Research Product Manager Jobs in Iowa
Research Product Manager jobs in Iowa are most active in the life sciences, agricultural technology, and financial services sectors, with openings at every level from associate product manager to senior director. Des Moines, Iowa City, and Cedar Rapids account for the largest share of postings, where established employers such as Principal Financial Group, the University of Iowa, and Corteva Agriscience maintain sustained research and product development operations. The most in-demand specialties are clinical research product management, agtech platform development, and data-driven consumer insights. Scan the live roles below and apply to whichever ones fit.
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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 65 Research Product Manager Jobs in Iowa
Find roles in Iowa that match your experience and apply in just a few clicks.
Find Research Product Manager JobsResearch Product Manager Jobs by City in Iowa
Where Iowa roles are concentrated, by current openings.
Research Product Manager Job Market in Iowa
A snapshot from current Iowa openings, updated as new roles post.
Who's Hiring
- The University of Iowa18
- Iowa State University10
- KALCON5
- SSAB3
- Wells Enterprises3
Top Industries Hiring
- Education22
- Manufacturing4
- Food & Beverage4
- Retail3
- Energy2
What Iowa Employers Look For
The qualifications that appear most often in research product manager jobs across Iowa.
- Bachelor's degree in business, life sciences, engineering, or a related technical field
- Three or more years of product management experience within a research or R&D environment
- Demonstrated ability to translate research findings into product roadmaps and go-to-market plans
- Proficiency with agile methodologies, product lifecycle tools, and data analytics platforms
- Strong cross-functional collaboration skills working with scientists, engineers, and commercial teams
- Experience with regulatory or compliance considerations relevant to agricultural, medical, or financial research products
Research Product Manager Jobs in Iowa: Frequently Asked Questions
How do you become a research product manager in Iowa?
Most research product managers in Iowa enter the role through a bachelor's degree in business, engineering, life sciences, or a related technical field, followed by experience in product, research, or program coordination roles. Iowa does not require a state-issued license for this position. Candidates who pursue a Certified Product Manager credential or complete graduate programs at institutions like the University of Iowa's Tippie College of Business or Iowa State University's College of Engineering typically gain a competitive edge with Iowa's research-focused employers.
Which companies hire research product managers in Iowa?
Iowa research product manager roles are posted by The University of Iowa, Iowa State University, and KALCON and others right now, based on current listings on Migrate Mate as of July 2026. Iowa's blend of agricultural technology firms, insurance and financial services headquarters, and major university research centers creates consistent demand for this role across multiple industries.
Which Iowa cities have the most research product manager jobs?
Iowa City, Des Moines, and Ames are the Iowa cities with the most research product manager openings. Des Moines anchors demand through its large concentration of financial services and insurance headquarters, Iowa City draws heavily from University of Iowa health and research operations, and Cedar Rapids benefits from its agribusiness and advanced manufacturing base, which generates steady product management needs tied to R&D pipelines.
Are there remote research product manager jobs in Iowa?
Yes, and more than most fields. About 20% of research product manager openings tied to Iowa are remote or hybrid as of July 2026, reflecting the desk-based and collaborative nature of the role. Strategic and planning-heavy responsibilities such as roadmap development, stakeholder alignment, and data analysis are the most commonly performed remotely, while roles tied to laboratory or clinical research environments tend to require on-site presence.
How can I get hired as a research product manager in Iowa with little or no experience?
The most realistic entry path is moving into a research product manager role from an adjacent position such as research coordinator, business analyst, or associate project manager. Large Iowa employers including Principal Financial Group, Corteva Agriscience, and the University of Iowa Health Care run rotational associate programs and new-graduate development tracks that open doors for candidates without direct product management experience. Building a portfolio of product thinking work, completing a Certified Product Manager course, or earning a graduate certificate in product or innovation management at an Iowa institution strengthens any application at this level.
Where can I find and apply to research product manager jobs in Iowa?
You can find and apply to research product manager jobs in Iowa on Migrate Mate, which lists current Iowa openings in one place. Search the available roles, identify the ones that match your background and preferences, and apply directly to the positions that fit.
See All 65 Research Product Manager Jobs in Iowa
Find roles in Iowa that match your experience and apply in just a few clicks.
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