ZipRecruiter

Log In

1

Clinical Data Associate Jobs in Stillwater, MN (NOW HIRING)

next page

Showing results 1-20

All JobsClinical Data Associate JobsClinical Data Associate Jobs in Stillwater, MN

Clinical Data Associate information

See Stillwater, MN salary details

$14

$40

$90

How much do clinical data associate jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for clinical data associate in Stillwater, MN is $40.63, according to ZipRecruiter salary data. Most workers in this role earn between $30.58 and $40.62 per hour, depending on experience, location, and employer.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

What are the key skills and qualifications needed to thrive as a clinical data associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

What is the difference between Clinical Data Associate vs Clinical Research Coordinator?

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

More about Clinical Data Associate jobs

What cities near Stillwater, MN are hiring for Clinical Data Associate jobs?

Cities near Stillwater, MN with the most Clinical Data Associate job openings:

Clinical Data Associate jobs near you

Associate Director Senior Data Analyst (Clinical Sciences)

BioNTech SE

Saint Paul, MN • On-site

$146K - $234K/yr

Full-time

Re-posted 29 days ago

Key responsibilities

  • Represent DDI as data analyst and technical SME across Clinical functional areas

  • Document Data Transfer Agreements (DTAs) and define data transformation logic

  • Support planning, implementation, onboarding, and operational management of clinical systems and solutions

Job description

Munich, Germany; Cambridge, US; Gaithersburg, US; Mainz, Germany; New Jersey, US | full time | Job ID: 11529
About the role
As Associate Director, Senior Data Analyst liaises with Clinical Science to understand business needs and identify solutions that align to overall strategies. Reviews, analyzes and evaluates business systems and user needs while acting as a technical SME in Clinical Data and Analytics.
Your main responsibilities
  • Represent DDI as data analyst and technical SME across Clinical functional areas
  • Document Data Transfer Agreements (DTAs) for external data exchange
  • Define and document data transformation logic and support implementation
  • Partner with Clinical stakeholders to evaluate business systems and needs
  • Support planning, prioritization, delivery, and operations of Clinical solutions
  • Develop and maintain process documentation (current and to-be)
  • Define system, functional, and business requirements
  • Provide technical SME support for clinical systems (EDC, Elluminate, Databricks, analytics tools)
  • Support implementation and onboarding of new Clinical solutions
  • Manage vendor interactions and ensure service delivery and troubleshoot system and operational issues
  • Coordinate service operations and SLA compliance, support Computer System Validation (CSV) and GxP processes
  • Maintain validation documentation (URS, IQ/OQ/PQ, traceability, reports) and ensure alignment with quality systems and operational procedures

What you have to offer
  • Bachelor's or higher degree in a relevant scientific or technical field
  • 10 -12+ years experience in Clinical Operations/Data Management
  • Strong understanding of Clinical business processes
  • Experience in process development, mapping, and gap analysis
  • Experience working with vendors and maintaining systems
  • Hands-on experience with SQL, reporting tools (e.g., Spotfire)
  • Knowledge of GxP, CSV, and SDLC and strong understanding of Clinical systems and data
  • Ability to translate business requirements into technical solutions and strong collaboration across business and IT teams
  • Ability to operate in global matrix organizations and strong communication and stakeholder engagement skills
  • Ability to manage change and prioritize based on business value

Your benefits and remuneration:
If the position is filled in the US, the Expected Pay Range is $146,300/year to $234,100/year + benefits, annual bonus & equity (bonus and equity is variable and dependent on company and individual performance). Compensation for the role will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities.
Compensation at other locations may vary significantly.
BioNTech is committed to the wellbeing of our team members and offers a variety of benefits in support of our diverse employee base. We offer competitive remuneration packages which is determined by the specific role, location of employment and also the selected candidate's qualifications and experience.
Note: The availability, eligibility and design of the listed benefits may vary depending on the location. The final requirements for the individual use of our benefits are based on the company's internal policies and applicable law.
How to apply:
Apply now by sending us your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter as well as your contact details via our online form.
Please note:
Only applications sent via our online form shall be considered. By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider 'HireRight'. You will be informed accordingly by your BioNTech-Recruiter.
We are looking forward receiving your application.
Inspired? Become part of #TeamBioNTech.
BioNTech, the story
At BioNTech, we are more than just a biotechnology company - we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting-edge science into survival. Your contributions here have the potential to improve the health of people worldwide, especially by addressing diseases with high medical needs like cancer and various infectious diseases.
Experience a dynamic workplace that embraces diversity in all its forms. We foster innovation, encourage creativity, and develop business strategies driven by our shared passion for advancing medicine.
Working at BioNTech means striving to achieve medical breakthroughs while growing your career in a meaningful way. Apply today and become part of a mission that has the potential to change lives around the world.
BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer. The main thing is that you suit us, and we suit you!
BioNTech - As unique as you
www.biontech.com

Apply