Position Code: MA_GUIDOTTI_2023
Guidotti Hellas (affiliate of Menarini Group) intends to recruit:
Medical Advisor
The candidate will be responsible for providing medical scientific advice for key company products.
The Main Responsibilities Include:
- Life-cycle management for products of responsibility
- Ensure excellent product knowledge and documentation (clinical studies of products and competition, international and national guidelines, HTA assessments and requirements).
- Organize and deliver scientific meetings for internal and external customers.
- Produce regular scientific competitive intelligence reports to help refine product strategies.
- Be present in the market to deliver scientific exchange with Key Opinion Leaders (KOLs) and Opinion Leaders (OLs) in the respective therapeutic areas, including medical-scientific presentations where applicable. Also liaising with key experts for the development of a set of unmet medical and scientific needs and clinical studies ideas (IITs, NIS etc.).
- Organize and deliver medical-scientific meetings, such as advisory boards, scientific Fora and other medical/scientific meetings.
- Participate in key congresses of the involved Therapeutic Areas (TAs), in Greece and abroad, as per the company’s and department’s policies.
- Cross-functional brand team work, including Marketing, sales force, market access and other relevant functions to ensure up-to-date and competitive promotional and non-promotional materials (including medical review and approval), strategic and tactical campaigns support, scientific training of involved functions.
- Support in all patient-related activities [e.g. Patient Support Programs (PSPs)], where applicable.
- Product launches
- Work with internal stakeholders to prepare the launch of new products, by ensuring latest and highest level of product medical/scientific knowledge, market dynamics understanding, competitive intelligence and unmet medical needs.
- Run advisory boards, small group and 1:1 meeting with key experts in the field to ensure best understanding of the medical and patient needs.
- Clinical trials support and responsibility
- Assume responsibility for local clinical trials in the respective therapeutic areas.
- Understanding for the unmet scientific needs and developing concepts for new evidence generation.
- Responsibility for contribution or self-development of clinical documents (protocol, CRF, ICF etc.).
- Assume responsibility as medical study manager, as per the company’s SOPs and Working Instructions (WI).
- Drive the publication record for the studies and conform to all relevant regulations and codes of conduct.
- Pharmacovigilance (PV) and Medical Information support
- Provide accurate and scientifically sound information to support Medical Information enquiries and examination of Adverse Events (AEs) reports.
- Assume responsibility for local clinical trials in the respective therapeutic areas.
Skills and Qualifications:
- University Degree in Medicine (desired specialty Pulmonologist), or other related health-sciences.
- Minimum 5-7 years of experience in the pharmaceutical industry, at least 2-3 in similar position.
- Able to interact on a peer level with key stakeholders internally and externally, KOLs and clinical investigators.
- Good understanding and command of concepts of medical writing, statistics and literature search.
- Highly effective communicator both orally and in writing.
- Excellent presentation and training skills.
- Able to work with confidence; self-driven, pro-active, extroverted and dynamic.
- Constant demonstration of a “can-do-attitude”, assuming responsibility and being results-oriented.
- Fluency in English / Fully computer literate.
- Demonstration of business acumen.
Remuneration
The company offers a competitive remuneration package and career prospects.
If you meet the above qualifications and believe that you can respond dynamically to the requirements of the position, please send us a curriculum vitae by entering the code position MED_2023 at hr@menarini.gr
All applications will be treated as confidential.