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$47K

$80.8K

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How much do clinical research project manager jobs pay per year?

As of Sep 3, 2026, the average yearly pay for clinical research project manager in Iowa is $80,806.00, according to ZipRecruiter salary data. Most workers in this role earn between $67,200.00 and $85,900.00 per year, depending on experience, location, and employer.

What does a clinical research project manager do?

A Clinical Research Project Manager oversees the planning, execution, and management of clinical research studies. They coordinate teams, ensure regulatory compliance, manage budgets and timelines, and act as a liaison between stakeholders such as sponsors, investigators, and regulatory agencies. Their primary goal is to ensure that clinical trials are conducted efficiently, ethically, and according to protocol. This role requires strong organizational, leadership, and communication skills, as well as a deep understanding of clinical research processes.

What are the key skills and qualifications needed to thrive as a clinical research project manager?

To thrive as a Clinical Research Project Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with tools such as CTMS (Clinical Trial Management Systems), EDC (Electronic Data Capture), and certifications like PMP or ACRP-PM is highly valuable. Strong leadership, communication, and problem-solving skills help you coordinate teams and manage stakeholder expectations. These competencies are crucial to ensure trials are conducted efficiently, ethically, and in line with regulatory standards.

What are some common challenges faced by clinical research project managers and how can they be addressed?

Clinical Research Project Managers often encounter challenges such as managing complex timelines, ensuring regulatory compliance, and coordinating communication between diverse stakeholders. Balancing the needs of sponsors, research teams, and regulatory bodies requires strong organizational and problem-solving skills. Staying proactive with risk management and fostering clear, consistent communication can help address these challenges effectively. Leveraging project management tools and regularly scheduled check-ins also supports smoother project execution and team collaboration.

What is the difference between Clinical Research Project Manager vs Clinical Research Coordinator?

AspectClinical Research Project ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsBachelor's in health sciences or related field, often with clinical research certifications
Work EnvironmentOversees multiple projects, manages teams, and liaises with sponsorsConducts daily clinical trial activities, interacts directly with participants and site staff
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch hospitals, clinics, academic institutions

The Clinical Research Project Manager focuses on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day activities at trial sites, ensuring protocol adherence and participant safety. Both roles are essential but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Research Project jobs in Iowa?

The most popular types of Clinical Research Project jobs in Iowa are:

What are popular job titles related to Clinical Research Project Manager jobs in Iowa?

For Clinical Research Project Manager jobs in Iowa, the most frequently searched job titles are:

What job categories do people searching Clinical Research Project Manager jobs in Iowa look for?

The top searched job categories for Clinical Research Project Manager jobs in Iowa are:

What cities in Iowa are hiring for Clinical Research Project Manager jobs?

Cities in Iowa with the most Clinical Research Project Manager job openings:

Clinical Research Project Manager jobs near you
Infographic showing various Clinical Research Project Manager job openings in Iowa as of August 2026, with employment types broken down into 1% As Needed, 85% Full Time, 13% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $80,806 per year, or $38.8 per hour.

Clinical Laboratory Research Scientist

Elanco Animal Health Incorporated

Fort Dodge, IA • On-site

Full-time

Retirement, PTO

Re-posted 8 days ago

Elanco rating

7.8

Company rating: 7.8 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

50th of 86 rated pharmaceutical

Job description

At Elanco (NYSE: ELAN) - it all starts with animals!
As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose - all to Go Beyond for Animals, Customers, Society and Our People.
At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
Making animals' lives better makes life better - join our team today!
Your Role: Clinical Laboratory Research Scientist
As a Research Scientist on our Clinical Development Sciences team, you will play a crucial role in advancing Elanco's pipeline. You will be at the forefront of supporting our ongoing clinical studies by planning, conducting, and meticulously documenting pivotal laboratory experiments. This position offers a unique opportunity to not only contribute to the statistical analysis of clinical trials but also to drive innovation by identifying and applying new technologies to enhance our clinical laboratory capabilities.
Your Responsibilities:
  • Experimental Design & Execution: Work with Sponsors and Study Managers to define project requirements; develop and review protocols, validation methods, and sample analysis plans to support clinical studies (GRP).
  • Methodology & Innovation: Identify, develop, and implement new viral/bacterial culture methodologies, analytical methods, and laboratory technologies to continuously update and improve the clinical laboratory's capabilities.
  • Data Integrity & Analysis: Independently review, approve, and prepare raw data and laboratory data packages for statistical analysis, ensuring scientific accuracy, completeness, and compliance with all quality systems and standards (e.g., GxP, SOPs).
  • Technical Leadership & Support: Lead troubleshooting efforts to resolve scientific issues, manage complex project workloads, and provide technical support to ensure the successful and timely completion of studies.
  • Laboratory Operations: Maintain the laboratory infrastructure, including equipment and a clean, safe, and organized working environment, while preparing and updating SOPs and working procedures.

What You Need to Succeed (minimum qualifications):
  • Education: Bachelor's Degree in Biology, Microbiology, Immunology, Animal Science, or a related scientific discipline with equivalent experience.
  • Experience: A minimum of 5-8 years of hands-on experience in a laboratory setting.
  • Top Skills: Demonstrated experience in laboratory techniques (such as cell culture, assay design, and molecular biology) and a strong understanding of experimental design and data analysis.

What will give you a competitive edge (preferred qualifications):
  • Advanced degree (Master's or PhD) in a relevant scientific discipline.
  • In-depth knowledge of clinical laboratory study design, execution, and operational workflow in a GxP-regulated environment.
  • Excellent communication and interpersonal skills, with proven ability to collaborate effectively in a team setting and present complex scientific data.
  • Experience in leading troubleshooting efforts, managing complex projects, or mentoring junior scientists.

Additional Information:
  • Travel: Less than 10%
  • Location: Fort Dodge, IA - On-Site Work Environment

Don't meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
  • Multiple relocation packages
  • Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO)
  • 8-week parental leave
  • 9 Employee Resource Groups
  • Annual bonus offering
  • Flexible work arrangements
  • Up to 6% 401K matching

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job-related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.

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