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Socra Jobs in Minnesota (NOW HIRING)

IT Project Manager

Bemidji, MN · On-site

$96K - $113K/yr

Additionally, based on department needs and supporting areas, certification through Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) may be ...

Certification as a Research Professional by Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP). Work habits include organization, coordination of ...

ACRP or SOCRA certification. BENEFITS * NMDP offers regular, full-time employees medical, dental, vision, life and disability, accident/critical illness/hospital, well-being, legal, identity theft ...

Professional certification in Clinical Research (e.g., SoCRA, ACRP). Danaher Diagnostics, a Danaher company, offers a broad array of comprehensive, competitive benefit programs that add value to our ...

Principal Clinical Scientist

Chaska, MN · On-site

$120K - $165K/yr

Professional certification in Clinical Research (e.g., SoCRA, ACRP). Danaher Diagnostics, a Danaher company, offers a broad array of comprehensive, competitive benefit programs that add value to our ...

Professional certification in Clinical Research (e.g., SoCRA, ACRP). Beckman Coulter Diagnostics, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that ...

Professional certification in Clinical Research (e.g., SoCRA, ACRP). Beckman Coulter Diagnostics, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that ...

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Socra information

See Minnesota salary details

$11

$40

$68

How much do socra jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for socra in Minnesota is $40.28, according to ZipRecruiter salary data. Most workers in this role earn between $28.27 and $51.54 per hour, depending on experience, location, and employer.

What is a Socra?

A Socra job typically refers to a role in clinical research, often associated with the certification provided by the Society of Clinical Research Associates (SoCRA). Professionals in this field are responsible for ensuring clinical trials comply with regulatory requirements, ethical guidelines, and study protocols. They may work as Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), or other related positions. Their duties include monitoring clinical trials, maintaining accurate documentation, and safeguarding patient safety throughout the study process. Obtaining SoCRA certification can enhance credibility and career opportunities in the clinical research industry.

What are SOC RAs (Security Operations Center Research Analysts)?

SOC RAs, or Security Operations Center Research Analysts, are professionals who monitor, detect, investigate, and respond to cybersecurity threats within an organization. They analyze security alerts, assess vulnerabilities, and work closely with other IT and security staff to ensure incidents are managed effectively. Their role is critical in maintaining the organization’s security posture and protecting sensitive data from potential breaches. SOC RAs typically use various security tools and techniques to identify and mitigate risks in real-time.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate (SOCRA), and why are they important?

To thrive as a Clinical Research Associate (SOCRA), you need a solid understanding of clinical trial processes, regulatory guidelines, and a relevant life sciences degree or certification such as SOCRA's CCRP. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and Good Clinical Practice (GCP) guidelines is typically required. Strong attention to detail, organizational skills, and effective communication are crucial soft skills for managing study protocols and collaborating with research teams. These competencies ensure the integrity of clinical trials, regulatory compliance, and the successful advancement of medical research.

What are some common challenges faced by Socra (Study Coordinator) professionals when managing multiple clinical trials simultaneously?

Socra professionals, or Study Coordinators, often manage several clinical trials at once, which can present challenges in prioritizing tasks, maintaining regulatory compliance, and ensuring accurate documentation across studies. Balancing communication with different research teams, investigators, and sponsors while meeting tight deadlines requires strong organizational and multitasking skills. Staying updated with protocol amendments and managing participant recruitment and retention can also be demanding aspects of the role.

What is the difference between Socra vs Data Analyst?

AspectSocraData Analyst
Required CredentialsTypically requires a degree in social sciences, research methods, or related fields; certifications in data collection or analysis are a plusRequires a degree in statistics, mathematics, or related fields; certifications like CAP or Microsoft Data Analyst are common
Work EnvironmentPrimarily fieldwork, interviews, and data collection in social or community settingsOffice-based, analyzing data sets, creating reports, and visualizations
Employer & Industry UsageUsed by research organizations, NGOs, and government agencies for social researchUsed across industries like finance, marketing, healthcare, and technology for data-driven decision making

While both Socra and Data Analyst roles involve data handling, Socra focuses more on social research and fieldwork, whereas Data Analysts primarily analyze digital data in office settings. The roles share similar educational backgrounds and certifications but differ in work environment and industry application.

What job categories do people searching Socra jobs in Minnesota look for?

The top searched job categories for Socra jobs in Minnesota are:

Infographic showing various Socra job openings in Minnesota as of August 2026, with employment types broken down into 58% Full Time, and 42% Part Time. Highlights an 100% In-person job distribution, with an average salary of $83,781 per year, or $40.3 per hour.

Clinical Research Coordinator, RP3

University of Minnesota

Minneapolis, MN

$41.82 - $44.72/hr

Full-time

Medical, Dental, Life, Retirement

Posted 15 days ago


Job description

About the Job
 

Position Summary: This position will serve as a lead Clinical Research Coordinator for a Sleep Neurologist who studies the relationship between sleep and Alzheimer's disease pathology. This position requires an experienced Clinical Research coordinator who will coordinate clinical research trials in treatment of sleep disorders including diagnostic and therapeutic services, under PI supervision. The person who takes this position may be responsible for multiple research studies simultaneously, acting as a liaison with the PI, IRB, sponsoring agency, community and the study participants. The role will be responsible for managing and recording all phases of study protocol as required by GCP and sponsoring agencies to ensure compliance. This role will be in person 2-3 days per week at the University of MN, Twin Cities campus and at clinical sites within the Twin City Metro area. Visa sponsorship and/ or relocation assistance not available for this position. 
Work Schedule: Hybrid (in-person 2-3 days a week), M-F, 7:30am - 4pm
Duties/Responsibilities: 
50% - Research Study Visits:

  • Independently identify, recruit, screen, and consent participants for sleep related research.
  • Work with PI in determining participant eligibility based on diagnostic criteria and/or observations/analysis in participant interviews.
  • Serve as research coordinator to lead clinical research study visits with participants in-person and remotely.
  • Manage data entry from research visits in a timely and attentive to detail method.
  • Ensure a safe physical environment for research participation when collecting sleep research which utilizes data using polysomnography, home sleep testing, single-channel EEG devices and actigraphy.
  • Manage HIPAA compliant secure data storage of all study materials.
  • Independently explain diagnostic procedures and study procedures and plans to participants.
  • Independently administers/scores tests, route all lab and clinical in a timely manner to PI for evaluation.
  • Lead and develop data collection methods and CRFs for study data.
  • Independently perform assessments to ensure they are completed in a timely manner.

25% - Scheduling and Communication:

  • Follow protocol to schedule and facilitate the patients timely completion adhering to protocol requirements.
  • Manage communications with PI, Sponsor, IRB, other regulatory groups, and participants as needed to ensure safety, adherence to protocol, AEs, SAES and understanding of studies.

20% - Regulatory, Compliance and Sponsor liaison:

  • Comply with protocol guidelines, Good Clinical Practices (GCP), all applicable University guidelines, Standard operation procedures (SOPs), laws, and requirements of regulatory agencies.
  • Coordinate site visits with industry sponsors; serve as a liaison with funding or sponsoring agencies.
  • Manage IRB submissions, continuing annual reviews and Serious Adverse Event reporting (SAE); recommends protocol correction action plans as appropriate.

3% - Research protocol development:

  • Works with principal investigator and collaborates with other investigators within the university to develop research studies as needed.

2% - Other duties:

  • Performs other duties in addition to the work described above.
     
Qualifications
 

All required qualifications must be included in the application materials

Required Qualifications:

  • BA/BS degree in a health-related field (Pre-Med, Psychology, Neuroscience, Nursing, etc.) plus at least four (4) years of work experience, or advanced degree plus 2 years of experience in research setting, or a combination of related education and work experience to equal eight (8) years of relevant experience.
  • Experience with recruiting study participants and running research participant visits.
  • Ability to collaborate with clinical sites to conduct research visits.
  • Experience or Interest in learning how to complete remote participant visits.
  • Experience problem solving and prioritizing essential clinical research components of a research participant visit.
  • Organized with excellent attention to detail.
  • Excellent verbal and written communication skills.
  • Must demonstrate independence and interpersonal skills.
  • Must comply with applicable laws, regulations, guidelines and standards regarding patient safety and infection control issues.
  • Willing to work on site (Twin Cities) at least 2-3 days per week.

Preferred Qualifications: 

  • Familiarity with regulatory research processes within the context of participant-facing research visits (e.g. consenting participants for research, HIPAA form completion).
  • Enthusiasm for medical research studies and being a part of the decision-making process for research.
  • Certified clinical research professional (e.g., SoCRA or ACRP). We would also support a research professional who wishes to get their SoCRA or ACRP certification.
About the Department
 

To learn more about the Department of Neurology, please visit https://med.umn.edu/neurology. 

Pay and Benefits
 

Pay Range: $41.82/hr - $44.72/hr; depending on education/qualifications/experience

Time Appointment: 100% Appointment

Position Type: Civil-Service & Non-Faculty Labor Represented Staff

Please visit the Office of Human Resources website for more information regarding benefit eligibility.

The University offers a comprehensive benefits package that includes:

  • Competitive wages, paid holidays, and generous time off
  • Continuous learning opportunities through professional training and degree-seeking programs supported by the Regents Tuition Benefit Program
  • Low-cost medical, dental, and pharmacy plans
  • Healthcare and dependent care flexible spending accounts
  • University HSA contributions
  • Disability and employer-paid life insurance
  • Employee wellbeing program
  • Excellent retirement plans with employer contribution
  • Public Service Loan Forgiveness (PSLF) opportunity
  • Financial counseling services 
  • Employee Assistance Program with eight sessions of counseling at no cost
  • Employee Transit Pass with free or reduced rates in the Twin Cities metro area

While our salary ranges provide a framework, it is important to note that most of the time, the initial pay may not reach the maximum of the range. This approach ensures that compensation reflects the value and unique contributions of each candidate while maintaining equity within our organization. As part of our commitment to fair and equitable compensation, please be aware that the salary offered to incoming candidates will be based on their individual credentials and experience.

How To Apply
 

Applications must be submitted online.  To be considered for this position, please click the Apply button and follow the instructions.  You will be given the opportunity to complete an online application for the position and attach a cover letter and resume.

Additional documents may be attached after application by accessing your "My Job Applications" page and uploading documents in the "My Cover Letters and Attachments" section.

To request an accommodation during the application process, please e-mail employ@umn.edu or call (612) 624-8647.

Diversity
 

The University recognizes and values the importance of diversity and inclusion in enriching the employment experience of its employees and in supporting the academic mission.  The University is committed to attracting and retaining employees with varying identities and backgrounds.

The University of Minnesota provides equal access to and opportunity in its programs, facilities, and employment without regard to race, color, creed, religion, national origin, gender, age, marital status, disability, public assistance status, veteran status, sexual orientation, gender identity, or gender expression.  To learn more about diversity at the U:  http://diversity.umn.edu

Employment Requirements
 

Any offer of employment is contingent upon the successful completion of a background check. Our presumption is that prospective employees are eligible to work here. Criminal convictions do not automatically disqualify finalists from employment.

About University of Minnesota
 

The University of Minnesota, Twin Cities (UMTC)

The University of Minnesota, Twin Cities (UMTC), is among the largest public research universities in the country, offering undergraduate, graduate, and professional students a multitude of opportunities for study and research. Located at the heart of one of the nation's most vibrant, diverse metropolitan communities, students on the campuses in Minneapolis and St. Paul benefit from extensive partnerships with world-renowned health centers, international corporations, government agencies, and arts, nonprofit, and public service organizations.

At the University of Minnesota, we are proud to be recognized by Forbes as a Best Employer for Company Culture (2026), Best Employer for Women (2023, 2025, 2026), and Best Employer by State (2022-2026). In 2026, we also received Culture Excellence & Industry Awards recognition for employee appreciation and work-life flexibility.