Medical Affairs Internship - Puteaux, France - Recordati Group
Description
Internship agreement details:
- Department : Medical Affairs
- Sector : Human pharmaceutical industry
- Location : Puteaux, HautsdeSeine (92), France (close to La Défense station)
- Type of contract : Internship
- Start date : April 1st 2024
- Duration : 6 months
- Remuneration : 900€ gross per month
- Benefits : 50% reimbursement of public transport subscription, lunch vouchers of €10 value (€4.71 per voucher paid by the intern, teleworking policy of 2 days per week
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.
Patients and their families are central to our planning, our thinking and our actions.
Internship Summary
The Medical Affairs Intern is providing support to the Global Medical Affairs Manager for Metabolics rare disease product, more specifically, focusing on organic acidurias (Carbaglu), NAGS deficiency (Carbaglu), cystinosis (Cystadrops and Cystagon), homocystinuria, (Cystadane) porphyria (Normosang), etc.
He/she is supporting the medical affairs activities including medical information, providing scientific review for medical and promotional materials, and reviewing Investigator initiated research (IIRs)/collaborative research proposals, advisory boards and expanded access program(s).
Key Tasks
- Support for the building and managing the medical information capabilities for Metabolic Portfolio Recordati rare diseases products. In details, organic acidurias (Carbaglu), NAGS deficiency (Carbaglu), cystinosis (Cystadrops and Cystagon), homocystinuria, (Cystadane) porphyria (Normosang), etc
- Support for the developement and communicating appropriate, quality, compliant and timely responses for Medical Information requests
- Support for the creating and maintaining a product knowledge database including, but not limited to, written standard response letters and FAQ documents that are scientifically accurate and fairbalanced
- Support for the medical affairs reviewer for promotional and nonpromotional scientific materials. Support for the building and management the IIR/collaboration research and expanded access/compassionate use program(s)
- Support for the planning, organization and managing medicalscientific events, symposia, advisory boards (eg. KOL selection, meeting materials, and logistics)
- Support the medical affairs representing Recordati rare diseases at major scientific meetings and conferences. Staff conference booths and support for the development of meeting reviews/reports as assigned
- Support implementation of policies, SOPs and work instructions governing the operations of medical affairs to meet all compliance standards and regulations
- Support for the establishment of strong collaborative relationships with key internal and external stakeholders
- Other duties as assigned
Essential Qualifications:
- Advanced degree: PhD, PharmD, or MD
- Disciplinary basic knowledge or interest in metabolic diseases
- Experience with expanded access programs is preferred
- Excellent communication, written, verbal and presentation skills
- Ability to review, interpret and present complex scientific data
- Analytical and problemsolving skills; detailed oriented, an independent and critical thinker.
- Customerservice orientation
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