Medical Science Liaison- Great Lakes
Scholar Rock
1 month ago
Remote
United States
Medical Affairs
Summary of Position:
- Represent the real-time voice of KOL/HCP input related to product development opportunities and scientific exchange on pipeline and commercial products.
- Conduct clinical presentations to payer organizations.
Position Responsibilities:
- Become an SMA and apitegromab medical/clinical/scientific expert.
- Build and foster relationships with local, regional, and national KOLs and possibly payers.
- Deliver medical/clinical/scientific presentations to diverse external audiences.
- Support clinical development activities, investigator recruitment, and education.
- Develop and execute a Territory Management Plan (TMP) aligned with overall Medical Goals and Plan.
- Contribute to MSL metrics and qualitative/quantitative reports, and to MSL SOPs/Business Practices.
- Respond to unsolicited medical information requests from SRRK field teams.
- Compliantly partner with Sales and Market Access on regional engagement.
- Provide internal teams insights from discussions with HCPs.
- Co-create and deliver MSL training; support development of MSL materials.
- Contribute to Global and US Medical Plans for apitegromab in SMA.
- Participate in advisory meetings, speaker trainings, and similar activities.
- Coordinate and manage local/regional Investigator-Initiated Research (IIR), including milestones and objectives.
- Report on scientific sessions and conduct scientific exchange at congresses; respond/document unsolicited scientific information requests.
- Perform activities in accordance with applicable legal, regulatory, and corporate regulations and guidelines.
Candidate Requirements (Qualifications):
- MD, PharmD, or PhD preferred; advanced professional degree (e.g., NP, PT) may be considered with significant clinical neuromuscular disease experience.
- Neurology and/or rare disease experience with prior launch experience preferred.
- Demonstrated knowledge of regulatory, commercial, and clinical issues affecting the pharmaceutical industry.
- Excellent verbal/written communication, presentation, and interpersonal skills.
- Strategic planning, organizational, and project management abilities.
- Ability to collaborate across geographic areas and cross-functional teams.
- Experience in a “start-up” biopharma company desirable.
- High integrity; committed to ethics and scientific standards.
- Ability to work independently and engage in collaborative decision-making in a rapidly paced environment.
- Customer relationship management program experience a plus.
- Remote role requiring extensive overnight travel (>50%).
Compensation:
- $220,000 - $250,000 per year.
- Represent the real-time voice of KOL/HCP input related to product development opportunities and scientific exchange on pipeline and commercial products.
- Conduct clinical presentations to payer organizations.
Position Responsibilities:
- Become an SMA and apitegromab medical/clinical/scientific expert.
- Build and foster relationships with local, regional, and national KOLs and possibly payers.
- Deliver medical/clinical/scientific presentations to diverse external audiences.
- Support clinical development activities, investigator recruitment, and education.
- Develop and execute a Territory Management Plan (TMP) aligned with overall Medical Goals and Plan.
- Contribute to MSL metrics and qualitative/quantitative reports, and to MSL SOPs/Business Practices.
- Respond to unsolicited medical information requests from SRRK field teams.
- Compliantly partner with Sales and Market Access on regional engagement.
- Provide internal teams insights from discussions with HCPs.
- Co-create and deliver MSL training; support development of MSL materials.
- Contribute to Global and US Medical Plans for apitegromab in SMA.
- Participate in advisory meetings, speaker trainings, and similar activities.
- Coordinate and manage local/regional Investigator-Initiated Research (IIR), including milestones and objectives.
- Report on scientific sessions and conduct scientific exchange at congresses; respond/document unsolicited scientific information requests.
- Perform activities in accordance with applicable legal, regulatory, and corporate regulations and guidelines.
Candidate Requirements (Qualifications):
- MD, PharmD, or PhD preferred; advanced professional degree (e.g., NP, PT) may be considered with significant clinical neuromuscular disease experience.
- Neurology and/or rare disease experience with prior launch experience preferred.
- Demonstrated knowledge of regulatory, commercial, and clinical issues affecting the pharmaceutical industry.
- Excellent verbal/written communication, presentation, and interpersonal skills.
- Strategic planning, organizational, and project management abilities.
- Ability to collaborate across geographic areas and cross-functional teams.
- Experience in a “start-up” biopharma company desirable.
- High integrity; committed to ethics and scientific standards.
- Ability to work independently and engage in collaborative decision-making in a rapidly paced environment.
- Customer relationship management program experience a plus.
- Remote role requiring extensive overnight travel (>50%).
Compensation:
- $220,000 - $250,000 per year.