MSR Oncology Hematology(Andalucía)

Posted Yesterday
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9 Locations
In-Office
Entry level
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Develops scientific partnerships with oncology and hematology key opinion leaders, executes local medical plans, communicates clinical evidence, supports clinical research and post-marketing studies, and provides scientific input to internal teams. The role disseminates Pfizer medicine data, supports investigator-sponsored research, trains commercial colleagues, attends scientific meetings, and ensures compliant medical communications. This field-based position covers Andalusia and requires travel, English fluency, health sciences education, and a European work permit.
Summary Generated by Built In
Job Description
Medical Affairs Scientist /Medical Scientific Relations (MAS/MSR) function is responsible to create scientific partnership with local KOLs through a qualified approach that results in access and advocacy based on scientific evidence.
In addition, he/she is the point of accountability for medical and scientific issues and initiatives related to therapeutic area.
Medical Affairs Scientist / MSR (MAS/MSR) is accountable for developing and executing the country medical plan at local level that supports the strategic operating goals for the business.
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.
  • Be the in-field medical expert in the area of hematology tumours
  • Facilitate medical and scientific field intelligence, to know investigators/potential investigators, understand competitive research activities in active or planned study sites, generate insights from investigators and identify opportunities for collaborations with key institutions and KOL leaders at local level
  • Plans and executes local medical scientific strategic plans, as per their specialty role. Provide in country support for therapeutic areas. 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
  • Observation and assessment of competitor drug
  • Attend relevant scientific meetings and Conferences
  • Lead medical to medical communications in the field
  • 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.
  • Ensure that new clinical data on Pfizer medicine are promptly disseminated in the most accurate manner, compliant with the label of the product.
  • Ensure a strong medical and scientific presence for Pfizer in investigational sites and key scientific centers:
  • Provide scientific and technical leadership to ensure professional and credible relationships with investigators
  • Internal discussion of research grants proposal with above country medical team
  • Provide support for adequate independent sponsored research, non-interventional studies and research grants planning and management.
  • Facilitation of clinical research and interventional phase 1-4 trials with Pfizer drugs.
  • Management of post-marketing studies (clinical trials, observational /pharmacoepidemiological studies
  • Work in close collaboration with internal colleagues
  • Support promotional activities on regional KOLs and Scientific Societies including active preparation and participation in symposia, opinion leaders' meetings and advisory boards
  • Aligns, supports and contributes to different internal stakeholders.
  • Support internal training of customer facing commercial colleagues, enhancing their knowledge, and understanding of clinical data and our medicines
  • Provide scientific input to the cross functional team and contributes to company's plans through actionable customers' medical insights.
  • Keep internal activities, field interactions, and M2M communications correctly tracked through periodic reports
  • Ensures conduct all of work in compliance with Pfizer internal policies and European / local regulation, codes of conduct and accepted standards of best practice in all activities and interactions (research, communications, unsolicited queries on off label use of drugs, ...)

Education, Skills and Professional Experience
  • Degree in Health Sciences
  • MD, MBA, PhD and/or expertise in Oncology strongly desired.
  • Previous experience as MSL/MSR desired, and Oncology/hematology local environment knowledge preferred
  • Fluency in English required
  • Background/clinical experience with Epidemiology, Oncology, Immunology, Clinical Trials, molecular biology, translational medicine preferred
  • Excellent interpersonal, written and verbal, communication skills (scientific and non-scientific)
  • Previous experience in medical writing, submission of papers to peer review papers
  • Strong customer orientation, science based
  • Project management skills and capacity to work under strict deadlines
  • Demonstrated ability to effectively work in a multi-functional team and good teamwork spirit
  • Demonstrated ability to rapidly adopt and utilize new digital technology and other resources with medical customers and record medical interactions
  • Working knowledge of Regulatory Affairs, Drug Safety, Legal and compliance
  • Computer skills
  • Interest and knowledge on innovation, as artificial intelligence (AI), digital environment, statistics...
  • Willingness to travel as it is a field-based role. Possesses valid driver's license

Ideally, you also have:
  • Good understanding of the local healthcare environment at national and regional level
  • 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

Additional Information
  • Type of position: Full time, regular
  • Regional-based; position based in Andalusia
  • European work permit necessary
  • NO Relocation package available
  • Please send CV and cover letter in English

#LI-PFE
This role is posted in multiple locations. If you are applying for the role in an secondary job posting location where pay transparency regulations apply, your Talent Advisor will share the local pay information with you during the first interview.
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.
Digital Transformation Strategy
One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.
Flexibility
We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let's start the conversation!
Equal Employment Opportunity
We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms - allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.
Disability Inclusion
Our mission is unleashing the power of all our people and we are proud to be a disability inclusive employer, ensuring equal employment opportunities for all candidates. We encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments to support your application and future career. Your journey with Pfizer starts here!
Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email [email protected]. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned.
Se valorarán las candidaturas que puedan aportar certificados oficiales de discapacidad.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Medical

Skills Required

  • Degree in Health Sciences
  • Fluency in English
  • European work permit
  • Valid driver's license
  • Willingness to travel in a field-based role
  • Excellent interpersonal, written, and verbal communication skills
  • Ability to work effectively in multifunctional teams
  • Ability to work under strict deadlines and manage projects
  • Computer skills and ability to adopt digital technology
  • Working knowledge of Regulatory Affairs, Drug Safety, Legal, and compliance
  • MD, MBA, PhD, and/or oncology expertise
  • Previous MSL or MSR experience
  • Local oncology and hematology environment knowledge
  • Clinical experience in epidemiology, oncology, immunology, clinical trials, molecular biology, or translational medicine
  • Medical writing and peer-reviewed paper submission experience
  • Knowledge of innovation, artificial intelligence, digital environments, and statistics
  • Understanding of local healthcare environments
  • Knowledge of pharmacovigilance and regulatory legislation
  • Understanding of drug development and clinical research processes

What the Team is Saying

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Esteban
Pfizer
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The Company
HQ: New York, NY
121,990 Employees
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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