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Union Clinical Research Jobs (NOW HIRING)

Non-Union-NCT Weekend Rotation: None Job Summary: Allina Health is a not-for-profit health system ... Evaluates overall feasibility of the study at the clinical research center and identify budget ...

Clinical Research Coordinator

Sioux Falls, SD · On-site

$24 - $32/hr

Salary Range: $24.00 - $38.50 Union Position: No Department Details This important patient-facing role in clinical research requires strong interpersonal and customer service skills, enthusiasm for ...

Clinical Research Coordinator

Sioux Falls, SD · On-site

$24 - $32/hr

Salary Range: $24.00 - $38.50 Union Position: No Department Details This important patient-facing role in clinical research requires strong interpersonal and customer service skills, enthusiasm for ...

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Union Clinical Research information

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$49K

$107.3K

$189K

How much do union clinical research jobs pay per year?

As of Jun 14, 2026, the average yearly pay for union clinical research in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

Why does union mean?

In the context of a Union Clinical Research job, 'union' refers to a labor union representing employees, which negotiates wages, benefits, and working conditions. Being part of a union can provide job security, collective bargaining power, and access to specific workplace protections. Many clinical research professionals may work in unionized environments, especially in larger organizations or government-funded research settings.

What are the key skills and qualifications needed to thrive in Union Clinical Research, and why are they important?

Success in Union Clinical Research requires a solid background in clinical research methodologies, regulatory compliance, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is highly valuable. Excellent organizational skills, attention to detail, and strong communication abilities help professionals coordinate studies and liaise effectively with union members, clinical staff, and stakeholders. These skills ensure research integrity, participant safety, and regulatory adherence within the unique context of unionized healthcare environments.

What do you mean by union?

In the context of a clinical research job, a union is an organized group of employees that advocates for workers' rights, fair wages, and better working conditions. Union membership can influence employment terms, collective bargaining, and job protections within the workplace.

What is a Union Clinical Research professional?

A Union Clinical Research professional is someone who conducts or oversees clinical trials and research studies within organizations that have unionized workforces, such as hospitals or research institutions with union-represented staff. Their role often includes ensuring that research protocols comply with both scientific standards and union regulations, protecting the rights and interests of unionized participants and employees. They may also facilitate communication between researchers, union representatives, and management to ensure ethical and legal compliance throughout the study process.

What does it mean to be union?

Being union in a clinical research job means being a member of a labor union that advocates for workers' rights, fair wages, and better working conditions. Unionized employees often negotiate collectively through a union representative and may have access to specific benefits and protections mandated by the union contract.

What are some common challenges faced in a Union Clinical Research role and how are they typically addressed?

Professionals in Union Clinical Research often navigate challenges such as coordinating multi-site studies, ensuring adherence to union guidelines, and balancing regulatory compliance with participant safety. Communication across diverse teams—including union representatives, investigators, and sponsors—requires strong organizational and negotiation skills. Many organizations address these challenges through regular team meetings, robust training on union protocols, and established channels for resolving conflicts or clarifying expectations. Proactive collaboration and a thorough understanding of both clinical trial regulations and union contracts are key to success in this role.

Should I join a union at work?

For a clinical research professional, joining a union can provide collective bargaining power, job security, and benefits such as health insurance and grievance procedures. However, union membership may also involve dues and adherence to collective agreements, so it is important to consider the specific union's policies and how they align with your career goals and work environment.
More about Union Clinical Research jobs
What cities are hiring for Union Clinical Research jobs? Cities with the most Union Clinical Research job openings:
What are the most commonly searched types of Clinical Research jobs? The most popular types of Clinical Research jobs are:
What states have the most Union Clinical Research jobs? States with the most job openings for Union Clinical Research jobs include:
Clinical Research Specialist

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago


Allina Health rating

7.7

Company rating: 7.7 out of 10

Based on 259 frontline employees who took The Breakroom Quiz

159th of 872 rated healthcare providers


Job description

Location Address:

2800 10th Ave Receiving Dock Minneapolis, MN 55407-1311

Date Posted:

April 29, 2026

Department:

16000480 AHCI Research

Shift:

Day (United States of America)

Shift Length:

8 hour shift

Hours Per Week:

40

Union Contract:

Non-Union-NCT

Weekend Rotation:

None

Job Summary:

Allina Health is a not-for-profit health system that cares for individuals, families and communities throughout Minnesota and western Wisconsin. If you value putting patients first, consider a career at Allina Health. Our mission is to provide exceptional care as we prevent illness, restore health and provide comfort to all who entrust us with their care. This includes you and your loved ones. We are committed to providing whole person care, investing in your well-being, and enriching your career.

Key Position Details:

  • 1.0 FTE (80 hours per two-week pay period)
  • 8-hour day shift
  • No weekends
  • Will work at Abbott Northwestern Piper Building & West Health Plymouth
  • Oncology experience preferred

Job Description:

Provides multifaceted support to the clinical research department in clinical research department in the clinical trials study activities. Provides patient enrollment and assessments, data management, and study material preparation. Prepares regulatory documents, and coordinates project in accordance with research standard operating procedures, federal and state regulations, Institutional Review Board (IRB) requirements, and International Council on Harmonization Good Clinical Practice guidelines.
Principle Responsibilities

  • Studies Feasibility Activities - in conjunction with research manager and team.
    • Evaluates overall feasibility of the study at the clinical research center and identify budget items needed to perform the study.
    • Evaluates new study protocols: Assesses protocol criteria to determine target enrollment goals related to patient population.
    • Determines and orders special equipment and laboratory needs for new studies.
    • Completes Radiology and Imaging Capabilities Assessment Forms.
  • Studies Start-Up Activities - with research team.
    • Prepares and participates in site qualification visits and site initiation meetings.
    • Collaborates on developing study plan of execution.
    • Assists with recruitment strategies to enhance study enrollment.
    • Creates study-specific tools and materials for protocol implementation.
    • Collaborates with team members in preparing regulatory documents, study materials, laboratory kit supplies, informed consent forms, and recruitment materials.
    • Educates internal and external personnel about studies; provide guidance in implementing study protocols.
  • Studies Management Activities.
    • Screens medical records for potential study participation based on protocol inclusion and exclusion criteria.
    • Conducts and documents the informed consent process with potential research subjects in accordance with SOPs and Institutional Review Board (IRB) requirements.
    • Develops, implements, and evaluates plan of care based upon individual patient and family assessment.
    • Utilizes appropriate procedures, interpreters, forms, etc. for patients with special communication needs.
    • Evaluates study participants and complete all study-related activities including diagnostics, and laboratory procedures.
    • Performs study-related activities and assessments within the scope of training and certification.
    • Manages source documentation and accurately report data in case report forms for each study subject during the study.
    • Ensures all data is entered within sponsor-specified parameters. Resolve queries within the sponsor-specified time periods.
    • Serves as liaison with principal investigator, research staff, clinical care team, and sponsor regarding patient care issues and progress on the study.
    • Communicates about study with the study staff and sponsor regarding patient care issues and study progress.
    • Prepares for study monitoring and audit visits.
    • Oversees study close-out visits.
  • Assists and Collaborates.
    • Assists with lab kit receipt, storage and preparation, ECG monitoring, sending imaging for central review, and preparing and sending lab specimens to central laboratories.
    • Collaborates with members of the research team to ensure the proper collection, processing and shipment of pathology and laboratory specimens.
    • Communicates effectively with member of the research and clinical care teams in person and at meetings.
  • Other duties as assigned.


Required Qualifications

  • Associate's or Vocational degree in a medical or science field
  • 0 to 2 years of experience in clinical research


Preferred Qualifications

  • Bachelor's degree in a medical or science field


Licenses/Certifications

  • Must meet at least ONE of the requirements below
    Current BLS certification from the American Heart Association
    Current BLS certification from the American Red Cross
    Allina in-house BLS training (within 30 days of hire)
  • Certified Clinical Research Coordinator preferred upon hire
  • Certified Clinical Research Professional preferred upon hire
  • Collaborative Institutional Training Initiative (CITI Program) Certification to be completed within (180 days) of hire (offered through Allina Health)


Physical Demands

  • Sedentary:
  • Lifting weight up to 10 lbs. occasionally, negligible weight frequently

Pay Range

Pay Range: $29.31 to $40.17 per hourThe pay described reflects the base hiring pay range. Your starting rate would depend on a variety of factors including, but not limited to, your experience, education, and the union agreement (if applicable). Shift, weekend and/or other differentials may be available to increase your pay rate for certain shifts or work.

Benefit Summary

Allina Health believes the best way to provide safe and compassionate care for our patients is by nurturing the passion of those who care for them. That's why we devote extraordinary resources to help you grow and thrive - not only as a professional but also as a whole person. When you join our team, you have access to a wealth of valuable employee benefits that support the total well-being - mind, body, spirit and community - of you and your family members.

Allina Health is all in on your well-being. Because well-being means something different to everyone, our award-winning program provides you with the resources you need to help you navigate your personal journey. This includes well-being dollars, dedicated well-being navigators, and many programs, activities, articles, videos, personal coaching and tools to support you on your journey.

In addition, Allina Health offers employee resources groups (ERGs) -- voluntary, employee-led groups that serve as a resource for members and organizations by fostering a diverse, inclusive workplace aligned with the organization's mission, values, goals, business practices, and objectives. Allina Health also engages employees in various community involvement and volunteering events.

Benefits include:

  • Medical/Dental

  • PTO/Time Away

  • Retirement Savings Plans

  • Life Insurance

  • Short-term/Long-term Disability

  • Voluntary Benefits (vision, legal, critical illness)

  • Tuition Reimbursement or Continuing Medical Education as applicable

  • Student Loan Support Benefits to navigate the Federal Public Service Loan Forgiveness Program

  • Allina Health is a 501(c)(3) eligible employer

*Benefit eligibility/offerings are determined by FTE and if you are represented by a union.


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