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Biotech Director Jobs in Virginia (NOW HIRING)

American National Red Cross

Medical Director

Richmond, VA · On-site

$200K - $250K/yr

Direct medical strategy and operations for regulated cellular therapies (HPCs, CAR-T, Leukopaks ... Act as the primary medical liaison for biotech partners, providing expert guidance on donor ...

American National Red Cross

Medical Director

Roanoke, VA · On-site

$200K - $250K/yr

Direct medical strategy and operations for regulated cellular therapies (HPCs, CAR-T, Leukopaks ... Act as the primary medical liaison for biotech partners, providing expert guidance on donor ...

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All JobsBiotech JobsBiotech Director JobsBiotech Director Jobs in Virginia

Biotech Director information

See Virginia salary details

$24.8K

$94.6K

$185.3K

How much do biotech director jobs pay per year?

As of Aug 2, 2026, the average yearly pay for biotech director in Virginia is $94,626.00, according to ZipRecruiter salary data. Most workers in this role earn between $57,379.00 and $120,593.00 per year, depending on experience, location, and employer.

What are some common challenges faced by Biotech Directors and how are they addressed?

Biotech Directors often encounter challenges such as balancing regulatory compliance with innovation, managing cross-functional teams, and adapting to fast-paced advancements in technology. Addressing these issues requires staying informed on industry regulations, fostering a culture of open communication, and implementing effective project management strategies. Directors typically work closely with scientists, regulatory specialists, and business development teams to align project timelines, budgets, and objectives. Overcoming these challenges is a rewarding aspect of the role and helps drive organizational success in a competitive industry.

What are the key skills and qualifications needed to thrive in the Biotech Director position, and why are they important?

To thrive as a Biotech Director, you need advanced expertise in biotechnology, project management, and leadership, usually demonstrated by a relevant advanced degree and substantial industry experience. Familiarity with laboratory information management systems (LIMS), regulatory compliance protocols (such as FDA or EMA), and certifications like PMP or Six Sigma are highly valued. Excellent communication, problem-solving, and team-building skills help Biotech Directors effectively coordinate multidisciplinary teams and drive innovation. These skills and qualities ensure projects are completed efficiently, regulatory standards are met, and company goals in research and product development are achieved.

What does a Biotech Director do?

A Biotech Director oversees research, development, and operational strategies in a biotechnology company or department. They manage teams, ensure regulatory compliance, and drive innovation to develop new products or therapies. Responsibilities often include budgeting, partnerships, and aligning company goals with scientific advancements. Strong leadership, technical expertise, and industry knowledge are essential for success in this role.

What are the most commonly searched types of Biotech jobs in Virginia? The most popular types of Biotech jobs in Virginia are:
What are popular job titles related to Biotech Director jobs in Virginia? For Biotech Director jobs in Virginia, the most frequently searched job titles are:
What job categories do people searching Biotech Director jobs in Virginia look for? The top searched job categories for Biotech Director jobs in Virginia are:
What cities in Virginia are hiring for Biotech Director jobs? Cities in Virginia with the most Biotech Director job openings:
Biotech Director jobs near you
Infographic showing various Biotech Director job openings in Virginia as of July 2026, with employment types broken down into 94% Full Time, and 6% Contract. Highlights an 85% In-person, 3% Hybrid, and 12% Remote job distribution, with an average salary of $94,626 per year, or $45.5 per hour.

Associate Director, Research - European Pharmaceuticals and Biotechnology Regulation

Politico

Arlington, VA • On-site

Full-time

Re-posted 28 days ago

Job description

Job Description:
POLITICO is seeking an Associate Director, Research to help lead part of its regulatory intelligence and information services product, AgencyIQ. Since its founding in early 2020, AgencyIQ has quickly become the premier source of regulatory intelligence and analysis for professionals working in the life sciences, foods and chemicals industries.
Our written research and analysis is relied upon by many top companies, trade groups, law firms and advocacy groups to help them understand breaking news, identify emerging trends, predict future action and prepare for seismic shifts in regulatory policy.
As a subject matter expert in the regulation of pharmaceuticals, biopharmaceuticals and biotech in Europe - by the European Medicines Agency and other European regulatory authorities - the Associate Director will be responsible for analyzing the relevance of regulatory changes and developments, articulating the type and degree of impact on industry, and providing context to an audience of knowledgeable regulatory professionals.
We're looking for a regulatory expert who is as knowledgeable about regulatory topics as they are capable of explaining complex subjects to others quickly and effectively.
Reporting to the Senior Director for Life Sciences Research, the Associate Director will join a team of experienced researchers responsible for producing a mix of daily written content, in-depth written research, weekly insights, directed deliverables and presentations.
This role can be based at POLITICO's headquarters in Arlington, Virginia or at POLITICO's European offices in London or Brussels.
What You'll Do
  • Produce daily (3-4 per week) topical intelligence articles and other content for our subscribers based on emerging regulatory and legislative developments and trends

  • Serve as a subject matter specialist on matters of related to how European life sciences regulatory agencies regulate pharmaceuticals, biopharmaceuticals, biotechnology products, biosimilars, generic drugs, and nonprescription products

  • Lead or participate in the development and delivery of in-depth analysis, deep-dive research, webinars and email newsletters

  • Participate in subscriber- and prospect-facing events and regular briefings

What you'll need
  • At least 7 years' experience analyzing European life sciences regulatory policies at a consulting company, think tank, trade association, government agency, life sciences company, or media outlet

  • An affinity for writing - efficiently and effectively, and for a business or policy audience - paired with a knowledge of (and passion for) regulation and regulatory policy

  • Advanced-level (and preferably expert-level) knowledge of European regulatory processes related to drug and biotechnology products; capable of delivering expert insights to our knowledgeable subscribers

  • Experience and comfort working in fast-paced, research-driven environments in which daily delivery of written regulatory analyses of new information is the norm

  • Experience with qualitative and quantitative analysis and trend tracking

While not required, you will stand out if you:
  • Have an advanced degree or certification related to the life sciences (i.e., a PhD, relevant master's degree, or J.D.)

  • Have prior experience working in media, including as a journalist or writing a product widely read by others (i.e., a business intelligence product or internal newsletter)

  • Have experience in quantitative analysis using EMA data sets

  • Experience presenting on regulatory topics to a variety of different audience types (small groups, large groups) in different environments (virtual and in-person)

We value our people. Click here for more on what we offer and what it's like to work for POLITICO.
Let's keep in touch. You can view our list of open positions here.
About Us.
POLITICO illuminates the forces shaping global power. Since 2007, we have delivered intelligence that anticipates tomorrow's headlines, not reports on yesterday's news. As politics has increasingly become the defining force of our era, our work has never been more vital.
Cabinet secretaries and Ministers start their mornings with our analysis. CEOs shape strategy around our reporting. Advocacy leaders rely on our insights to move policy. We deliver the straightforward facts and clear-eyed analysis they need to navigate the most complex political landscape of our lifetimes.
Our 1,100+ publishing professionals across the world's key democratic capitals-Washington, Brussels, London, Paris, Berlin, Sacramento, and New York-form the world's premier politics and policy newsroom. We tell the story of how power really works by explaining who wields it and how they plan to exercise it, connecting dots others miss and delivering scoops from sources others don't even know exist.
Innovation has always been a core tenet of our story. At launch, we bet that depth would trump scale, that talent would trump traffic, and that politics would become central to modern life. In 2011, we made another bet and launched POLITICO Pro to help decision-makers understand the business of government, transforming both how they shape government action and the business of journalism itself.
These bets have made POLITICO the most successful digital news startup of its generation and the indispensable resource for leaders who shape the future. Today, we are a rarity in media: a growing, profitable, and sustainable news organization.
POLITICO is a subsidiary of Axel Springer SE, a family-owned transatlantic media company headquartered in Berlin and New York. Axel Springer is dedicated to shaping the future of journalism in the free world, believing that a free and informed society is essential to democracy. The company's guiding principles - first articulated as The Essentials by founder Axel Springer in the aftermath of World War II - remain a cornerstone of the company's foundation today. Learn more about Axel Springer
Posting date:
2026-04-07
Title:
Associate Director, Research - European Pharmaceuticals and Biotechnology Regulation

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