Main Responsibilities / Duties
To provide deep medical & scientific expertise to support healthcare professionals, professional associations, patient groups and other relevant decision makers. This includes the following:
Partnerships
To provide medical & scientific expertise to healthcare professionals, professional associations, patient groups and other relevant decision makers through scientific communications
To establish Pfizer as a key research partner within National Life Sciences by building academic and research collaborations within the nominated therapy area
To establish deep and enduring peer-to-peer relationships with leading healthcare professionals and specialists, including non-traditional partners and key decision makers
To understand clinicians' insights around current standard of care and strengthen their knowledge of the value of our medicines to the patients and decision makers
To liaise with healthcare professionals to effectively communicate and manage drug safety issues
To provide specialist medical and scientific input to the nominated internal teams in order to support the appropriate use of Pfizer medicines and successful implementation of Pfizer's initiatives and programs
Data Generation and Publications
To identifies data gaps for pipelines assets and develops local RWD/RWE for the demonstration of the value of our products and market access.
To acquire and maintain in-depth scientific expertise of Pfizer medicines within nominated therapy area as well as of key competitors (including those in development)
To deliver key medical and scientific activities within the medical plan, e.g. high-quality educational materials, generation of real-world evidence, non-interventional studies, database studies and registries (in collaboration with the Health & Value team) and ensure timely publication of data
To provide medical expertise to evaluate requests to support medical education, quality improvement, health services research, investigator sponsored research (ISR) and clinical research collaborations
Clinical Development
To provide medical/scientific input into protocol feasibility assessments for clinical trial proposals
To identify appropriate investigators / sites for Pfizer-sponsored clinical trials
To work together with clinical research colleagues and in collaboration with global teams to drive the timely completion of Pfizer-sponsored clinical trials
To provide input into clinical development teams to ensure design and selection of trials relevant to Turkey needs, leveraging clinician, payer and patient insights
To effectively implement approved compassionate use and named patient supply programs to ensure appropriate access to Pfizer medicines in response to clinician requests
Data Communication and Medical Insights
To present high-quality, accurate, balanced and specific information to healthcare professionals and other relevant decision makers in response to unsolicited requests for information
To create industry leading and impactful scientific and medical content through a range of digital channels and formats that is timely, relevant, balanced, interactive, innovative and easily digestible. This may include videos, webinars, interactive pdfs, peer reviewed publications, congress materials, clinical trials and real-world data
To ensure medical insights are brought into the organization to shape future strategies
To lead local advisory boards to gain clinical and patient insights
To work with patients and patient organizations to understand unmet medical need and to ensure the patient voice is at the center of medical strategies and projects
To present the medical perspective on selected topics during media briefings
To provide scientific insights and support to field and head office based commercial colleagues
To review and approve (where applicable) medical materials and activities within scope of the MoH, AIFD and company codes
Cross Functional Medical Activity
To provide medical expertise into regulatory and market access strategies for pipeline assets, including early licensing & access schemes, regulatory and HTA submissions and adaptive pathways
To provide medical expertise for regulatory labelling updates, risk management plans and license maintenance
To provide clinical input to Medical Information to facilitate the maintenance of an accurate, relevant and high-quality database of standard response documents/creation of new responses
To develop and maintain strong cross-functional working between global and local country teams
To identifies opportunities for customer focused digital solutions and contributes to their creation in partnership with MAS/Digital Medical.
To perform the medical customer facing activities for the assigned products, according to the priorities defined with the Manager, and liaises with the other medical colleagues, if applicable
To review and sign-off to ensure compliance of promotional materials and company sponsored activities such as local promotional meetings and events with local SPCs and requirements.
To work closely with the MAEL, MAS/Digital Medical, the MAS/Real World Data Expert, the Medical Quality Governance Manager (MQGM), Compliance, Legal and all cross-functional team, including customer-facing roles
Required Skill Set
Technical
Understanding in the following areas:
o Medical plans and budget management
o Medical governance and cross-functional teams' collaboration
o Medical writing and comprehensive medical review of documents
o Communication skills to different stakeholders and across different channels
o External engagement competencies, including networking and stakeholders mapping & management
Performance driven with professional demeanor and strong collaboration skills
Ability to focus on priorities, resilience, organization, and project management competencies
Sense of responsibility and accountability, quality orientation
Strategic, agile, innovative and growth mindset
Language Requirements: Fluent in Turkish and English
Personal skills:
Performance driven with professional demeanor
Ability to lead complex projects with multiple external and internal stakeholders
Business acumen and high level of industry understanding
Customer oriented mindset
Ability to act in midst of uncertainty
Self-management & ability to manage heavy workload
Experience in setting up networks and develop them
Excellent communication skills
'Can do' & pioneering attitude, solution driven
Sense of responsibility and accountability, quality orientation
Managerial: N/A
Certifications:N/A
Education:
Medical Doctor or Pharmacist with Ph.D.*
(*Exceptional situation for the latter educational requirement does not apply to those colleagues who are Pharmacists only and who already hold a similar Medical Affairs position internally)
Experience:
Pharmaceutical industry experience within medical affairs
Good knowledge of the national healthcare and medicine funding/reimbursement systems
Knowledge of health economics, pharmacovigilance and regulatory affairs
Experience in RWD/RWE generation in healthcare
Experience in clinical research
Work Location Assignment: Hybrid
Purpose
Breakthroughs that change patients' lives… At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.
School of Leaders
We, as Pfizer Turkey, make a difference with our visionary and pioneering approaches ranging from our concept of raising leaders through rotations, providing international career opportunities to creating a flexible, enjoyable work environment. There are no limits to what we can accomplish to touch lives here!
Flexibility
We aim to create a
Tagged as: Life Sciences
Medical Affairs Specialist Main Responsibilities / Duties To provide deep medical & scientific expertise to support healthcare professionals, professional associations,...
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