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Associate Director Biopharma Pharmaceutical Jobs

Director, Biopharma & Consortia Engagement The Director, Biopharma & Consortia Engagement serves as ... Technical: Strong understanding of the oncology landscape, pharmaceutical partner needs ...

Director, Biopharma & Consortia Engagement The Director, Biopharma & Consortia Engagement serves as ... Technical: • Strong understanding of the oncology landscape, pharmaceutical partner needs ...

Job summary BostonGene is seeking a highly motivated Director, Biopharma Sales to drive growth across pharmaceutical and biotechnology organizations in North America. The ideal candidate combines ...

NY · On-site

$197.40 - $246.80/hr

Sumitomo Pharma Co., Ltd. (Sumitomo Pharma America, Inc.) is a global pharmaceutical company ... Job Overview The Director of New Product Planning (Biopharma) reports to the Executive Director, R& ...

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Associate Director Biopharma Pharmaceutical information

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$30.5K

$102.7K

$173K

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

As of Jul 31, 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 July 2026, with employment types broken down into 100% Full Time. Highlights an 80% In-person, and 20% Remote job distribution, with an average salary of $102,728 per year, or $49.4 per hour.

Director, Biopharma & Consortia Engagement

Natera

OR • On-site, Remote

Other

Re-posted 23 days ago


Natera rating

7.6

Company rating: 7.6 out of 10

Based on 37 frontline employees who took The Breakroom Quiz

60th of 120 rated laboratories


Job description

Director, Biopharma & Consortia Engagement

The Director, Biopharma & Consortia Engagement serves as the engagement lead for Natera's Biopharma Marketing organization, translating oncology business development priorities into external-facing programs that strengthen partner relationships and accelerate opportunity creation. This role owns the strategy and execution of congress presence, executive and educational events, KOL and consortia engagement plans, and other targeted programs for pharmaceutical companies, cooperative groups, and key external stakeholders. 

The position partners closely with BioPharma Business Development, Medical Affairs, Product, Commercial Marketing, and the Event Marketing team to ensure engagement activities are insight-led, compliant, and measurable. This is a senior individual contributor role requiring strong oncology fluency, external stakeholder management, and the ability to lead complex programs in a highly matrixed environment.

PRIMARY RESPONSIBILITIES:

Develop and lead the annual biopharma engagement plan, including congress strategy, sponsored symposia, roundtables, executive events, roadshows, and other high-value touchpoints aligned to business development priorities.

Build and maintain KOL, consortia, and account influence maps; identify target stakeholders and define tailored engagement objectives, messaging, follow-up actions, and success metrics for priority programs.

Serve as the primary marketing interface to the Events function and coordinate with Business Development, Medical Affairs, Product, and Commercial Marketing teams to deliver high-quality, compliant external programs and partner-facing content.

Translate scientific data, publications, posters, and market insights into compelling narratives, event materials, and enablement assets that support partner conversations and account progression.

Gather and synthesize feedback from congresses, advisory boards, customer meetings, and consortia interactions to inform account strategy, campaign briefs, future event investments, and cross-functional decision-making.

Manage external agencies, vendors, budgets, timelines, and post-event reporting; monitor KPIs such as meeting volume, stakeholder engagement, pipeline influence, and return on program investment.

Performs other duties as assigned.

QUALIFICATIONS:

Bachelor's degree in life sciences, marketing, business, or a related discipline required; advanced degree (MBA, MS, PhD, or PharmD) preferred.

8+ years of progressively responsible experience in biotech, diagnostics, or pharmaceutical marketing, market development, partnerships, KOL engagement, or related commercial roles

Strong oncology experience required; experience in molecular diagnostics, genomics, MRD/ctDNA, precision medicine, or biopharma services strongly preferred.

Demonstrated success leading congress strategy, executive events, advisory boards, KOL engagement programs, or other external stakeholder initiatives in a regulated healthcare environment.

Experience translating complex scientific or clinical content into differentiated B2B messages, event programming, and commercial materials.

Proven ability to work cross-functionally with business development, medical affairs, product/clinical teams, legal/compliance, and external vendors.

Experience with account-based marketing, performance measurement, and program ROI tracking preferred.

Equivalent combination of education and relevant experience may be considered.

KNOWLEDGE, SKILLS, AND ABILITIES:

Technical:

Strong understanding of the oncology landscape, pharmaceutical partner needs, cooperative groups/consortia, and major congress/event ecosystems.

Ability to design engagement strategies, influence maps, stakeholder segmentation, target lists, and follow-up workflows tied to business goals.

Skilled in developing executive presentations, messaging frameworks, briefs, and sales/partner enablement materials from scientific content.

Working knowledge of CRM/lead capture processes, campaign analytics, event measurement, and reporting.

Strong project management, budget administration, vendor management, and compliant review/approval practices.

Behavioral:

Executive presence and strong interpersonal skills with the ability to represent the company credibly to senior external stakeholders.

Strategic, proactive, and solutions-oriented mindset with sound judgment and comfort operating in ambiguity.

Ability to lead without direct authority and align diverse cross-functional partners around shared priorities.

Strong written, verbal, and presentation skills; able to communicate complex information clearly and persuasively.

Highly organized, adaptable, and resilient, with the ability to manage multiple projects and deadlines simultaneously.

PHYSICAL DEMANDS & WORK ENVIRONMENT:

Work is primarily performed in an office, home office, or conference setting and requires regular use of a computer, keyboard, and standard office technology. The position requires the ability to review written materials, prepare presentations, and communicate effectively with internal and external stakeholders by phone, video conference, and in person. Periodic travel is required for congresses, customer meetings, advisory boards, and internal planning meetings, which may include evening or weekend hours. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions of the role.


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