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Project Manager Biotech Jobs in Kansas (NOW HIRING)

Amgen

$71K - $96K/yr

Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Actively participate in Capital Project Environmental assessments and design process. * Apply a ...

Clarivate Analytics

Manage project timelines, budgets, and resource allocation to ensure that customer objectives are ... biotechnology and MedTech companies. We combine deep domain expertise and data-driven analysis to ...

Clarivate

Manage project timelines, budgets, and resource allocation to ensure that customer objectives are ... biotechnology and MedTech companies. We combine deep domain expertise and data-driven analysis to ...

Clayco (LJC)

Lead Mechanical Engineer

Lenexa, KS · On-site

$102K - $124K/yr

... biotechnology production environments. This role focuses on air-side systems and building-side ... and manage multiple priorities. Some Things You Should Know * Our clients and projects are ...

Ceva Santé Animale

QA Validation Engineer

Lenexa, KS · On-site

... management pre-approval. Coordinate qualification execution and all aspects of validation projects ... Bachelor's degree in Engineering, Biotechnology, Biology, or Microbiology with 4+ years of ...

Clayco (LJC)

Lead Mechanical Engineer

Lenexa, KS · On-site

$102K - $124K/yr

... biotechnology production environments. This role focuses on air-side systems and building-side ... and manage multiple priorities. Some Things You Should Know * Our clients and projects are ...

Clayco (LJC)

Lead Mechanical Engineer

Lenexa, KS · On-site

$102K - $124K/yr

... biotechnology production environments. This role focuses on air-side systems and building-side ... and manage multiple priorities. Some Things You Should Know * Our clients and projects are ...

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Project Manager Biotech information

See Kansas salary details

$19

$41

$68

How much do project manager biotech jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for project manager biotech in Kansas is $41.24, according to ZipRecruiter salary data. Most workers in this role earn between $35.82 and $45.24 per hour, depending on experience, location, and employer.

What is the difference between Project Manager Biotech vs Clinical Project Manager?

AspectProject Manager BiotechClinical Project Manager
CredentialsBachelor's or Master's in Life Sciences, Project Management CertificationBachelor's or Master's in Life Sciences, Clinical Research Certification
Work EnvironmentBiotech companies, R&D labs, manufacturingClinical trial sites, hospitals, pharmaceutical companies
Industry UsageBiotech product development, research projectsClinical trial management, regulatory compliance
Common Search/ComparisonYesYes

The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.

How does a Project Manager in biotech typically collaborate with cross-functional teams to drive project success?

A Project Manager in the biotech sector routinely works with cross-functional teams that include scientists, regulatory experts, manufacturing staff, and quality assurance professionals. They coordinate meetings, align project timelines, and ensure clear communication of goals and milestones. Effective collaboration involves resolving conflicts, facilitating information flow among departments, and adapting plans as scientific or regulatory requirements evolve. This collaborative approach is essential for keeping projects on track, maintaining compliance, and achieving successful outcomes in a highly regulated and fast-paced industry.

What does a Project Manager in Biotech do?

A Project Manager in Biotech is responsible for planning, coordinating, and overseeing projects within biotechnology companies or research organizations. They work closely with scientists, regulatory teams, and other stakeholders to ensure that projects meet deadlines, stay within budget, and comply with industry regulations. Their tasks may include setting project timelines, managing resources, mitigating risks, and communicating progress to leadership. Project Managers play a crucial role in bringing new biotech products or research initiatives from conception to completion.

What are the key skills and qualifications needed to thrive as a Project Manager in Biotech, and why are they important?

To thrive as a Project Manager in Biotech, you need a solid background in life sciences or engineering, experience in project management, and often a relevant degree such as a BSc or MSc, sometimes complemented by a PMP certification. Familiarity with project management software (such as MS Project or Jira), regulatory compliance systems, and budgeting tools is frequently required. Strong leadership, problem-solving, and effective communication skills set standout candidates apart by enabling them to coordinate cross-functional teams and manage complex timelines. These skills are essential to ensure that projects meet regulatory standards, stay on schedule, and achieve scientific and business goals.
What are popular job titles related to Project Manager Biotech jobs in Kansas? For Project Manager Biotech jobs in Kansas, the most frequently searched job titles are:
What job categories do people searching Project Manager Biotech jobs in Kansas look for? The top searched job categories for Project Manager Biotech jobs in Kansas are:
What cities in Kansas are hiring for Project Manager Biotech jobs? Cities in Kansas with the most Project Manager Biotech job openings:
Project Manager Biotech jobs near you
Infographic showing various Project Manager Biotech job openings in Kansas as of June 2026, with employment types broken down into 100% Full Time. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $85,782 per year, or $41.2 per hour.

Senior / Business Development Director, USA

Emerald Clinical Trials

Overland Park, KS • On-site, Remote

Full-time

Posted 18 days ago

Job description

** The job title will be assigned based on the candidate's experience, ranging from Business Development Director to Senior Business Development Director.**
Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world's top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases, offering Phase I-IV and real-world studies.
With over 25 years of experience and a world-renowned focus in renal research, Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality.
Global Expertise. Local Insight. Real Impact.
Emerald Clinical is where science, speed, and strategy come together to transform healthcare. For over 25 years, we have led the way in clinical research, combining global reach with deep Asia-Pacific expertise and unparalleled local insight to deliver smarter trials and stronger outcomes.
Our 800+ employees that span across Asia-Pacific, Europe, and the Americas areembedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward.
About the Role
The Business Development Director will lead the outbound sales strategy to promote our global clinical trial capabilities to biopharmaceutical and biotech companies based in the USA. This role is pivotal in positioning our organization as the CRO of choice for American sponsors seeking to conduct high-quality, cost-efficient clinical trials globally - leveraging our international infrastructure, regulatory expertise, and access to diverse patient populations across North America, APAC, and other key regions. The ideal candidate brings a strong network within USA's life sciences ecosystem, deep knowledge of global clinical development pathways, and a proven track record in selling international CRO services to American clients.
Your Responsibilities
Strategic Business Development
  • Develop and execute a targeted outbound sales plan to drive adoption of our overseas clinical trial solutions among American biotech and pharma companies.
  • Identify and engage American sponsors actively exploring or planning global or multi-regional clinical trials.
  • Position the company as the strategic partner of choice for American innovators seeking to expand into international markets through robust clinical data.

Client Engagement & Relationship Building
  • Proactively connect with decision-makers in American biopharma firms via direct outreach, industry conferences, and professional networks.
  • Lead compelling capability presentations and solution workshops highlighting our global operational footprint, regulatory success stories, and therapeutic expertise.
  • Cultivate long-term relationships with R&D heads, clinical operations leaders, and outsourcing executives at US companies.

Proposal Development & Contract Negotiation
  • Collaborate with internal teams (proposal team, clinical operations, regulatory, biometrics, etc.) to develop tailored proposals and budgets for overseas trials sponsored by American clients.
  • Lead contract negotiations, ensuring alignment with company profitability and legal guidelines.
  • Drive the sales process from lead generation to contract signing.

Market & Competitive Intelligence
  • Track trends in USA's biopharma sector, including outbound investment, globalization strategies, and regulatory.
  • Monitor competitor offerings targeting clients and identify differentiation opportunities.
  • Provide actionable insights to product, marketing, and leadership teams on evolving client demands and market gaps.

Cross-Functional Collaboration
  • Work closely with global project management and clinical delivery teams to ensure seamless transition from sales to study start-up.
  • Collaborate with marketing to create US-focused content-case studies, webinars, and digital campaigns-that showcase successful overseas trial execution for American sponsors.

About You
  • Bachelor's degree in life sciences, medicine, pharmacy, or a related field; advanced degree (MBA, MSc, PhD) preferred.
  • Minimum 8 years of professional experience in the CRO, biotech, or pharmaceutical industry, with a clear focus on selling international clinical trial services to clients. (At least 3 years of working experience in a BD role)
  • Demonstrated success in closing deals with American biopharma companies looking to run trials in the US, EU, or other international markets.
  • Established network within American's biotech and emerging pharma landscape, particularly among innovation-driven companies with global ambitions.
  • Solid understanding of clinical trial design, ICH-GCP standards, and regulatory requirements globally.
  • Self-driven, target-oriented, and comfortable working independently in a fast-paced, global environment.
  • Willingness to travel domestically (up to 40-50%) to meet clients and attend industry events.

Why Join Us?
At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first-both patients and our employees. By joining our team, you'll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.
Here's what makes us stand out:
• Purpose-Driven Work: You'll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.
• Global Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial.
• Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.
What We Offer
We understand that great work happens when people feel valued and supported. That's why we provide:
• Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience.
• Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role.
• Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role.
• Employee Wellbeing: Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events.
• Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients.
Interested? Apply now and help us achieve our mission to improve the health of millions worldwide.
  • We are an equal-opportunity employer and encourage applications from all qualified candidates.

The expected salary range for this position is $150,000 - $200,000 per year, depending on experience and qualifications.
Department Business Development Role Director Business Development Locations Kansas Cit - USA, Memphis - USA, United States Remote status Fully Remote

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