Medical Science Liaison

Location:  remote, France Category: Medical Affairs

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Description

Who We Are

For more than two decades, going our own way has led to countless breakthroughs, bettering the lives of those suffering from rare genetic disease. In 1997 we were founded to make a big difference in small patient populations. Now we seek to make an even greater impact by applying the same science-driven, patient-forward approach that propelled our last 25 years of drug development to larger genetic disorders, as well as genetic subsets of more common conditions. Through our unparalleled expertise in genetics and molecular biology, we will continue to develop targeted therapies that address the root cause of the conditions we seek to treat. Applying our knowledge to make a transformative impact is not just a calling, but an obligation to those who will benefit most. The end goal has always been better lives and now we can reach more.

And the more people we reach, the more our impact can grow. We transform lives through genetic discovery.

Our Culture

Our desire to make a positive impact on our patients extends to our employees and BioMarin is committed to fostering an inclusive environment where every person feels seen, valued, and heard – so employees can thrive in all areas of their lives, in and outside of work. We seek to provide an open, flexible, and friendly work environment to empower people and to provide them with the ability to develop their long-term careers. Ultimately, we want to be an organization where people enjoy coming to work and take pride in our efforts to help patients.

BioMarin’s Research & Development group is responsible for everything from research and discovery to post-market clinical development. Research & Development involves all bench and clinical research and the associated groups that support those endeavors. Our teams work on developing first-in-class or best-in-class therapeutics that provide meaningful advances to patients. Come join our team and make a meaningful impact on patients’ lives.

Job Description

Medical Science Liaison (MSL) is the external-facing scientific expert on the company product(s) and therapeutic area(s), with the core responsibility of scientific engagement. This consists of the establishment and maintenance of ethical and highly scientific peer to peer relationships with leading Health Care Professionals (HCPs) at major academic institutions and hospitals. Based on high-quality interactions and on the generation, interpretation, and communication of scientific data with leading HCPs, MSLs could potentially improve - through meaningful scientific exchange - the clinical management of patients and their quality of life.

Tactics of MSL activities are aligned with BioMarin Medical Strategy and guided by BioMarin Medical Director according to Medical Plan.

Responsibilities

1)     Scientific engagement

  • Scientific engagement with Key Opinion Leaders (KOLs) in healthcare, academia, payers, and government organizations (as required), to provide appropriate scientific information about company products and related therapy area, gather insights and expert opinions from relevant HCPs. Thus, becoming a trusted scientific partner by enhancing the understanding of the scientific and medical value of BioMarin products
  • Proactive KOL / treatment centre mapping and planning according to the scientific strategic needs of the product or therapeutic area
  • Interactions with Patient Advocacy Groups to collaborate on unmet needs, educational needs and medical/scientific projects. Reactive provision of information to local Patient Advocacy Groups (PAGs) in lieu in line with Business Code of Conduct in collaboration with Patient Advocacy
  • Development and implementation of Scientific Exchange meetings at hospital, regional or national level. Support the France Medical Director/ TA Lead, on the development and implementation of local Scientific Educational Programs in line with BioMarin’s scientific needs, including the scientific briefing of the speakers
  • Conduct drug administration (dosing and administration) readiness trainings upon request
  • Support institution site readiness and perform on site drug risk-management drug education/information of post-marketing studies as required
  • Support post-marketing studies as required, in collaboration with study management
  • Scientific conference support
  • Responds to costumer requests with relevant scientific information and coordinate with Medical Information the provision of answers for on- or off-label queries

 

2)     Evidence generation support

  • Identify the evidence generation needs in the country
  • Prepare Evidenced Generation Proposals based on the local evidence generation needs
  • Support cross-functional team preparing the protocol and other needed documentation for local studies
  • Work with investigators in company sponsored studies supporting (by request) Clinical Operations and/or Study Management resources by sharing insights on potential study sites in alignment with France Medical Director / TA Lead, based on their scientific capabilities, administrative readiness, and stakeholder interests, partnering with clinical operations and Contract Research Organizations (CROs), as required, engaging with investigators both during start up and throughout the study period to maintain interest in and education about the study
  • Work with potential investigators clarifying the process of handling of independent research requests, aligned with BioMarin’s strategy and procedure
  • Reactive support to HCPs for assistance in providing scientific information to improve healthcare quality and effectiveness initiatives
  • Identify further scientific research opportunities in the area that help increase disease awareness, sharing of best practices, and identification of medical gaps and unmet needs.

 

3)     Insight management

  • Gather and regularly share insights and knowledge from HCP interactions with cross-functional team members
  • Identify unmet medical needs and feedback the corresponding insights to the organization so they can be actioned accordingly by the relevant party
  • Collect insights to understand current healthcare practices and treatment of patients with specific disease (e.g., patient and treatment journey)

 

4)     Medical strategic planning

  • Under supervision of France Medical Director contribute to strategic medical plans for the country as a part of integrated brand plan.

 

5)           Internal partnerships

  • MSL is an integral part of the BioMarin team, proactively coordinating activities with other field-based (Sales and/or Access Managers, Clinical Research Associates (CRAs), amongst others) and regional/global colleagues.

 

 

Expected level of competences

Core Competences

Level

Technical Competences

Level

Communication and Collaboration

Advanced

Scientific Strategy

Foundational

Leadership

Foundational

Medical Engagement

Advanced

Strategic Thinking and Planning

Foundational

Insight Generation

Advanced

Problem Solving and Decision Making

Foundational

Internal and Cross-functional Partnerships

Advanced

Adaptability and Flexibility

Foundational

Knowledge, Evidence Generation

Foundational

 

Education, Qualifications & Experience

•            In agreement with French exigences the requirement is a Master 2 or Engineer in a scientific or medical field at minimum.

•            Industry and field experience, ideally in rare diseases.

•            Understanding of the healthcare system and medical legislation in France.

•            Good written and oral English

•            Willingness to travel approx. 60% of time (including international travel).

Key Relationships to reach solutions

Internal

External

·       Cross-functional team in the countries and area

·       Senior Management within Brand or Disease area

·       Global and Regional Medical Affairs Function

·       Regional Market Access

·       Clinical Operations

·       Compliance Team

·       Healthcare professionals

·       Regulatory bodies

·       Medical Associations & Societies

·       Patient Advocacy Groups

·       Service Providers

·       Other local and regional stakeholders

 


We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law.

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