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Home Flexible Job Board Associate Director, Thought Leader Liaison, Neurology Rare Disease - Central/West Region

$169,222–253,000/yr 5d ago

Associate Director, Thought Leader Liaison, Neurology Rare Disease - Central/West Region

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Otsuka Pharmaceutical Co., Ltd.

US

Full-time Permanent Remote

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Summary

The Associate Director will lead regional thought leader engagement and market development strategies for neurology rare disease products. They will coordinate with cross-functional teams to address barriers in the patient pathway and execute non-sales educational initiatives.

Job Description

Position Overview

The Associate Director, Thought Leader Liaison (TLL), Neurology Rare Disease is a senior, field-based, externally facing, non-sales commercial role reporting to the Senior Director, Marketing and Thought Leader Liaison. The role combines scientific fluency, strategic thought-leader engagement and regional business planning. The TLL builds trusted relationships with national, regional and emerging thought leaders and with organizations that influence the patient pathway from diagnosis through treatment and support.

The role identifies and helps address recurring barriers to earlier recognition, specialist referral, genetic testing, genetic counseling and connection to treatment-capable centers. The TLL integrates appropriate aggregate field insights into regional business plans, thought-leader engagement strategies and practical actions for disease education, market development and launch readiness.

The TLL executes non-sales relationship, education, network and barrier-removal activities and supports the  Account Manager  account planning and operational execution. The Account Manager retains responsibility for account sales execution and performance.

The TLL and Medical Science Liaison (MSL) coordinate on shared thought leaders, scientific needs and joint engagements. The TLL focuses on disease education, referral pathways and market development, while the MSL leads scientific exchange and Medical follow-up. 

Prior to regulatory approval, the TLL operates through approved, nonpromotional disease-state education, thought-leader engagement and market-development activities.

Upon regulatory approval, this role is expected to assume promotional responsibilities consistent with the approved label and company policy, including identification, training support, and quality monitoring of national and regional promotional faculty and speaker programs; label-consistent diagnostic, referral, and care-pathway education; and launch feedback and content optimization. Program quality, reach, and compliance, not prescription volume, remain the measures of this work.

The Central/West region is the primary coverage area, but the TLL may lead selected national relationships or initiatives based on experience and business needs.

Key Responsibilities

Regional Strategy, Network Mapping and Engagement

·    Develop and execute a regional plan aligned with national strategy and launch priorities.

·    Map priority institutions, thought leaders, and referral relationships to clarify how diagnosis, testing, counseling, referral, and treatment connect across the region.

·    Use regional and account-level insights to prioritize engagement, identify cross-account barriers, and recommend and support actions that strengthen the Account Manager’s planning and operational execution.

·    Coordinate with MSLs on shared thought leaders, scientific needs and joint engagements. The TLL focuses on disease education, referral pathways and market development, while Medical Affairs retains responsibility for scientific exchange and Medical follow-up.

Thought Leader Engagement

·    Establish and maintain compliant relationships with national and regional experts, center leaders and influential community and neuromuscular practices. Develop engagement plans for priority thought leaders and institutions.

·    Develop and execute, in partnership with Marketing, approved national and regional peer-to-peer education programs that connect experts and centers with community professional networks and address identified educational and referral needs. Programs are disease-state and nonpromotional prior to regulatory approval, and branded, label-consistent and promotional following approval.

·    Identify qualified advisors and, following approval, promotional faculty based on documented business need, objective criteria and approved processes. Contracting and compensation decisions remain with designated company functions.

Insight Generation and Strategic Translation

·    Capture and synthesize aggregate, non-patient-specific insights from field engagements, including recurring patterns in disease recognition, genetic testing and counseling, referral, treatment readiness and support.

·    Compare insights across accounts to distinguish isolated account issues from broader regional barriers. Incorporate findings into regional business plans, recommend appropriate action and support implementation within the TLL’s responsibilities.

·    Maintain knowledge of the publicly available disease, treatment, evidence and competitive landscape. Share relevant implications with approved internal partners and refer scientific evidence needs to Medical Affairs or HEOR.

Regional Advocacy Engagement

·    Serve as the regional relationship lead for approved engagement with local and regional advocacy organizations under the strategy and governance of National Patient Advocacy.

·    Identify opportunities to use approved advocacy resources, programs and professional networks to address regional education, referral and support needs. Bring aggregate regional insights to National Patient Advocacy and other internal partners.

·    Provide regional input on potential partnerships and sponsorships. Approval, contracting, grants and funding decisions remain with the designated company functions.

Congress and Professional Meeting Leadership

·    Lead the commercial thought-leader engagement strategy for priority national and regional congresses and professional-society meetings, coordinating objectives and follow-up with Marketing, Medical Affairs and field partners.

·    Use congress engagement to strengthen relationships, identify emerging thought leaders and capture relevant field insights. Medical Affairs retains responsibility for scientific exchange and investigational product discussions.

Cross-Functional Collaboration

·    Partner with Marketing leadership to inform launch strategy, disease-education needs, peer-to-peer programs, congress planning and, following approval, faculty strategy.

·    Work with Account Manager and other functional partners to translate regional insights into coordinated action while preserving functional responsibilities.

·    Coordinate scientific needs with Medical Affairs, access needs with Market Access, patient support with Patient Services, and implementation with Account Manager or the appropriate owner. Report safety information and product complaints through required company processes.

Qualifications

·    Bachelor’s degree required; an advanced clinical, scientific, public health or business degree or relevant clinical credential is preferred.

·    At least eight years of relevant biopharmaceutical experience, including field marketing, TLL, market development, product marketing, thought-leader engagement or another strategic field role.

·    Recent experience in rare or ultra-rare disease, neurology, neuromuscular disease, genetics, or diagnostics strongly preferred.

·    Demonstrated pre-launch and launch experience, including the ability to operate within distinct pre- and post-approval engagement boundaries.

·    Demonstrated ability to operate independently and compliantly in a field role without an established franchise infrastructure.

·    Strong clinical and scientific fluency sufficient for credible disease-state discussions with senior specialist audiences.

Skills and Other Requirements

·    Leadership, strategic thinking, sound judgment, and the ability to translate ambiguity into an executable field plan.

·    Exceptional relationship-building skills and executive presence with senior clinicians, professional organizations, and cross-functional colleagues.

·    Disciplined judgment regarding commercial, medical role boundaries and pre- and post-approval engagement rules.

·    Strong analytical ability to map influence networks, diagnostic and referral workflows, and regional opportunities; ability to produce concise, actionable, aggregate insights.

·    Excellent written, verbal, facilitation, and presentation skills; experience with advisory boards, and with execution and quality oversight of disease state programs before approval and branded speaker program post approval.

·    Proficiency with CRM, insight-management, virtual engagement, and standard business platforms; commitment to documentation quality, privacy, and company policies.

Other Requirements

·    Field-based role; willingness and ability to travel more than 50% of the time, including significant overnight and occasional weekend travel.

·    Ability to attend priority national and regional congresses, advisory boards, and evening programs as business needs require.

·    Valid driver's license; ability to meet company fleet, driving, and travel requirements.

·    Assigned geography: Central/West region. Candidates must reside within the Central/West territory within practical reach of a major hub airport; residence in Chicago, Dallas or Denver cities preferred. Candidates outside the preferred cities will be considered if they can demonstrate efficient coverage of full territory.

Competencies
Accountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
Strategic Thinking & Problem Solving - Make decisions considering the long-term impact to customers, patients, employees, and the business.
Patient & Customer Centricity - Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
Impactful Communication - Communicate with logic, clarity, and respect. Influence at all levels to achieve the best results for Otsuka.
Respectful Collaboration - Seek and value others’ perspectives and strive for diverse partnerships to enhance work toward common goals.
Empowered Development - Play an active role in professional development as a business imperative.

Minimum $169,222.00 - Maximum $253,000.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate’s job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.

Application Deadline: This will be posted for a minimum of 5 business days.

Company benefits:  Comprehensive medical, dental, vision, prescription drug coverage, company provided basic life, accidental death & dismemberment, short-term and long-term disability insurance, tuition reimbursement, student loan assistance, a generous 401(k) match, flexible time off, paid holidays, and paid leave programs as well as other company provided benefits.

Come discover more about Otsuka and our benefit offerings; https://ah-prod.com/multi/videoplayer/player.html?v=6385356920112.

Join Our Talent Community: Stay connected with Otsuka by joining our Talent Community. Tell us about your interests, and we’ll notify you about future opportunities that align with your background. https://community.hireez.com/cielo-otsuka/82cb3591

Disclaimer: 

This job description is intended to describe the general nature and level of the work being performed by the people assigned to this position. It is not intended to include every job duty and responsibility specific to the position. Otsuka reserves the right to amend and change responsibilities to meet business and organizational needs as necessary. 

Otsuka is an equal opportunity employer.  All qualified applicants are encouraged to apply and will be given consideration for employment without regard to race, color, sex, gender identity or gender expression, sexual orientation, age, disability, religion, national origin, veteran status, marital status, or any other legally protected characteristic.   

If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation, if you are unable or limited in your ability to apply to this job opening as a result of your disability.  You can request reasonable accommodations by contacting [email protected]. 

Statement Regarding Job Recruiting Fraud Scams

At Otsuka we take security and protection of your personal information very seriously. Please be aware individuals may approach you and falsely present themselves as our employees or representatives.  They may use this false pretense to try to gain access to your personal information or acquire money from you by offering fictitious employment opportunities purportedly on our behalf.

Please understand, Otsuka will never ask for financial information of any kind or for payment of money during the job application process. We do not require any financial, credit card or bank account information and/or any payment of any kind to be considered for employment. We will also not offer you money to buy equipment, software, or for any other purpose during the job application process. If you are being asked to pay or offered money for equipment fees or some other application processing fee, even if claimed you will be reimbursed, this is not Otsuka. These claims are fraudulent and you are strongly advised to exercise caution when you receive such an offer of employment.

Otsuka will also never ask you to download a third-party application in order to communicate about a legitimate job opportunity. Scammers may also send offers or claims from a fake email address or from Yahoo, Gmail, Hotmail, etc, and not from an official Otsuka email address. Please take extra caution while examining such an email address, as the scammers may misspell an official Otsuka email address and use a slightly modified version duplicating letters.

To ensure that you are communicating about a legitimate job opportunity at Otsuka, please only deal directly with Otsuka through its official Otsuka Career website https://vhr-otsuka.wd1.myworkdayjobs.com/en-US/External.

Otsuka will not be held liable or responsible for any claims, losses, damages or expenses resulting from job recruiting scams. If you suspect a position is fraudulent, please contact Otsuka’s call center at: 800-363-5670. If you believe you are the victim of fraud resulting from a job recruiting scam, please contact the FBI through the Internet Crime Complaint Center at: https://www.ic3.gov,  or your local authorities.

Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and Otsuka Precision Health, Inc. (“Otsuka”) does not accept unsolicited assistance from search firms for employment opportunities.  All CVs/resumes submitted by search firms to any Otsuka employee directly or through Otsuka’s application portal without a valid written search agreement in place for the position will be considered Otsuka’s sole property.  No fee will be paid if a candidate is hired by Otsuka as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails. 

About the company

Otsuka Pharmaceutical Co., Ltd.

There are two Otsuka pharmaceutical industry companies in the U.S.:

Otsuka America Pharmaceutical, Inc. (OAPI) successfully commercializes Otsuka-discovered and in-licensed products in North America.

Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC) clinically develops and registers innovative healthcare products on a global basis.

Company size

1,001-5,000 employees

Industry

Pharmaceutical Manufacturing

Org type

Privately Held

Headquarters

Princeton, NJ

Apply Now

About the company

Otsuka Pharmaceutical Co., Ltd.

There are two Otsuka pharmaceutical industry companies in the U.S.:

Otsuka America Pharmaceutical, Inc. (OAPI) successfully commercializes Otsuka-discovered and in-licensed products in North America.

Otsuka Pharmaceutical Development & Commercialization, Inc. (OPDC) clinically develops and registers innovative healthcare products on a global basis.

Company size

1,001-5,000 employees

Industry

Pharmaceutical Manufacturing

Org type

Privately Held

Headquarters

Princeton, NJ

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