Medical Affairs Scientist Rare Disease - Early Lazio

Medical Affairs Scientist Rare Disease - Early
Roma
Lazio, Lazio

This is an exciting time to join Pfizer, an innovative biopharmaceutical company, one of the most admired companies in the world this year, and becoming a household name along with the COVID-19 vaccine.

The company is transforming into a science powerhouse, has many new launches ongoing and planned in several therapeutic areas.

At the same time we are considerably increasing our organization's digital skills in line with the evolving environment.

Pfizer Italy footprint is strong, we have over 2. 000 colleagues in our commercial, international and manufacturing operations.

The focus of the Rare Disease group is to transform thousands of patients and families lives by working together collaboratively to create innovative programs that serve the rare disorders patient community.

Pfizer is hiring a Passionate, Talented, Innovative, Charismatic Medical Affairs Scientist (MAS) responsible for Early pipeline in Rare Disease (RD) Medical Affairs Department.

The hiring of the MAS RD, Early Pipeline fits the iTALent purpose, providing a rare growth and development opportunity to lead scientific innovation in our Rare Disease Therapeutic Areas.

The MAS Early Pipeline will report to the Italy Rare Disease Medical Director.

Why Patients Need You

The Medical Affairs Scientist RD, Early Pipeline is an integral member of the Rare Disease (RD) Italy Medical Affairs organization.

The RD category has been developed to maximize the existing in-line portfolio in hemophilia, acromegaly and other endocrine disorders, ATTR Amyloidosis while positioning Pfizer as a rare disease category leader with an exciting and promising pipeline, including a gene therapy ("GTx") manufacturing and technology platform.

The MAS RD, Early Pipeline, combines the medical expertise and understanding of the patient's and physicians' point of view with that of the Therapeutic Areas and the relevant medicine(s).

He/she is a part of a working environment where colleagues always understand and exhibit customer-focused medical professionalism with honor and integrity while putting the patient first within the spectrum of the Pfizer Core Values and Leader Behaviors.

- Key Experience Offer of this Role

- MAS is the medical scientific companies' POC for HCPs, medical societies, regulators, academia investigators participating in Pfizer sponsored studies and other external scientific stakeholders.

- Early Pipeline MAS works to facilitate dialogue about Pfizer investigational products, and compounds in development, establishing a strong collaborative scientific relationship through non-promotional activities such as scientific exchanges (e. g. , discussion using the latest research papers and follow-up of contents of academic conference presentations) with relevant stakeholders in the assigned area.

- The MAS will play a central role as a scientific leader though identifying unmet medical needs, building medical plan and establishing evidence.

- Early Pipeline MAS also participates in close partnership with affiliate-based CSM (clinical site management) staff in the initiation, oversight and follow-up of clinical studies.

- Primary Responsibilities- Provide medical affairs leadership to the clinical development and registration process of pipeline compounds in the relevant TA, maintaining the highest scientific standards during in / external activities to provide deep medical and scientific expertise. -

- Establish deep and enduring peer-to-peer scientific relationships with leading healthcare professionals and key decision makers to develop beneficial solutions for RD early pipeline products under responsibility that enhance patient care. -

- Serve as a reliable, trusted resource of accurate, current medical and scientific knowledge in the therapeutic area, including competitive medicines, for internal and external stakeholders and customers. Collaborate with Global Medical Affairs, and as appropriate, Commercial Development, Clinical Development, research, and other cross-functional teams in supporting strategic direction for respective pipeline assets and TAs as well as for lifecycle plans, and Global/Local plans-

- Contribute to the preparation and execution of local medical operating plans for the pipeline products on the basis of identified local needs, insights and opportunities to address unmet medical needs and fill data gaps in the assigned products and therapeutic areas-

- Hold and effectively manage the medical affairs budget for early pipeline products under responsibility. -

- Establish and maintain a close working relationship with CSM (clinical site management) staff and partner in facilitating the initiation and conduct of Pfizer-led clinical trials in country. - What You Offer

BASIC QUALIFICATIONS- Medicine degree is required, specialty training or PhD is strongly preferred-> 3 years industry or academic experience or clinical experience is required- Knowledge of clinical development processes- Ability to objectively interpret and anal