Junior Medical Advisor Specialty Care (Staff Leasing)
The position offers a permanent contract with an external agency.
Overview
As a Jr Medical Advisor Specialty Care you will be an expert for assigned product, providing scientific support within the therapeutic areas to internal and external stakeholders by fostering, cultivating and maintaining credible and unbiased medical and scientific dialogue, in order to ensure an effective presence in the company’s therapeutic area.
Responsibilities
- Support the implementation of scientific initiatives (advisory boards, digital activities, clinical, epidemiological, observational trials, etc.), following a strategical / tactical plan as for Brand Plan, meeting the timelines and costs and in compliance with Company\'s standards and the legislation in force.
- Collaborate with other members of medical affairs and cross-functional team to define and implement key strategic messages for medical communication and medical activities for therapeutic areas of competence, including digital editorial plans.
- Collaborate in developing and maintaining relationships with medical associations, external experts and other relevant stakeholders within the therapeutic area in order to optimize the scientific community\'s knowledge of products and development activities within the medical community.
- Ensure support in monitoring of trials falling within area of competence in order to assure scientific validity of results, as well as compliance with plans and ensure support for publication of national Trial results in scientific journal.
- Support in providing LRA with the scientific advice needed to draw up the documentation required by Regulatory Authorities.
- Ensure collaboration with Corporate Medical Affairs to define communication strategies and develop medical / scientific initiatives to ensure correct and compliant scientific communication about company products for the therapeutic area of competence.
- Participate in training for customer facing roles.
- Ensure that all interactions and engagements activities are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with BI values.
Requirements
- University degree in life sciences or related field; higher degree / qualification (e.g. MSc, PhD) would be a plus.
- Scientific Degree; Doctoral (MD) degree on Medicine is a plus but not mandatory.
- Solid medical / scientific background and previous experience in oncology, rare diseases or respiratory area is strongly preferred.
- Previous experience in new drugs launches is an advantage.
- At least 1 year of experience in pharma industry in similar roles.
- Fluency in English and Italian.
- Knowledge of the pharmaceutical industry processes.
- Knowledge of clinical research, clinical trial management (regulations and GCP).
- Highly customer focused with an awareness of the importance of business results.
- Relevant communication and negotiation skills.
Why Boehringer Ingelheim?
With us, you can grow, collaborate, innovate and improve lives.
We offer challenging work in a respectful and friendly global working environment surrounded by a world of innovation driven mindsets and practices. In addition, learning and development for all employees is key, because your growth is our growth.
To learn more about what benefits could be waiting for you, please visit our Career area.
Job Details
Job - Medicine / Regulatory Affairs
Primary Location - Europe-IT-Lombardia-Milano
Organization - IT-Boehringer Ingelhem Italia SpA (Italy)
Schedule - Full-time