Medical Science Liaison

Posted Sep 5

This is a fully remote position, open to applicants in Oklahoma, +1 more state.

📋 Description

• Cultivate and sustain relationships with regional, national, and international key opinion leaders in the fields of Neurology, Adult Physical Rehabilitation Medicine, and ENT.

• Address and document unsolicited medical information inquiries from healthcare professionals and payers.

• Create and execute educational messaging strategies for Merz Therapeutics products.

• Oversee scientific exchanges and deliver balanced scientific responses to managed-care decision-makers.

• Support grants, investigator-initiated studies, advocacy/speaking engagements, and educational requests.

• Keep abreast of clinical knowledge regarding the Merz Therapeutics portfolio and its competitors.

• Provide competitive intelligence to internal teams.

• Organize and manage activities related to medical congresses, schedules, meetings, and key opinion leader interactions.

• Train congress faculty on the science behind the portfolio and identify educational opportunities.

• Attend pertinent medical meeting sessions, correct misinformation, and prepare post-meeting summaries.

• Act as the designated product lead expert for clinical and scientific commercial needs.

• Develop brand workshops, training sessions, medical affairs presentations, and scientific materials.

• Conduct scientific and clinical workshops for internal meetings.

• Facilitate investigator-initiated studies, including milestones, recruitment, enrollment, and publication planning.

• Provide insights from thought leaders and investigators to Medical/Clinical teams.

• Enable investigator interactions with R&D.

• Assist with Medical Affairs advisory boards to identify knowledge gaps, resolve issues, support product development, and foster treatment-guideline consensus.

• Travel throughout the designated Texas and Oklahoma territory for key opinion leader visits, managed markets meetings, and medical meetings.


⛳️ Requirements

• Must reside near a major airport within the Texas and Oklahoma territory.

• Possess an advanced degree (PharmD, PhD, or MD).

• Minimum of one year of experience as an MSL or in a related industry role.

• Adhere to corporate standard operating procedures and comply with legal and regulatory guidelines governing scientific interactions.

• Comply with relevant laws, regulations, and regulatory guidelines that oversee commercial and scientific interactions.

• Maintain adherence to company compliance policies and governmental regulations.

• Have a working knowledge of the PhRMA and AdvaMed Codes as well as FDA regulations concerning the marketing of prescription drugs and medical devices.

• Strong clinical knowledge in pertinent therapeutic areas.

• Business acumen and familiarity with the therapeutics/neurosciences industry and the medical device/pharmaceutical regulatory and compliance landscape.

• Proficient in Microsoft Word, Excel, and PowerPoint.

• Excellent interpersonal skills.

• Outstanding verbal and written communication abilities.

• Capability to clearly convey complex scientific concepts in both one-on-one and group settings.

• Strong multitasking, time management, and organizational capabilities.

• Willingness and ability to travel at least 60%, including potential weekends and overnight stays.


🏝️ Benefits

• An inclusive culture that fosters individual development and collaborative teamwork.

• Opportunities to contribute to the common good and grow together as a family.

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