Opportunity to improve

What you need to do now In case you find this opportunity interesting, press on the ’Apply’ button and send us your fresh CV.