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Biotechnology Project Manager Jobs in Kansas (NOW HIRING)

Premier Research

$122K/yr

Premier Research is looking for a Senior Project Manager, Dermatology to join our General Medicine ... You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and ...

Eversana

Sr. Project Manager

Overland Park, KS · On-site

... biotech start-ups to established pharmaceutical companies. Our products, services and solutions ... As a Senior IT Project Manager, you will be responsible for managing project lifecycles ...

Iff

Manage internal resources and external engineering and construction partners to ensure scope ... BioTech) or equivalent technical experience * 2+ years of experience executing capital projects in ...

Merck Group

Principal Project Engineer

Lenexa, KS · On-site

$106K - $172K/yr

This includes technical project management for both capital projects and process improvements. You ... Experience in medical, biotechnology, or Bio-pharmaceutical manufacturing environment is highly ...

New

IQVIA

CRA 1, IQVIA Biotech

Overland Park, KS

$71K - $145K/yr

The ability to manage multiple tasks, prioritize effectively, and work independently while ... Ability to travel as required by the project. IQVIA is a leading global provider of clinical ...

Intellectt INC

Process Engineer

Kansas City, KS · On-site

We are seeking a Process Engineer with 3-7 years of experience in pharmaceutical, biotechnology ... CAPA, Change Control, and Deviation Management * Data Analysis and Continuous Improvement Required ...

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Biotechnology Project Manager information

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$19

$41

$68

How much do biotechnology project manager jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for biotechnology project manager 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 does a biotechnology project manager do?

A Biotechnology Project Manager oversees and coordinates projects within the biotechnology industry, ensuring that research and development initiatives, product launches, or clinical trials are completed on time and within budget. They work with cross-functional teams, including scientists, engineers, and regulatory experts, to set project goals, manage resources, and monitor progress. Their responsibilities also include risk management, stakeholder communication, and ensuring compliance with industry regulations. This role is vital for driving innovation and bringing new biotech products or solutions to market efficiently.

What is the difference between Biotechnology Project Manager vs Research Scientist?

AspectBiotechnology Project ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Project Management certification often preferredMaster's or PhD in Biotechnology or related field
Work EnvironmentProject teams, corporate labs, industry settingsResearch labs, academic institutions, industry research divisions
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech startupsUniversities, research institutes, biotech companies

The main difference is that a Biotechnology Project Manager oversees project planning, coordination, and execution within biotech companies, focusing on timelines and budgets. In contrast, a Research Scientist conducts experiments and develops new biotech products or knowledge. Both roles require strong biotech credentials, but their daily tasks and focus areas differ significantly.

What are the key skills and qualifications needed to thrive as a biotechnology project manager, and why are they important?

To thrive as a Biotechnology Project Manager, you need a solid background in biological sciences or engineering, project management expertise, and often an advanced degree such as an MSc or PhD. Familiarity with tools like Microsoft Project, Gantt charts, regulatory compliance systems, and certifications such as PMP are commonly required. Strong leadership, communication, and problem-solving skills set exceptional candidates apart in managing cross-functional teams and complex timelines. These skills and qualities are essential to effectively coordinate scientific projects, ensure regulatory compliance, and deliver successful outcomes in a dynamic biotech environment.

What are some common challenges faced by biotechnology project managers in cross-functional team environments?

Biotechnology Project Managers often work with multidisciplinary teams composed of scientists, regulatory specialists, manufacturing experts, and business development professionals. One common challenge is ensuring clear communication and alignment across these diverse groups, especially when technical jargon or differing priorities create misunderstandings. Additionally, managing project timelines in a highly regulated environment, where unexpected trial results or compliance issues may cause delays, requires strong adaptive planning. Successful Biotechnology Project Managers foster collaboration by setting clear goals, conducting regular check-ins, and proactively addressing potential roadblocks.
What are popular job titles related to Biotechnology Project Manager jobs in Kansas? For Biotechnology Project Manager jobs in Kansas, the most frequently searched job titles are:
What job categories do people searching Biotechnology Project Manager jobs in Kansas look for? The top searched job categories for Biotechnology Project Manager jobs in Kansas are:
What cities in Kansas are hiring for Biotechnology Project Manager jobs? Cities in Kansas with the most Biotechnology Project Manager job openings:
Biotechnology Project Manager jobs near you
Infographic showing various Biotechnology Project Manager job openings in Kansas as of July 2026, with employment types broken down into 5% Internship, 77% Full Time, 11% Part Time, 1% Temporary, 3% Contract, and 3% Summer. Highlights an 76% Physical, 2% Hybrid, and 22% Remote job distribution, with an average salary of $85,782 per year, or $41.2 per hour.

Sr. Clinical Project Manager, IQVIA Biotech

IQVIA

Overland Park, KS • On-site

$93K - $232K/yr

Full-time

Re-posted 19 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

59th of 221 rated it services

Job description

IQVIA Biotech is seeking a Sr. Clinical Project Manager with experience in the following therapeutics: Cardiovascular, Renal, and Metabolic.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Overview
The Senior Clinical Project Manager is a key leader in the delivery of clinical trials, partnering with cross-functional teams and clients to accelerate the development of life-changing therapies. This role is responsible for end-to-end clinical study execution, ensuring projects are delivered on time, within scope, and on budget, while maintaining the highest standards of quality and compliance. The Senior Clinical Project Manager provides strategic oversight, operational leadership, and serves as the primary point of contact for sponsors.

Key Responsibilities

  • Lead the planning, execution, and delivery of medium to large, multi-regional clinical studies in alignment with contractual requirements, SOPs, and regulatory standards.
  • Develop and implement integrated study management plans, ensuring consistency in processes, tools, and training.
  • Serve as the primary liaison with sponsors, building strong client relationships and ensuring transparent communication on project status, risks, and deliverables.
  • Set direction and objectives for cross-functional project teams; monitor performance and drive accountability to meet milestones.
  • Partner with Business Development on bid defenses and contribute to winning new business, including leading presentations when applicable.
  • Proactively identify, assess, and mitigate risks; lead issue resolution and implement corrective and preventative action plans.
  • Collaborate with internal functional groups to support study execution and overcome operational challenges.
  • Monitor project progress against timelines, budget, and quality metrics; provide regular updates to internal and external stakeholders.
  • Ensure financial performance by managing budgets, forecasting revenue, and identifying opportunities to accelerate delivery.
  • Manage scope changes and oversee change control processes in collaboration with stakeholders.
  • Promote continuous improvement by sharing lessons learned and best practices.
  • Mentor and support the development of junior team members and contribute feedback on team performance.

Qualifications

  • Bachelor's Degree in Life Sciences or a related field required; advanced degree preferred.
  • Requires greater than 7 years of clinical research experience, including at least 4 years of project management experience, or an equivalent combination of education, training, and experience.
  • Proven ability to manage complex, global clinical trials and cross-functional teams.
  • Strong leadership, communication, and stakeholder management skills.
  • Demonstrated ability to manage budgets, timelines, and risk proactively.
  • Experience leading bid defenses and client engagements is preferred.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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