Role Description + The Medical & Scientific Liaison (MSL) function is responsible to create scientific partnership with local KOLs through a qualified approach that results in access and advocacy based on scientific evidences.
The MSL is accountable for execute the medical to medical communication plan that supports the strategic operating goals for the business.
Advice and scientific support to HCPs and Stakeholders panel, including physicians, researchers and opinion leaders, assuring compliance with the Pfizer and governance policies.
MSL will be in charge of delivering updated scientific information to all healthcare professionals.+ Primary purpose is to establish and maintain peer-peer relationships and scientific exchange with leading physicians, referred to as Key Opinion Leaders (KOL's), at major academic institutions, societies, Hospitals and cancer centers.
MSL will have a constant interaction cross functional with different members of the BU and areas. Main responsibilities : + Develop and consolidate a network of relationships with the KOL and Scientific Institutions at the local level, sharing the wealth of knowledge and technical skills in order to support the scientific and medical leadership of the company+ Disseminate scientific information to scientific community through 'Medical to Medical communication' (individual meetings and group), in line with company procedures+ Preparation of scientific talks and presentations.
Manage in a way compliant with laws and Pfizer policy, the unsolicited queries on off label use of drugs+ Promote to KOLs medical activities developed at the central level (e.
g. medical education programs, congress, among others) to support the implementation of scientific strategies in their own territory.
Ensure that new clinical data on Pfizer medicine are promptly disseminated in the most accurate manner, compliant with the label of the product+ Be the in-field medical expert in the area+ Support internal training of customer facing commercial colleagues, enhancing their knowledge and understanding of clinical data and our medicines.
Observation and assessment of competitor drugs.+ Keep internal activities and field visits correctly tracked through periodic metric reports+ Ensures conduct of work in line with compliance regulations.
Support on Identify potential investigators and centres, Clinical trials (local, IIR's, RWD) : + Active preparation and participation in symposia, opinion leaders meetings and advisory boards.
Provide support for adequate IIR / NIS studies / Research grants planning and management+ Internal discussion of RG / IIRs proposal with above country medical team.
Management of post-marketing studies (clinical trials, observational / pharmacoepidemiological studies) to ensure that are in compliance with internal policy and local regulation REQUIRED SKILL SET + Medical or scientific qualification (Ph.
D. or Pharm.D.) M.D. preferred.+ Medical tranning or clinical experience in the therapeutic area desirable+ Desirable : Industry experience+ Education, Skills and academic Experience+ Master in the Pharma Industry, Biotechnology or others desirable+ Proven experience in a pharmaceutical / biotechnology company within a MSL or similar role desirable+ Background / experience with Inflammation field or Biological products desirable.
Working knowledge of Regulatory Affairs, Drug Safety, Legal and compliance environment+ Strong customer orientation, science based+ Excellent written and verbal communication skills (scientific and non-scientific)+ Willingness to travel as it is a field-based role.
Possesses valid driver's license+ Strong project management skills and capacity to work under strict deadlines+ Previous experience in medical writing, submission of papers to peer review papers preferred.
Demonstrated ability to effectively work in a multi-functional team+ Computer skills OTHER KNOWLEDGE, SKILLS AND HABILITIES : + Fluency in English (both written and spoken)+ Audience Management+ Oriented to business+ Technical Management in Microsoft office+ Good understanding of the local healthcare environment+ Knowledge of the relevant and applicable Codes of Practice and conduct such as FCPA, SOPs, regulations and guidelines as they apply to the function Good understanding of drug development, clinical research, medical decision making and health environment+ Good knowledge of pharmacovigilance and regulatory legislation and how it impacts the product portfolio+ Good knowledge of drug development processes+ Good understanding of Clinical Research+ Knowledge of Health Economics, Pharmacovigilance and regulatory legislationEn Pfizer, tenemos el objetivo de ser tan diversos como los pacientes y las comunidades a las que servimos, a través de una cultura vibrante y enriquecida por la mezcla de nacionalidades, identidades, experiencias, tradiciones & capacidades.
Estamos comprometidos con atraer Talento basándonos en las habilidades y experiencias imprescindibles para realizar el trabajo.
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Traé tu auténtico ser al trabajo - Bring your authentic self to work - #LI-PFEPfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Medical