Medical Affairs Intern
Secteur : Industrie du médicament humain Famille de fonction : Information médicaleDescription du poste et des missions
Company description
Recordati Rare Diseases (RRD) is a unique pharmaceutical company focusing on patients affected by life-threatening conditions and specialized in bringing orphan drugs to market for rare diseases.
We are committed to improving the diagnosis and management of these diseases by strengthening collaboration and building expert networks.
Patients and their families are central to our planning, our thinking and our actions.
Position Summary
We’re looking for a Medical Affairs Intern with scientific, clinical and therapeutic area knowledge or interest, supporting our Global Medical Affairs Manager for Dermato-oncology RRD product, including medical information, scientific review for medical and promotional materials, and Investigator initiated Studies (IISs)/collaborative research proposals.
Our internship offer is subject to the possibility of signing an internship agreement with the selected student's university.
Key Duties and Responsibilities
- Support in building and managing the medical information capabilities for Dermato-oncology Recordati rare diseases products
- Support in clinical development communication with a focus on data quality, compliance and timely responses
- Support in creating and maintaining a product knowledge database including, but not limited to, written standard response letters and FAQ documents that are scientifically accurate and fair-balanced
- Support to the medical affairs reviewer for promotional and non-promotional scientific materials, and the management of the IIS/collaboration research and expanded access/compassionate use program(s)
- Support in planning and managing medical-scientific events, symposia, advisory boards (e.g. KOL selection, meeting materials, and logistics)
- Support to the Medical Affairs Manager at major scientific meetings and conferences, staff conference booths and development of meeting reviews/reports as assigned.
- Perform subject-specific literature reviews to assist the organization in staying abreast of the scientific landscape and developments
- Support in implementing policies, SOPs and work instructions governing the operations of medical affairs to meet all compliance standards and regulations
- Support in establishing strong collaborative relationships with key internal and external stakeholders
- Other duties as assigned
Profil souhaité
- Advanced degree: PhD, PharmD, or MD
- Excellent communication, written, verbal and presentation skills
- Proven ability to review, interpret and present complex scientific data
- Analytical and problem-solving skills; detailed oriented, independent and critical thinker
- Ability to shift priorities while working under deadlines,
- Must have excellent customer-service orientation,
- Ability to foster and maintain professional relationships
- Project planning skills
- Fluent in English