Senior Clinical Project Manager Jobs in Iowa
Senior Clinical Project Manager jobs in Iowa are concentrated in clinical research, pharmaceutical development, and health system operations, with demand anchored by the state's academic medical centers, contract research organizations, and growing biopharma sector. The busiest hiring markets are Des Moines, Iowa City, and Cedar Rapids, where employers like the University of Iowa Health Care, UnityPoint Health, and Hy-Vee Health have established and lasting clinical operations. The most in-demand specialties include oncology trial management, multi-site study coordination, and regulatory affairs oversight. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 338+ Senior Clinical Project Manager jobs
To manage and support clinical trial regulatory activities for the Pediatric Department, Clinical Research Services. Act as back-up study coordinator for studies as appropriate.
This is a specified term position.
Duties to include:
Take primary responsibility in collaboration with study lead coordinator to complete regulatory activities to open new clinical trials.
Serve as a resource and support to study coordinators for regulatory activities required to maintain and close clinical trials.
Coordinate specific aspects of external review and internal processes. Specifically, oversee the preparation and submission of the appropriate Human Subjects Review forms and application materials to the Institutional Review Board (IRB-01), and central IRB entities. Collaborate with study-specific coordinator to prepare consent forms for research protocols and local and central IRB submissions.
Prepare and submit application forms and serve as liaison to the Clinical Research Unit (CRU), the Pharmacy and Therapeutics Committee, the Medical Radiation Protection Committee, the Protocol Review and Monitoring Committee, Joint Office of Compliance, Nursing Research Committee, Pathology Committee, and other review committees as necessary.
Support the primary study coordinator(s) as needed on additional regulatory tasks (such as annual reviews, modifications, Adverse Events, Safety Reports and other reportable events to IRB).
Coordinate the regulatory process and document preparation used in the implementation of clinical trials.
Serve as liaison to clinicians, research investigators, data managers, nursing services staff, pharmacists and medical personnel to ensure sufficient cooperation among participating stakeholders for each clinical research study. Assist in the execution, administration and maintenance of protocols and clinical studies. Provide input into descriptions of research procedures.
Coordinate specific aspects of external review and align with internal processes. Manage and organize regulatory documentation from sites and regulatory authorities. Prepare regulatory submissions and assist with on-site audits when needed.
Monitor compliance with regulatory guidelines and ensure proper maintenance of documents. Work with primary coordinator to develop regulatory files and binders, assist as requested in maintenance.
Assist primary study coordinator(s) with monitoring and auditing issues that relate to regulatory activities, when needed.
Enter data for the evaluation of clinical research metrics through our OnCore database as it relates to the initial regulatory review and submission process.
Assist study staff with compliance of policies and procedures as they relate to regulatory activities.
Prepare and deliver basic content that enhances knowledge of and compliance with internal and external standards and regulations.
Attend all appropriate meetings as assigned: this will include but is not limited to with internal and external groups to provide reporting of study updates, educational and training meetings, meetings with team leads and supervisors, and meetings with sponsors or CROs.
Assist in general coordinator activities as required as a back-up coordinator. These might include study-specific training, assist with preparing for and completing subject visits, data entry, and other study specific tasks as appropriate.
Education Requirements
- A Bachelor’s Degree or an equivalent combination of education and experience
Required Qualifications
Excellent written, verbal and interpersonal communication skills
Excellent organizational and time management skills
Proficient in computer software applications including spreadsheet and database experience
Experience in coordinating multiple projects and various functions independently
Prior experience with Institutional Review Board application materials and processing
Knowledge of regulations that apply to human research
Proven ability to utilize medical terminology
Desired Qualifications
Experience working in a research facility with protocols or management of clinical data, i.e., laboratory values, toxicity levels
1-3 years administrative and/or program management experience
Knowledge of University of Iowa policies, procedures and regulations
Position and Application details:
In order to be considered for an interview, applicants must upload the following documents and mark them as a “Relevant File” to the submission:
Resume
Cover Letter
Job openings are posted for a minimum of 7 calendar days and may be removed from posting and filled any time after the original posting period has ended.
Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to 5 professional references will be requested at a later step in the recruitment process.
For additional questions, please contact pedsuichildrenshr@healthcare.uiowa.edu
This position is not eligible for University sponsorship for employment authorization.
- Classification Title: Clin Trials Rsrch Asst/Data Mg
- Appointment Type: Professional and Scientific
- Schedule: Full-time
- Work Modality Options: On Campus
- Pay Level: 3A
- Organization: Healthcare
- Contact Name: Natasha Johnson
- Contact Email: pedsuichildrenshr@healthcare.uiowa.edu
To manage and support clinical trial regulatory activities for the Pediatric Department, Clinical Research Services. Act as back-up study coordinator for studies as appropriate.
This is a specified term position.
Duties to include:
Take primary responsibility in collaboration with study lead coordinator to complete regulatory activities to open new clinical trials.
Serve as a resource and support to study coordinators for regulatory activities required to maintain and close clinical trials.
Coordinate specific aspects of external review and internal processes. Specifically, oversee the preparation and submission of the appropriate Human Subjects Review forms and application materials to the Institutional Review Board (IRB-01), and central IRB entities. Collaborate with study-specific coordinator to prepare consent forms for research protocols and local and central IRB submissions.
Prepare and submit application forms and serve as liaison to the Clinical Research Unit (CRU), the Pharmacy and Therapeutics Committee, the Medical Radiation Protection Committee, the Protocol Review and Monitoring Committee, Joint Office of Compliance, Nursing Research Committee, Pathology Committee, and other review committees as necessary.
Support the primary study coordinator(s) as needed on additional regulatory tasks (such as annual reviews, modifications, Adverse Events, Safety Reports and other reportable events to IRB).
Coordinate the regulatory process and document preparation used in the implementation of clinical trials.
Serve as liaison to clinicians, research investigators, data managers, nursing services staff, pharmacists and medical personnel to ensure sufficient cooperation among participating stakeholders for each clinical research study. Assist in the execution, administration and maintenance of protocols and clinical studies. Provide input into descriptions of research procedures.
Coordinate specific aspects of external review and align with internal processes. Manage and organize regulatory documentation from sites and regulatory authorities. Prepare regulatory submissions and assist with on-site audits when needed.
Monitor compliance with regulatory guidelines and ensure proper maintenance of documents. Work with primary coordinator to develop regulatory files and binders, assist as requested in maintenance.
Assist primary study coordinator(s) with monitoring and auditing issues that relate to regulatory activities, when needed.
Enter data for the evaluation of clinical research metrics through our OnCore database as it relates to the initial regulatory review and submission process.
Assist study staff with compliance of policies and procedures as they relate to regulatory activities.
Prepare and deliver basic content that enhances knowledge of and compliance with internal and external standards and regulations.
Attend all appropriate meetings as assigned: this will include but is not limited to with internal and external groups to provide reporting of study updates, educational and training meetings, meetings with team leads and supervisors, and meetings with sponsors or CROs.
Assist in general coordinator activities as required as a back-up coordinator. These might include study-specific training, assist with preparing for and completing subject visits, data entry, and other study specific tasks as appropriate.
Education Requirements
- A Bachelor’s Degree or an equivalent combination of education and experience
Required Qualifications
Excellent written, verbal and interpersonal communication skills
Excellent organizational and time management skills
Proficient in computer software applications including spreadsheet and database experience
Experience in coordinating multiple projects and various functions independently
Prior experience with Institutional Review Board application materials and processing
Knowledge of regulations that apply to human research
Proven ability to utilize medical terminology
Desired Qualifications
Experience working in a research facility with protocols or management of clinical data, i.e., laboratory values, toxicity levels
1-3 years administrative and/or program management experience
Knowledge of University of Iowa policies, procedures and regulations
Position and Application details:
In order to be considered for an interview, applicants must upload the following documents and mark them as a “Relevant File” to the submission:
Resume
Cover Letter
Job openings are posted for a minimum of 7 calendar days and may be removed from posting and filled any time after the original posting period has ended.
Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification. Up to 5 professional references will be requested at a later step in the recruitment process.
For additional questions, please contact pedsuichildrenshr@healthcare.uiowa.edu
This position is not eligible for University sponsorship for employment authorization.
- Classification Title: Clin Trials Rsrch Asst/Data Mg
- Appointment Type: Professional and Scientific
- Schedule: Full-time
- Work Modality Options: On Campus
- Pay Level: 3A
- Organization: Healthcare
- Contact Name: Natasha Johnson
- Contact Email: pedsuichildrenshr@healthcare.uiowa.edu
See All 338+ Senior Clinical Project Manager Jobs in Iowa
Find roles in Iowa that match your experience and apply in just a few clicks.
Find JobsSenior Clinical Project Manager Jobs by City in Iowa
Where Iowa roles are concentrated, by current openings.
Senior Clinical Project Manager Job Market in Iowa
A snapshot from current Iowa openings, updated as new roles post.
Who's Hiring
- The University of Iowa34
- Collins Aerospace16
- UnityPoint Health15
- Iowa State University10
- Mercy Cedar Rapids8
Top Industries Hiring
- Healthcare & Medical Services50
- Education44
- Insurance11
- Technology & Software11
- Aerospace & Defense10
What Iowa Employers Look For
The qualifications that appear most often in senior clinical project manager jobs across Iowa.
- Bachelor's or master's degree in life sciences, nursing, or a related clinical field
- Five or more years of clinical trial or clinical operations project management experience
- PMP, CAPM, or equivalent project management certification strongly preferred by Iowa employers
- Demonstrated experience managing Phase II through Phase IV clinical studies across multiple sites
- Proficiency with clinical trial management systems such as Medidata Rave or Veeva Vault
- Strong knowledge of ICH-GCP guidelines, FDA regulations, and IRB submission processes
Senior Clinical Project Manager Jobs in Iowa: Frequently Asked Questions
How do you become a senior clinical project manager in Iowa?
The typical path in Iowa is a bachelor's degree in a health science or life science field followed by several years in clinical trial coordination or clinical operations, often starting at Iowa academic medical centers or contract research organizations. There is no Iowa-specific state license required for this role, but employers consistently favor candidates who hold a Project Management Professional certification and have direct experience with FDA-regulated clinical studies. Building experience at institutions like the University of Iowa's clinical research offices is a recognized stepping stone.
How much do senior clinical project managers make in Iowa?
Senior clinical project managers in Iowa earn a median of about $96,540 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $62,000 for the lowest 10% to over $150,290 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire senior clinical project managers in Iowa?
Employers hiring senior clinical project managers in Iowa right now include The University of Iowa, Collins Aerospace, and UnityPoint Health, based on current listings on Migrate Mate as of July 2026. Iowa's mix of academic health systems, regional hospital networks, and emerging biopharma companies means openings appear across both large institutions and specialized clinical research organizations operating in the state.
Which Iowa cities have the most senior clinical project manager jobs?
Des Moines, Iowa City, and Cedar Rapids account for the largest share of senior clinical project manager openings in Iowa. Des Moines drives volume through its major health system headquarters and growing life sciences corridor, Iowa City concentrates demand around the University of Iowa Health Care and its affiliated clinical research programs, and Cedar Rapids reflects the presence of regional hospital networks and contract research operations expanding along the Interstate 380 corridor.
Are there remote senior clinical project manager jobs in Iowa?
Yes, and more than many clinical roles, because senior clinical project managers spend a significant portion of their work in documentation, vendor oversight, and stakeholder communication rather than direct patient care. About 34% of senior clinical project manager openings tied to Iowa are remote or hybrid as of July 2026, reflecting the desk-heavy and coordination-focused nature of the role. Fully remote positions are most common for regulatory affairs oversight and multi-site program management, while roles requiring on-site monitoring visits remain hybrid.
How can I get hired as a senior clinical project manager in Iowa with little or no experience?
The most realistic entry path is starting as a clinical research coordinator or clinical trial assistant at an Iowa academic medical center or regional hospital, then building toward a project management role. The University of Iowa Health Care and UnityPoint Health regularly hire research coordinators at the entry level, giving candidates direct exposure to FDA-regulated trials. Earning a Certified Clinical Research Coordinator credential through ACRP or SOCRA alongside an entry-level role signals readiness to move into project oversight, and candidates who document protocol deviations and site management experience position themselves well for promotion.
Where can I find and apply to senior clinical project manager jobs in Iowa?
You can find and apply to senior clinical project manager jobs in Iowa on Migrate Mate, which lists current Iowa openings in one place. Search the listings, find the roles that match your experience and location preferences, and apply directly to whichever ones fit.
See All 338+ Senior Clinical Project Manager Jobs in Iowa
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