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Associate Clinical Project Manager Jobs in Iowa (NOW HIRING)

Servpro Industries, Inc.

Project Manager

Mason City, IA · On-site

$60 - $80/hr

As the Restoration Project Manager , you will oversee all aspects of assigned restoration projects ... Associate degree or Bachelor's degree preferred * At least 1 year of management and/or supervisory ...

E2 Optics

Project Manager

Cedar Rapids, IA · On-site

Manage project scheduling requirements to control costs and meet contract requirements * Manage ... High school diploma or GED with experience required, associate or bachelors degree preferred

E2 Optics

Project Manager

Cedar Rapids, IA · On-site

Manage project scheduling requirements to control costs and meet contract requirements * Manage ... High school diploma or GED with experience required, associate or bachelors degree preferred

UIOWA

Senior Project Manager

Iowa City, IA · On-site

... clinical operations. The incumbent may independently lead one or multiple medium to large-sized ... Set and continually manage project expectations with team members and other stakeholders; delegate ...

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Associate Clinical Project Manager information

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$15

$36

$56

How much do associate clinical project manager jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for associate clinical project manager in Iowa is $36.40, according to ZipRecruiter salary data. Most workers in this role earn between $27.98 and $42.21 per hour, depending on experience, location, and employer.

What is an associate clinical project manager?

An Associate Clinical Project Manager (ACPM) is an entry- to mid-level professional who assists in planning, coordinating, and overseeing clinical trials and research projects within pharmaceutical, biotech, or clinical research organizations. They work closely with project managers and cross-functional teams to ensure studies are conducted according to protocol, regulatory requirements, and timelines. ACPMs may handle tasks such as tracking project progress, supporting site management, preparing documentation, and communicating with stakeholders. Their role helps ensure the smooth execution and delivery of clinical research projects.

What are the key skills and qualifications needed to thrive as an associate clinical project manager?

To thrive as an Associate Clinical Project Manager, you need a solid understanding of clinical research processes, project management principles, and typically a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often required. Exceptional organizational skills, attention to detail, and strong communication abilities help you coordinate teams and timelines effectively. These competencies are crucial for ensuring clinical trials run smoothly, meet regulatory standards, and deliver reliable results on schedule.

What are the common challenges faced by an associate clinical project manager and how can they be addressed?

Associate Clinical Project Managers often encounter challenges such as balancing multiple study timelines, coordinating cross-functional teams, and ensuring regulatory compliance. Managing communication between sponsors, vendors, and internal teams can also be complex. To address these challenges, it's important to prioritize tasks, maintain clear documentation, and foster strong relationships with stakeholders. Leveraging project management tools and regularly reviewing project milestones can help ensure studies stay on track and issues are promptly resolved.

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

AspectAssociate Clinical Project ManagerClinical Project Coordinator
CredentialsBachelor's degree, often some project management or clinical research experienceBachelor's degree, entry-level in clinical research
Work EnvironmentSupports project managers, involved in planning and oversightAssists with daily tasks, data collection, and site communication
Employer & Industry UsagePharmaceutical, biotech, clinical research organizationsClinical research sites, CROs, pharma companies

The Associate Clinical Project Manager typically has more responsibility in project planning and oversight compared to the Clinical Project Coordinator, who mainly supports data collection and site coordination. Both roles are essential in clinical research teams, with the associate role often serving as a stepping stone to more senior project management positions.

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

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

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

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

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

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

Associate Clinical Project Manager jobs near you
Infographic showing various Associate Clinical Project Manager job openings in Iowa as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $75,702 per year, or $36.4 per hour.

Project Manager - Clinical Trials

Coralville, IA • On-site

VIDA Diagnostics
11 - 50 employees
Learn more about VIDA Diagnosticsexternal

Full-time

Re-posted 9 days ago

Job description

VIDA is seeking a Clinical Trial Project Manager to act as project lead for global clinical trials using medical imaging. The position interacts with CROs and trial sites and manages the timeline and all project deliverables. Are you interested in delivering effective, end-to-end collaboration, project management, and resource planning to accelerate the global development of safe and effective medical therapeutics? If so, this opportunity is for you. 

Responsibilities: 

The Clinical Trial Project Manager will work cross-functionally at VIDA to support needs of clinical site, and work to meet goals and timelines of Sponsor, including ensuring imaging study objectives, deliverables and schedule meet Sponsor’s needs; Coordinate and manage project start-up, project maintenance, and project close-out activities; Maintain ongoing Sponsor contact for project-specific issues by serving as primary contact for Sponsor and all project team members; 

  • Track study status and progress according to milestones, identify and anticipate potential issues/risks or challenges, and work with team to develop appropriate solutions; 
  • Develop trial management “charter”, including defining KPIs, scheduling and resource plan, risk management plan, communication plan, and other study-specific documents and management tools; 
  • Assess impact of change in scope, and communicate to Sponsor clinical team and VIDA team members; 
  • Accurately report on project status/metrics both for status and as input to finance for invoicing purposes 
  • May be responsible for other projects and responsibilities as assigned 

Qualifications 

  • Bachelor’s degree in Life Sciences or related field and a minimum of 3 years of related imaging or medical device industry experience (i.e. project management), or Master’s degree in Life Sciences or related field and minimum 2 years related imaging or medical device industry experience 
  • Prior experience with clinical trials or working at or with CROs is preferred
  • Exceptional communication skills (oral and written)
  • High attention to detail and quality standard
  • Strong time and project management skills
  • Demonstrated skills managing risk in a reasonable fashion
  • Working knowledge of Good Clinical Practice for clinical trials in the US (21 CFR 812 and other sections) and/or Europe (ISO 14155), and local regulations is preferred; and 
  • Proficient with all Microsoft Office applications (Word, Excel, Power Point, Project, etc.). 

All VIDA employees expected to be flexible and have an entrepreneurial mindset.  Other duties may be assigned as needed. 

VIDA is an equal opportunity employer.  Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, veteran’s status, age or disability.