Job type: 100%, Temps de travail : 90-100%

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About AbbVie

We are a global, research-based biopharmaceutical company focused on the discovery and development of innovative treatments that address some of the world’s most serious and complex diseases. We strive to have a remarkable impact on people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology and gastroenterology. In addition, AbbVie offers products and services through its Allergan Aesthetics portfolio.

AbbVie with headquarters in Chicago, USA, employs approximately 50,000 employees worldwide and is celebrating its 10th anniversary in 2023. Around 57 million patients in more than 175 countries benefit from AbbVie medications annually. Approximately 250 employees are employed in Switzerland and the AbbVie Switzerland headquarters are located in Cham, ZG. For more information, visit our website: www.abbvie.ch


Job Summary

The Medical Science Liaison serves to advance science and standards of care for patients, healthcare providers and payers, and ensure they can access all the practical and clinically relevant information and solutions they need to use AbbVie’s products efficiently and safely. The field-based Medical Science Liaison focuses on medical and scientific engagement with AbbVie stakeholders (including research and healthcare professionals, payers, and providers).

KEY RESPONSIBILITIES:

  • Provide information to customers and facilitate dialogue about AbbVie’s marketed products, and compounds in development, in a strictly scientific, non-promotional manner, and in full compliance with applicable national laws and regulations, guidelines, codes of conduct, AbbVie’s policies and procedures and accepted standards of best practice.
  • Enhance the scientific credibility of the Company with established and emerging National and Regional thought leaders, by supporting scientific dialogue and collaborations in the areas of research, medical and scientific exchange, including facilitation of requests for scientific and medical information.
  • Interface with other key members of the affiliate medical department and work collaboratively and cross-functionally with other in-field team members while retaining functional independence.
  • Maintain a high level of scientific knowledge to ensure credible dissemination of scientific information and informed scientific dialogue with thought leaders, healthcare providers and payers.
  • Provide scientific and technical input to local AbbVie Brand teams and external thought leaders using information that has been reviewed and approved by relevant local procedures, and under the direction, governance and oversight of the MSL’s manager, therapeutic area Medical Manager, or Affiliate Medical Director as appropriate. This includes working with local Medical Information teams, as appropriate, to respond to unsolicited requests for off-label information on AbbVie medicines.
  • Develop and maintain collaborative relationships with thought leaders in the product / therapeutic area for which the MSL has been assigned responsibility, to facilitate Abbvie research and educational priorities and strategic initiatives.
  • Ensure a strong medical and scientific presence for Abbvie in key academic centers by facilitation of research and educational initiatives, while supporting requests for medical and scientific information on products or areas of therapeutic interest to Abbvie.
  • Support internal teams such as sales and marketing and members of the Affiliate Brand Team to develop their scientific and technical expertise through the delivery of scientific update presentations.
  • Assist in the initiation; oversight and follow up of assigned clinical studies and medical projects initiated within the therapeutic area for which the MSL carries responsibility (e.g. post marketing clinical activities such as registry/database projects, epidemiological surveys, post-authorization studies (phase IV). All such activities must comply with applicable local laws, guidelines, codes of practice, SOPs, and AbbVie R&D (GPRD) SOPs.
  • Act as the point of contact with thought leaders to facilitate investigator initiated study (IIS) ideas and requests for support to the local and global medical teams as appropriate.
  • Serve as a point of contact within the. Medical Affairs team for thought leaders and external experts within an assigned geographic area in order to satisfy their needs for scientific knowledge in a therapeutic area and, when requested, relevant AbbVie medicines, to support their safe, effective and appropriate use.
  • Deliver credible presentations on scientific matters to physicians, individually or in groups (meetings, clinical sessions, etc.), where requested.
  • Participate in the selection process to identify appropriately qualified thought leaders the Company would wish to engage in collaborative efforts — such as potential research collaborations, or educational and advisory roles (Advisory Boards, Congresses, Symposia, etc.); while ensuring a high level of scientific or educational integrity in these collaborative efforts.
  • Facilitate medical and scientific field intelligence — for example, competitor research and medical strategies, educational activities — and communicate, where appropriate, within the Company.
  • Assist physicians with requests for access to AbbVie medicines on a named patient or compassionate use basis, subject to all applicable legal and regulatory requirements.
  • Ensure that all activities and interactions are conducted with due regard to all applicable local, global and national laws, regulations, guidelines, codes of conduct, Company policies and accepted standards of best practice.

QUALIFICATIONS AND EXPERIENCE:

  • University degree (Masters and/or PhD preferred) in a relevant scientific discipline
  • First experience in developing and maintaining expert knowledge for an assigned therapeutic area, and in medical research in general preferred
  • Demonstrated expertise in the scientific methods applied to clinical research and current legislative/regulatory controls applicable to this research
  • Ability to comprehensively learn about new subject areas and environments
  • Excellent written and spoken communication and presentation skills, with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians and other healthcare decision makers
  • High customer orientation
  • Strong commitment to compliance with the relevant rules and procedures, and to scientific quality and integrity
  • Business fluent in English and French

CRITICAL SKILLS REQUIRED FOR THE ROLE:

  • Ability to comprehensively learn about new subject areas and environments
  • Excellent written and spoken communication and presentation skills, with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians and other healthcare decision makers
  • Ability to translate complex Medical topics into understandable messages for non-Medical staff


AbbVie is an equal opportunity employer including disability/vets. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a disabled veteran, recently separated veteran, Armed Forces service medal veteran or active duty wartime or campaign badge veteran or a person’s relationship or association with a protected veteran, including spouses and other family members, or any other protected group status. We will take affirmative action to employ and advance in employment qualified minorities, women, individuals with a disability, disabled veterans, recently separated veterans, Armed Forces service medal veterans or active-duty wartime or campaign badge veterans. The Affirmative Action Plan is available for viewing in the Human Resources office during regular business hours.

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Deadline: 19-05-2024

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