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Clinical Database Programmer Jobs in Minnesota (NOW HIRING)

SV Tech Systems Inc

SQL Developer

Moundsview, MN · Remote

$48 - $65.75/hr

Work as a Database Administrator for a leading Medical Device company to alleviate pain, restore ... You will support a Web Based Remote Patient Management System used by our clinicians on behalf of ...

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Clinical Database Programmer information

See Minnesota salary details

$68.1K

$116.5K

$207.6K

How much do clinical database programmer jobs pay per year?

As of May 29, 2026, the average yearly pay for clinical database programmer in Minnesota is $116,513.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,400.00 and $176,300.00 per year, depending on experience, location, and employer.

What is a Clinical Database Programmer job?

A Clinical Database Programmer is responsible for designing, developing, and maintaining databases used in clinical trials. They ensure that data is collected, stored, and managed efficiently while complying with regulatory standards such as CDISC and FDA guidelines. Their role involves creating database structures, writing validation checks, and supporting data analysis to ensure accurate and reliable clinical trial results. They often work with clinical data managers, biostatisticians, and regulatory teams.

What are the key skills and qualifications needed to thrive in the Clinical Database Programmer position, and why are they important?

To excel as a Clinical Database Programmer, you need a bachelor's degree in computer science or a related field, experience in database design, and a strong understanding of clinical data standards. Proficiency in database management systems (such as Oracle or SQL), knowledge of electronic data capture (EDC) tools like Medidata Rave, and familiarity with programming languages like SAS or SQL are commonly required, along with certifications such as CDISC or Medidata Solutions. Attention to detail, problem-solving ability, and strong communication skills are valuable soft skills for this role. Mastering these competencies is vital for ensuring high-quality, regulatory-compliant clinical trial data and effective collaboration within multidisciplinary research teams.

What are common responsibilities and team interactions for a Clinical Database Programmer in a typical workweek?

As a Clinical Database Programmer, your primary responsibilities usually include designing, building, and validating clinical trial databases, ensuring data is collected and managed in compliance with industry standards and regulatory requirements. You will frequently collaborate with clinical data managers, biostatisticians, and study coordinators to define data collection requirements and resolve data discrepancies. Team meetings and cross-functional communication are integral parts of the role, as you work together to maintain database integrity throughout the study lifecycle. This collaborative environment provides valuable experience in both technical problem-solving and teamwork, often paving the way for advancement into senior programming or data management positions.
More about Clinical Database Programmer jobs
What are the most commonly searched types of Clinical Database Programmer jobs in Minnesota? The most popular types of Clinical Database Programmer jobs in Minnesota are:
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What job categories do people searching Clinical Database Programmer jobs in Minnesota look for? The top searched job categories for Clinical Database Programmer jobs in Minnesota are:
What are popular job titles related to Clinical Database Programmer jobs in MN? For Clinical Database Programmer jobs in MN, the most frequently searched job titles are:
Clinical Database Programmer jobs near you
Infographic showing various Clinical Database Programmer job openings in Minnesota as of May 2026, with employment types broken down into 3% As Needed, 90% Full Time, and 7% Contract. Highlights an 71% Physical, 6% Hybrid, and 23% Remote job distribution, with an average salary of $116,513 per year, or $56 per hour.
Clinical Trial Specialist

Clinical Trial Specialist

4C Medical Technologies

Maple Grove, MN • On-site

$75K - $100K/yr

Full-time

Posted 10 days ago

Job description

Job Type
Full-time
Description
JOB SUMMARY:
Under general supervision, develops, coordinates, and administers the logistical aspects of clinical trials according to good clinical practice (GCP), good documentation practices (GDP) and standard operating procedures (SOP). Acts as a pivotal point of contact and communication between department staff, clinical sites, as well as vendors.
KEY RESPONSIBILITIES :
1. Oversee and manage operational aspects of clinical trials in conjunction with project teams and in accordance with SOPs, GCP, GDP and specific country regulations, and may prepare clinical trial budgets.
2. Collaborate and partner with a cross-functional team which includes clinical field, site managers, monitors, safety, and others.
3. Build and maintain optimal relationships and effective collaborations with various internal and external parties.
4. Develop, test, and implement clinical tools to provide relevant information for clinical studies management.
5. Manage clinical study site information and documentation.
a. Request, track, review and assure receipt of proper study documentation (IRB approval letters, Signature Pages, Informed Consent materials, signed Clinical Study Agreements, Confidentiality Agreements, etc.).
b. Obtain, review, and file site personnel documentation to ensure site compliance.
c. Develop and distribute clinical study documents (Protocol, Case Report Forms, Informed Consent, Agreements, etc.).
6. Routinely correspond with clinical study sites.
a. Provide timely support as subjects go through the screening process.
b. Promptly answers sites' questions and requests with accuracy.
c. Generate and submit memos and study documents (protocol amendments, newsletters, brochures, etc.) to clinical study sites.
d. Generate, review, and respond to queries the electronic data capture (EDC).
7. Coordinate all information regarding adverse events and ensure all information is received by the internal team and clinical study sites.
8. Maintain accurate records and files of study patient data. Coordinate accurate completion of Case Report Forms in EDC by timely reviewing them and corresponding with sites to update data and/or creating corrective action plans.
9. Coordinate on-site and off-site Investigator, Study Coordinator and Technologist training meetings and conference calls.
10. Provide support to monitoring staff by creating monitoring visit prep packages, answering monitors' questions during visits, and reviewing monitoring visit reports.
11. Order, assemble, and maintain supplies of study materials and equipment (handbooks, Case Report Form books, IDE copies, medical equipment, etc.).
12. Other duties, as assigned by supervisor and/or clinical research project managers.
Requirements
EDUCATION :
Bachelor's degree in engineering, biology, physical sciences, nursing or another related field.
PREFERRED EXPERIENCE :
One plus years of experience in clinical/medical affairs in the medical device industry.
KNOWLEDGE, SKILLS AND ABILITIES:
  • Knowledge of medical terminology and anatomy.
  • Knowledge of FDA guidelines and regulations governing conduct of clinical trials.
  • Detailed knowledge of the documents required for a Regulatory Binder (IRB approvals, Investigator Agreements, CVs, MLs).
  • Strong organizational skills and detail orientation required.
  • Interpersonal and communication skills necessary to interact with study site personnel and physicians.
  • Analytical skills to determine clinical requirements and evaluate software solutions.
  • Intermediate skills in Microsoft Office, Word, and Power Point.
  • Advanced skills in Excel, Access, and clinical database software.
  • Ability to handle multiple priorities in a fast-paced environment.
  • Ability to make independent judgments.
  • Ability to travel as needed up to 20%.

Salary Description
$75,000 to $100,000

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