Medical Science Liaison, Great Lakes

Galderma•Boston, OH

17h

About The Position

Galderma is the emerging pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that span the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ - the skin - meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. Because we understand that the skin, we are in shapes our lives, we are advancing dermatology for every skin story. We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. We aim to empower each employee and promote their personal growth while ensuring business needs are met now and into the future. Across our company, we embrace diversity and respect the dignity, privacy, and personal rights of every employee. At Galderma, we actively give our teams reasons to believe in our bold ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact. The Galderma Medical Science Liaison (MSL) serves as an internal expert to support the U.S. Nemolizumab team. The MSL develops and maintains professional relationships with external customers such as physicians and other health care providers (HCPs), nurse practitioners (NPs) and physician assistant (PAs) to provide comprehensive medical and scientific support for Nemolizumab in assigned areas of interest. The MSL will focus on providing HCPs, clinical investigators and professional organizations with proactive and reactive scientific information in a compliant manner. This Territory Includes: OH, MI, KY & W. PA

Requirements

Doctorate degree & 1-2 years of MSL/Medical Affairs experience preferred
Pharm.D., Ph.D., MD, or NP/PA
Three (3) plus years of clinical practice, clinical research, or medical research preferred.
Experience in a medically related field can include post-doctoral training (i.e., residencies and/or fellowships)
Excellent communication, presentation and time management skills required; must be adaptable, solution oriented and able to work well within a team and relate effectively with external HCP and internal stakeholders
Ability to interface effectively with a variety of technical platforms
Solid understanding of FDA, OIG, HIPAA, and other US regulatory principles
Current working knowledge of US legal, regulatory, and compliance regulations and guidelines
Ability to function with a sense of purposeful urgency in a team-oriented (matrix) environment
Strong scientific and/or clinical acumen
Strong business acumen
Demonstrated ability to organize, prioritize, and work effectively with a sense of urgency in an evolving environment
Superior soft skills and demonstrated credibility with medical professionals with ability to develop good relationship
Ability to complete expense reports in a compliant and timely manner.
Ability to manage travel in an organized and effective manner.
Travel is estimated at 70-80%

Nice To Haves

Dermatology or Immunology background preferred
Biologic and/or launch experience preferred

Responsibilities

Identify key opinion leaders and cultivate a network of experts
Drive Regional, National, and International External Expert and Influencer identification, tiering, and development in support for Nemolizumab.
Prepare and execute key opinion leader (KOL) engagement plans.
Develop, maintain, and execute US KOL and US Institution plans within respective geography.
Collaborate with health care professionals to identify opportunities for the development of algorithms and guidelines.
Execute qualitative and quantitative metrics required per the US medical affairs strategy.
Identify, collect and communicate medical insights and feedback gathered from scientific exchange and relevant information to define, update and support medical affairs strategies.
Conduct and implement a comprehensive disease awareness tactical plan within the respective geography by serving as an educational resource to healthcare providers on disease state concepts, including providing effective presentations to groups, and participating in 1:1 discussion.
Provide in-depth drug, mechanism of action and emerging clinical information to health care providers in the respective geography in a compliant manner.
Serve as a liaison to health care professionals and professional organizations and disease state advocacy groups.
Support the efforts of patient support groups and educational foundations.
Conduct discussions with HCPs to identify potential research gaps.
Identify and facilitate opportunities for data generation activities through proposals for posthoc analyses, Investigator-Initiated Trial (IIT), and Medical Affairs-sponsored studies for research that is aligned with Galderma’s strategic focus in a compliant and collaborative manner with home office colleagues.
Attend congresses, engage with external stakeholders, prepare congress summaries, and present key perspectives to internal stakeholders including competitor analyses.
Provide educational meeting support at scientific congresses.
Maintain and stay current on developments in atopic dermatitis and prurigo nodularis by review and study of relevant scientific literature.
Develop and conduct external and internal trainings and continuing education. (Examples include but not limited to – sales training, speaker training and advisory board alignment with HCPs).
Ensure all activities and responses with external and internal stakeholders are conducted timely and with strict adherence to legal and compliance guidelines.
Provide medical and scientific support into the planning and execution of advisory boards and work with physician experts to review speaker presentations and provide additional medical background where requested.

Benefits

You will be working for an organization that embraces diversity & inclusion and believe we will deliver better outcomes by reflecting the perspectives of our diverse customer base.
You will also have access to a range of company benefits, including a competitive wage with shift differential, annual bonus opportunities and career advancement and cross-training.

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