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Associate Clinical Data Manager Jobs in Iowa (NOW HIRING)

Zimmer Biomet

$14.75 - $19.75/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

Zimmer Biomet

$14.75 - $19.50/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

Zimmer Biomet

$14.75 - $19.75/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of ...

Outcomes

Clinical Program Manager

West Des Moines, IA · On-site

Serve as clinical program data subject matter expert/coordinator to ensure client data files align ... Flex PTO for Exempt Associates & up to 15 PTO days in first year of employment for non-exempt ...

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Associate Clinical Data Manager information

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$36

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

As of Aug 13, 2026, the average hourly pay for associate clinical data manager in Iowa is $36.59, according to ZipRecruiter salary data. Most workers in this role earn between $27.55 and $36.59 per hour, depending on experience, location, and employer.

What does an associate clinical data manager do?

An Associate Clinical Data Manager is responsible for collecting, cleaning, and managing clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They work closely with clinical teams to design data collection tools, monitor data quality, and resolve discrepancies. Their work is crucial in supporting the analysis and reporting of clinical trial results, which can impact decisions about new medical treatments.

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

To thrive as an Associate Clinical Data Manager, you need a solid background in life sciences or related fields, strong analytical abilities, and attention to detail, often supported by a relevant bachelor's degree. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools like Medidata Rave, and an understanding of regulatory guidelines such as ICH-GCP are typically required. Excellent organizational skills, effective communication, and problem-solving abilities help you excel in managing complex datasets and collaborating across teams. These skills ensure data integrity, regulatory compliance, and smooth conduct of clinical trials, which are critical to successful drug development.

What are some common challenges an associate clinical data manager might face when working on multi-site clinical trials?

Associate Clinical Data Managers often encounter challenges such as ensuring data consistency across different trial sites and managing discrepancies that arise from varying data entry practices. Coordinating with site staff, monitoring data quality, and adhering to strict timelines require strong communication and organizational skills. Additionally, adapting to evolving regulatory requirements and new data management technologies can be demanding, but these challenges also offer valuable learning opportunities for career growth.

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

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Associate Clinical Data Manager jobs near you
Infographic showing various Associate Clinical Data Manager job openings in Iowa as of June 2026, with employment types broken down into 1% As Needed, 70% Full Time, 24% Part Time, and 5% Contract. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $76,099 per year, or $36.6 per hour.

Clinical/HC Research Specialist - Otolaryngology

University of Iowa

Iowa City, IA • On-site

Full-time

Re-posted 29 days ago

University Of Iowa rating

6.9

Company rating: 6.9 out of 10

Based on 85 frontline employees who took The Breakroom Quiz

458th of 618 rated colleges and universities

Job description

SUMMARY:
The Cochlear Implant Electrophysiology Laboratory in the Department of Otolaryngology - Carver College of Medicine seeks to hire a Research Audiologist/Project Coordinator to join a dynamic, interdisciplinary team of clinician researchers. Our research aims to expand the diagnostic test battery of auditory function for human cochlear implant candidates and recipients. We use electrophysiological tools to characterize the peripheral auditory system and investigate the association with surgical and performance-based outcomes. In addition to our own institutionally driven research, we frequently support manufacturer trials.
The Research Audiologist will translate clinical skills to research protocols. The individual will work as part of a team with researchers and clinicians from otolaryngology, neurobiology, genetics and communication science and will collaborate with colleagues at external institutions. Responsibilities will include knowledge of and adherence to regulatory guidelines, identification of eligible participants, recruitment/consent, coordination with scheduling, independent audiologic/research assessments (including but not limited to immittance, pure-tone audiometry, speech perception, electrical impedance, electrically evoked compound action potential, electrocochleography, stapedial reflex testing), data management and analysis, detailed documentation and record keeping, and equipment maintenance and troubleshooting. The individual should be comfortable in both surgical and non-surgical settings for intra-operative and post-operative assessments. In addition, the individual will help interpret data from a clinical perspective and will have opportunities to assist in the dissemination of research findings (e.g. development of newsletters, infographics, social media posts, oral presentations, and preparation of manuscripts), and to participate in other activities as required.
BASIC POSITION DESCRIPTION:
Apply clinical audiological skills to evaluate and execute research protocols under the leadership of the director of research. Performs a wide range of routine and advanced audiological tests, as necessary, to determine hearing status. Provide support for researchers by addressing project administrative, management and maintenance tasks related to the setting of a hearing research laboratory. Other duties may be required and assigned at times as determined by a supervisor in order to meet the needs of the organization.
KEY AREAS OF RESPONSIBILITY:
Research/Clinical Activities:
  • Perform clinical/health care research activities and functions as a specialist/technical expert in Audiology.
  • Coordinate the care of research participants according to protocols requiring a high level of judgment and independent action.
  • Review new protocols and assign protocols to staff.

Protocol Development/Management of Study Responsibilities:
  • Develop, edit, coordinate, manage and maintain protocols.
  • Establish study-related metrics for efficiency and success.
  • Prepare, evaluate and analyze reports.
  • Review aggregate data from query resolutions and monitor visit reports for all studies.
  • Responsible for site management and daily activities associated with clinical trials.
  • Provide training and guidance; organize and facilitate meetings.
  • Communicate to health care practitioners, agencies and sponsors.
  • Ensure human subjects protection.
  • Provide care that is safe, effective and efficient.

Data Collection and Monitoring:
  • Evaluate and analyze data collection procedures and data.
  • Update and maintain the requirements and specifications for the electronic data capture systems.

Regulatory Guidelines and Documents:
  • Manage safety of subjects/patients.
  • Assume responsibility for reportable events reporting, and any corrective actions taken.
  • Manage and organize regulatory documentation.
  • Prepare regulatory submissions.
  • Perform on-site audits of research and clinical data.
  • Communicate with IRB staff and investigators.

Human Resources/Leadership:
  • May hire, develop and manage the performance of staff; assure staff is complaint with UI policies and procedures.
  • May develop, implement and expand education and training activities.

Financial Responsibility:
  • Perform administrative tasks to assure completion within specific timelines and budgets.
  • Develop and administer budget for studies.

Facilities and Equipment Management:
  • Assist in the management and maintenance of lab equipment including software updates and calibration.
  • Troubleshoot issues and navigate repairs.
  • Create and maintain logs of laboratory owned and manufacturer loaned equipment.
  • Set up and operate research materials and equipment.
  • Assist with the procurement of supplies and materials.

SUPERVISION RECEIVED
Supervision will be provided from the study investigator, Dr. Rachel Scheperle (Department of Otolaryngology), with oversite from Dr. Marlan Hansen (Department of Otolaryngology).
SUPERVISION EXERCISED
May supervise and/or facilitate the progress of trainees working on research projects.
Required Qualifications:
  • Masters or doctoral audiology (AuD) degree from an accredited university.
  • Valid Audiology license in the state of Iowa.
  • At least 3 years of related experience.
  • Excellent interpersonal and written and verbal communication skills.
  • Excellent command of the English language, both written and verbal.
  • Attention to detail, accuracy, and strong organizational skills.
  • Scheduling flexibility to accommodate surgical schedules, subject preferences and research deadlines (The position is 8:00 am-5:00 pm with frequent 7:00 am start times and occasional evening or weekend hours).
  • Capable of teamwork and ability to work independently.
  • Demonstrated knowledge of effective strategies for working with faculty, staff, and students from a variety of backgrounds and perspectives.

Desirable Qualifications:
  • American Speech-Language-Hearing Association certification or eligibility.
  • Clinical and/or research experience working with cochlear implant recipients, cochlear implant programming, and intraoperative monitoring.
  • Experience with cochlear implant programming software (Soundwave, Target, CustomSound, Maestro, BEDCS, NIC, RIB).
  • Experience with research software (e.g. Matlab, Python, SigmaPlot, LabView, R, etc.)
  • Experience contributing to manuscripts and presenting at conferences.
  • Experience supervising audiology students in clinical or research practicums.

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 ashley-rayer@uiowa.edu.

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