Acadia Pharmaceuticals Inc.
Medical Science Liaison Long-Term Care- New England
Acadia Pharmaceuticals Inc., Montgomery, Alabama, United States
Overview
About Acadia Pharmaceuticals Acadia is advancing breakthroughs in neuroscience to elevate life. Since our founding, we have been working at the forefront of healthcare to bring vital solutions to people who need them most. We developed and commercialized the first and only FDA-approved drug to treat hallucinations and delusions associated with Parkinson's disease psychosis, and the first and only approved drug in the United States and Canada for the treatment of Rett syndrome. Our clinical-stage development efforts are focused on Prader-Willi syndrome, Alzheimer's disease psychosis, and multiple other programs targeting neuro-psychiatric and neuro-rare diseases. For more information, visit Acadia.com and follow us on LinkedIn and X. Seeking talent near: Bridgeport, CT; Portland, ME; Boston, MA; New York, NY; Newark, NJ or Philadelphia, PA
Position Summary
Responsible for supporting medical and scientific initiatives on behalf of the Company's selected therapeutic areas. Develops ongoing professional relationships with national/regional healthcare Long-Term Care (LTC) practitioners and facilitates the education of these practitioners and their colleagues regarding current and forthcoming therapies developed and commercialized by the Company. Ensures access to current medical and scientific information on Company products and areas of therapeutic interest to targeted key opinion leaders (KOLs), healthcare professionals (HCPs), Managed Market and Long-Term Care (LTC) stakeholders and decision makers consistent with the objectives of Acadia and the Medical Affairs Department. This position is geographically based.
Primary Responsibilities
Identifies and develops relationships with national and regional medical and scientific LTC thought leaders, decision makers, medical and nursing directors, consistent with the strategy and objectives of Acadia's Medical Affairs Department. Engages LTC national and regional thought leaders to align interests, discuss research and medical information, and participate in scientific exchange and education about current and emerging therapies. Provides appropriate research trial support and investigator-initiated research proposal facilitation in the LTC setting. Develops and maintains scientific knowledge for company approved product(s). Identifies disease concepts and compound characteristics that can be leveraged into product differentiation. Provides appropriate scientific, clinical, and educational support for internal and external clients. Represents the company at specific continuing educational events, programs, medical meetings and conventions. Supports commercial operations by participating in Speaker and Sales Training. Partners with the internal departments to ensure accurate delivery of medical and scientific information. Cross-functionally collaborates, following all compliance guidelines, with regional field leadership partners including HEOR Field Directors, Long-term Care RAMs and regional field managers (RSMs) and Account Managers (AMs). Provides field strategic insights. Collaborates with medical affairs, clinical and commercial leadership to develop LTC strategies and field initiatives for the company and MSL team. Works closely with therapeutic MSLs to help coordinate LTC engagement in the region. Performs other duties as assigned.
Education/Experience/Skills
PharmD, PhD, MD/DO, DNP in a related field required. Targeting 5 years of progressively responsible experience in the biopharmaceutical industry and/or LTC setting. Previous MSL experience desired. Psychiatry or neurology experience strongly preferred. An equivalent combination of relevant education and experience may be considered. Key Skills: Expert scientific and pharmaceutical knowledge applied to the LTC setting. Knowledge of regulatory, compliance, commercial, and clinical issues affecting the pharmaceutical and managed care industries in the LTC segment. Knowledge of LTC customer segments and market dynamics. Skilled as a poised and knowledgeable presenter of scientific information, including excellent writing capabilities and strong demonstrated presentation skills for external formats such as physician gatherings and medical congresses. Experience in preparation of materials for use by Medical Affairs, including reviewing/editing Promotional materials. Excellent planning and organizational skills. Ability to professionally collaborate and interact with all levels within the organization. Skilled at negotiating with business partners or management and influencing leaders. Ability to work independently and with cross-functional teams. Ability to take initiative and demonstrate follow-through skills. Excellent oral and written communication skills. Demonstrated expertise in drug information communication. Highly skilled with MS Office programs (Outlook, Word, Excel, PowerPoint). Ability to travel up to 75% of time, with primary residence within the geographical area.
Physical Requirements
This role involves regular standing, walking, sitting, and the use of hands for handling or operating equipment. The employee may also need to reach, climb, balance, stoop, kneel, crouch, and maintain visual, verbal, and auditory communication in a standard office environment and while working independently from remote locations. The employee must occasionally lift and/or move up to 20 pounds. This position requires the ability to travel independently overnight and/or work after hours as required by travel schedules or business needs.
#LI-REMOTE #elev8
In addition to a competitive base salary, this position is also eligible for discretionary bonus and equity awards based on factors such as individual and organizational performance. Actual amounts will vary depending on experience, performance, and location.
Salary Range $139,600 — $174,500 USD
What we offer US-based Employees
Competitive base, bonus, new hire and ongoing equity packages Medical, dental, and vision insurance Employer-paid life, disability, business travel and EAP coverage 401(k) Plan with a fully vested company match 1:1 up to 5% Employee Stock Purchase Plan with a 2-year purchase price lock-in 15+ vacation days 13 -15 paid holidays, including office closure between December 24th and January 1st 10 days of paid sick time Paid parental leave benefit Tuition assistance
EEO Statement (US-based Employees):
Acadia is committed to building a diverse, equitable, inclusive, and innovative company. We are an equal opportunity employer and encourage candidates from all backgrounds to apply.
As an equal opportunity employer, Acadia is committed to a diverse workforce. If you are a qualified individual with a disability or a disabled veteran, you have the right to request a reasonable accommodation. To request accommodations, please contact talentacquisition@acadia-pharm.com or 858-261-2923.
Please note that reasonable accommodations granted throughout the recruiting process are not guaranteed to be the same accommodations given if hired. A new request will need to be submitted for any ADA accommodations after starting employment.
California Applicants:
See Additional Information for California Residents within our Privacy Policy.
Canadian Applicants:
See Additional Information for Canadian Residents within our Privacy Policy.
Applicants in the European Economic Area, Switzerland, the United Kingdom, and Serbia:
See Additional Information for Individuals in the European Economic Area, Switzerland, the United Kingdom, and Serbia within our Privacy Policy.
Notice to Search Firms/Third-Party Recruitment Agencies (Recruiters):
The Talent Acquisition team manages the recruitment and employment process for Acadia. We do not accept resumes from recruiters or search firms without an executed search agreement in place. Resumes sent to Acadia employees in the absence of an agreement will not obligate Acadia in any way.
#J-18808-Ljbffr
About Acadia Pharmaceuticals Acadia is advancing breakthroughs in neuroscience to elevate life. Since our founding, we have been working at the forefront of healthcare to bring vital solutions to people who need them most. We developed and commercialized the first and only FDA-approved drug to treat hallucinations and delusions associated with Parkinson's disease psychosis, and the first and only approved drug in the United States and Canada for the treatment of Rett syndrome. Our clinical-stage development efforts are focused on Prader-Willi syndrome, Alzheimer's disease psychosis, and multiple other programs targeting neuro-psychiatric and neuro-rare diseases. For more information, visit Acadia.com and follow us on LinkedIn and X. Seeking talent near: Bridgeport, CT; Portland, ME; Boston, MA; New York, NY; Newark, NJ or Philadelphia, PA
Position Summary
Responsible for supporting medical and scientific initiatives on behalf of the Company's selected therapeutic areas. Develops ongoing professional relationships with national/regional healthcare Long-Term Care (LTC) practitioners and facilitates the education of these practitioners and their colleagues regarding current and forthcoming therapies developed and commercialized by the Company. Ensures access to current medical and scientific information on Company products and areas of therapeutic interest to targeted key opinion leaders (KOLs), healthcare professionals (HCPs), Managed Market and Long-Term Care (LTC) stakeholders and decision makers consistent with the objectives of Acadia and the Medical Affairs Department. This position is geographically based.
Primary Responsibilities
Identifies and develops relationships with national and regional medical and scientific LTC thought leaders, decision makers, medical and nursing directors, consistent with the strategy and objectives of Acadia's Medical Affairs Department. Engages LTC national and regional thought leaders to align interests, discuss research and medical information, and participate in scientific exchange and education about current and emerging therapies. Provides appropriate research trial support and investigator-initiated research proposal facilitation in the LTC setting. Develops and maintains scientific knowledge for company approved product(s). Identifies disease concepts and compound characteristics that can be leveraged into product differentiation. Provides appropriate scientific, clinical, and educational support for internal and external clients. Represents the company at specific continuing educational events, programs, medical meetings and conventions. Supports commercial operations by participating in Speaker and Sales Training. Partners with the internal departments to ensure accurate delivery of medical and scientific information. Cross-functionally collaborates, following all compliance guidelines, with regional field leadership partners including HEOR Field Directors, Long-term Care RAMs and regional field managers (RSMs) and Account Managers (AMs). Provides field strategic insights. Collaborates with medical affairs, clinical and commercial leadership to develop LTC strategies and field initiatives for the company and MSL team. Works closely with therapeutic MSLs to help coordinate LTC engagement in the region. Performs other duties as assigned.
Education/Experience/Skills
PharmD, PhD, MD/DO, DNP in a related field required. Targeting 5 years of progressively responsible experience in the biopharmaceutical industry and/or LTC setting. Previous MSL experience desired. Psychiatry or neurology experience strongly preferred. An equivalent combination of relevant education and experience may be considered. Key Skills: Expert scientific and pharmaceutical knowledge applied to the LTC setting. Knowledge of regulatory, compliance, commercial, and clinical issues affecting the pharmaceutical and managed care industries in the LTC segment. Knowledge of LTC customer segments and market dynamics. Skilled as a poised and knowledgeable presenter of scientific information, including excellent writing capabilities and strong demonstrated presentation skills for external formats such as physician gatherings and medical congresses. Experience in preparation of materials for use by Medical Affairs, including reviewing/editing Promotional materials. Excellent planning and organizational skills. Ability to professionally collaborate and interact with all levels within the organization. Skilled at negotiating with business partners or management and influencing leaders. Ability to work independently and with cross-functional teams. Ability to take initiative and demonstrate follow-through skills. Excellent oral and written communication skills. Demonstrated expertise in drug information communication. Highly skilled with MS Office programs (Outlook, Word, Excel, PowerPoint). Ability to travel up to 75% of time, with primary residence within the geographical area.
Physical Requirements
This role involves regular standing, walking, sitting, and the use of hands for handling or operating equipment. The employee may also need to reach, climb, balance, stoop, kneel, crouch, and maintain visual, verbal, and auditory communication in a standard office environment and while working independently from remote locations. The employee must occasionally lift and/or move up to 20 pounds. This position requires the ability to travel independently overnight and/or work after hours as required by travel schedules or business needs.
#LI-REMOTE #elev8
In addition to a competitive base salary, this position is also eligible for discretionary bonus and equity awards based on factors such as individual and organizational performance. Actual amounts will vary depending on experience, performance, and location.
Salary Range $139,600 — $174,500 USD
What we offer US-based Employees
Competitive base, bonus, new hire and ongoing equity packages Medical, dental, and vision insurance Employer-paid life, disability, business travel and EAP coverage 401(k) Plan with a fully vested company match 1:1 up to 5% Employee Stock Purchase Plan with a 2-year purchase price lock-in 15+ vacation days 13 -15 paid holidays, including office closure between December 24th and January 1st 10 days of paid sick time Paid parental leave benefit Tuition assistance
EEO Statement (US-based Employees):
Acadia is committed to building a diverse, equitable, inclusive, and innovative company. We are an equal opportunity employer and encourage candidates from all backgrounds to apply.
As an equal opportunity employer, Acadia is committed to a diverse workforce. If you are a qualified individual with a disability or a disabled veteran, you have the right to request a reasonable accommodation. To request accommodations, please contact talentacquisition@acadia-pharm.com or 858-261-2923.
Please note that reasonable accommodations granted throughout the recruiting process are not guaranteed to be the same accommodations given if hired. A new request will need to be submitted for any ADA accommodations after starting employment.
California Applicants:
See Additional Information for California Residents within our Privacy Policy.
Canadian Applicants:
See Additional Information for Canadian Residents within our Privacy Policy.
Applicants in the European Economic Area, Switzerland, the United Kingdom, and Serbia:
See Additional Information for Individuals in the European Economic Area, Switzerland, the United Kingdom, and Serbia within our Privacy Policy.
Notice to Search Firms/Third-Party Recruitment Agencies (Recruiters):
The Talent Acquisition team manages the recruitment and employment process for Acadia. We do not accept resumes from recruiters or search firms without an executed search agreement in place. Resumes sent to Acadia employees in the absence of an agreement will not obligate Acadia in any way.
#J-18808-Ljbffr