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Associate Director Biopharma Pharmaceutical Jobs

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How much do associate director biopharma pharmaceutical jobs pay per year?

As of Aug 8, 2026, the average yearly pay for associate director biopharma pharmaceutical in the United States is $102,728.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $141,000.00 per year, depending on experience, location, and employer.

What are the main challenges faced by an associate director in biopharma pharmaceutical, and how can candidates prepare to address them?

An Associate Director in Biopharma Pharmaceutical often navigates challenges such as managing cross-functional teams, ensuring regulatory compliance, and driving projects to meet tight deadlines. The role requires balancing strategic leadership with hands-on problem solving, as well as effective communication across departments like R&D, regulatory affairs, and commercial operations. Candidates can prepare by honing project management skills, staying updated on regulatory trends, and building experience in leading diverse scientific teams. Demonstrating adaptability and a proactive approach to stakeholder engagement will also be key to success.

What are the key skills and qualifications needed to thrive as an associate director in biopharma pharmaceutical, and why are they important?

To thrive as an Associate Director in Biopharma Pharmaceutical, you generally need a strong background in life sciences, advanced degrees (such as a PhD or PharmD), and extensive experience in drug development or pharmaceutical management. Expertise with regulatory systems (like FDA or EMA guidelines), clinical trial management software, and data analysis tools is commonly required. Leadership, strategic thinking, and excellent communication skills distinguish successful professionals in this role. These skills and qualities are crucial to drive innovation, ensure compliance, and effectively lead multidisciplinary teams in a highly regulated, competitive industry.

What does an associate director in biopharma pharmaceutical do?

An Associate Director in Biopharma Pharmaceutical oversees various aspects of drug development, regulatory compliance, and project management within a pharmaceutical company. They typically lead cross-functional teams, manage timelines and budgets, and ensure that projects align with both scientific standards and business goals. This role often involves collaborating with research, clinical, and commercial teams, as well as ensuring adherence to industry regulations. Associate Directors also contribute to strategic planning and mentor junior staff members.

What is the difference between Associate Director Biopharma Pharmaceutical vs Senior Scientist Biopharma Pharmaceutical?

AspectAssociate Director Biopharma PharmaceuticalSenior Scientist Biopharma Pharmaceutical
CredentialsAdvanced degree (PhD, MS) often required; leadership experience preferredTypically PhD or MS; strong research background
Work EnvironmentLeads teams, manages projects, interacts with cross-functional departmentsFocuses on research, experimental design, data analysis
Employer & Industry UsageUsed in biotech and pharma companies for managerial rolesCommon in R&D departments for scientific roles
Comparison Search IntentUnderstanding leadership and managerial responsibilitiesFocus on scientific expertise and research contributions

The Associate Director in Biopharma Pharmaceutical typically holds a leadership role, overseeing teams and projects, while the Senior Scientist focuses on scientific research and experimental work. Both roles require advanced degrees, but the Associate Director emphasizes management and strategic planning, whereas the Senior Scientist concentrates on scientific innovation and data analysis.

More about Associate Director Biopharma Pharmaceutical jobs
What cities are hiring for Associate Director Biopharma Pharmaceutical jobs? Cities with the most Associate Director Biopharma Pharmaceutical job openings:
What states have the most Associate Director Biopharma Pharmaceutical jobs? States with the most job openings for Associate Director Biopharma Pharmaceutical jobs include:
What job categories do people searching Associate Director Biopharma Pharmaceutical jobs look for? The top searched job categories for Associate Director Biopharma Pharmaceutical jobs are:
Infographic showing various Associate Director Biopharma Pharmaceutical job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $102,728 per year, or $49.4 per hour.

Associate Director / Director, US Policy and Patient Advocacy

Hansa Biopharma

Manhattan, NY • On-site

Full-time

Dental, Vision, Life, Retirement

Re-posted 23 days ago


Job description

About us
Hansa Biopharma is a fast-growing, commercial-stage biopharmaceutical company, pioneering the development and commercialization of innovative, lifesaving and life altering treatments for patients with acute or complex immune disorders.
Our broad therapeutic pipeline based on the company's proprietary IgG-cleaving enzyme technology platform has potential to address serious unmet medical needs in autoimmune diseases, gene therapy, and transplantation.
By empowering our people we move our projects forward with high speed, efficiency and scientific excellence. We strive to attract leading talent from around the world, broaden our network of partners and establish a presence in key markets around the world. There are many opportunities for highly qualified, motivated, and passionate team players to join us on our exciting journey.
Hansa Biopharma was founded in 2007, with the corporate headquarters in Lund, Sweden and has operations in other European countries and in the US. The Company has been listed on the Nasdaq First North Growth Market Stockholm from 2007 to 2015 and on the Nasdaq Stockholm since 2015.
Position summary : Associate Director / Director, US Policy and Patient Advocacy
Associate Director/Director of US Policy and Patient Advocacy play a pivotal role on the Global Corporate Affairs team at Hansa set and deliver the company's US policy and patient advocacy engagement strategy aligned with our corporate objectives and in rare immunological diseases business.
As part of the Global Corporate Affairs team, this role is responsible for analyzing the US policy and healthcare environment to identify opportunities and challenges impacting Hansa. The position develops and drives an actionable policy strategy, working closely with US Market Access and cross‑functional teams to support sustainable patient access to innovative therapies in rare disease.
The role leads engagement with Patient Advocacy Groups (PAGs) relevant to Hansa's therapeutic areas, building trusted relationships and structured collaboration plans. Through policy and patient advocacy initiatives, the role supports patient access, engagement, and collaboration across relevant parts of the healthcare ecosystem.
The role will serve as a bridge between patient organizations, and Hansa, working closely with US Patient Marketing, and ensuring that patient perspectives are reflected in relevant decision-making.
The individual in this role will report to the VP, Corporate Affairs.
This position will be hybrid and based in Hansa's NYC office and requires regular on-site presence, once the NYC office (Manhattan) is established.
Key tasks and responsibilities
This job description outlines key responsibilities but does not include all potential tasks or duties.
  • Analyze the US healthcare policy and external environment to identify opportunities and risks impacting Hansa's commercial and clinical‑stage programs.
  • Develop and execute a US policy and environment‑shaping plan to support commercialization planning and product launches in the US by ensuring policy and patient advocacy considerations are integrated early and effectively.
  • Collaborate closely with cross‑functional teams (Global Corporate Affairs, Market Access, Commercial, Medical Affairs, R&D) to deliver on agreed policy and patient advocacy priorities.
  • Build and maintain strategic relationships with policy makers, public health decisionmakers, and patient advocacy groups to advance Hansa's policy and patient engagement agenda.
  • Strategically identify and engage key Patient Advocacy Groups at US, national, and state levels, defining priority programs and partnership opportunities aligned with therapeutic areas.
  • Act as a trusted collaboration partner to Patient Advocacy Groups, supporting patient access, engagement, and education initiatives where appropriate and compliant.
  • Clearly and impactfully communicate Hansa's policy positions to external policy, public health, and patient advocacy stakeholders.
  • Bring the patients/patient organization perspective into relevant Hansa decision making process
  • Oversee and track corporate giving and PAG support initiatives, ensuring approved alignment with internal governance, compliance requirements, and ways of working.
  • Serve as an active and engaged member of the Global Corporate Affairs team, contributing to strategic development and cross‑enterprise collaboration.

Education and experience requirements
  • Bachelor's degree (BS/BA) in life sciences, public policy, business, or a related field required; advanced degree (e.g., MBA, MPH, or equivalent) preferred
  • Minimum of 5+ years of experience in patient advocacy and/or public policy within the pharmaceutical or biotechnology industry
  • Proven track record of developing and executing strategic initiatives/projects, including budget planning and management
  • Strong understanding of U.S. healthcare policy, regulatory frameworks, and compliance requirements related to patient advocacy engagement, with a demonstrated commitment to operating to the highest ethical standards
  • Experience of U.S. product launches is preferred
  • Therapeutic area experience in transplantation, rare diseases, and/or nephrology is strongly preferred

Capabilities and skills
  • Demonstrated excellent communication and interpersonal skills, with the ability to effectively engage and build relationships with patient advocacy organizations, policymakers, healthcare stakeholders, and internal cross-functional teams. Proven ability to deliver results in a structured, efficient, and high-quality manner
  • Strong stakeholder management skills, with the ability to influence and collaborate across diverse external and internal audiences
  • Demonstrated ability to lead initiatives, work collaboratively as part of a team, and contribute to a high-performing environment
  • High level of integrity, professionalism, and accountability
  • Willingness and ability to travel approximately 25%

Our culture and values
Working at Hansa is more than a job for us, and our culture is characterised by pride - pride in what we do, in our company, and in what we have achieved and will accomplish for patients around the world.
Our culture is built on our core values: Accountability, Courage, Integrity, and Pioneering. These values guide how we work, collaborate, and make decisions every day.
We know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the countries and communities in which we operate and ultimately the patients we exist to serve.
Reasons to join the Hansa Team
  • A position in a company that envisions life changing outcomes for patients with acute or serious immune mediated conditions.
  • The chance to be part of an innovative R&D-driven organisation with a strong desire to make a difference for people.
  • An opportunity to build a fully integrated biopharmaceutical company with global outreach.
  • An open-minded and welcoming atmosphere. Friendly, motivated and skilled colleagues with whom you can both laugh and work.

Hansa is an equal opportunity employer that values diversity. We provide equal opportunities to all employees and applicants for employment and prohibit discrimination or harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, marital status or any other characteristic protected by federal, state or local laws.
Estimated salary range for this role is $185,000 - $250,000 annually. The actual base salary offered may depend on a variety of factors, including the qualifications, skills and experience of the individual applicant, level of education attained, certifications or other professional licenses held, and the geographic location of the individual.The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.
U.S. based employees may be eligible for short-term and/ or long-term incentives, as well as participation in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, company holidays and well-being benefits.
Location
On-site/Hybrid position: NYC office
The process
All applicants should apply on Hansa Biopharma's website to be considered for employment. We do not accept unsolicited candidate introductions or referrals from third party recruiters and staffing agencies, and we are not responsible for any fees associated with unsolicited referrals.
Attach your CV in English only. Unfortunately, we are unable to review applications made in other languages.
The process is ongoing and we will review applications as they are received.
We look forward to receiving your application - join us and make significant contributions to Hansa Biopharma's research!
Please note: No external recruitment support is required. Only applications received directly will be considered.
Department G&A - 11000 - Corporate Affairs Locations New York Remote status Hybrid