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Clinical Research Relocation Jobs in Michigan (NOW HIRING)

This is a rare opportunity to shape your own clinical and research focus, step into leadership, and ... Relocation assistance Candidate Requirements * MD or DO degree required * Board eligible or board ...

This is a rare opportunity to shape your own clinical and research focus, step into leadership, and ... Relocation assistance Candidate Requirements * MD or DO degree required * Board eligible or board ...

This is a rare opportunity to shape your own clinical and research focus, step into leadership, and ... Relocation assistance Candidate Requirements * MD or DO degree required * Board eligible or board ...

Clinical Research Institute support: infrastructure and dedicated personnel * Strong junior faculty ... Relocation assistance Shift & Schedule * Protected research/administrative time commensurate with ...

Clinical Research Institute support: infrastructure and dedicated personnel * Strong junior faculty ... Relocation assistance Candidate Requirements * MD, DO, or MD/PhD required * Board certified or ...

Clinical Research Institute support: infrastructure and dedicated personnel * Strong junior faculty ... Relocation assistance Candidate Requirements * MD, DO, or MD/PhD required * Board certified or ...

Clinical Research Institute support: infrastructure and dedicated personnel * Strong junior faculty ... Relocation assistance Candidate Requirements * MD, DO, or MD/PhD required * Board certified or ...

This role offers a unique opportunity to shape clinical and research focus within one of Michigan ... Relocation assistance Benefits * Health, dental, and life insurance * 401(k) with employer matching ...

Clinical Research Institute support: infrastructure and dedicated personnel * Strong junior faculty ... Relocation assistance Candidate Requirements * MD, DO, or MD/PhD required * Board certified or ...

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Clinical Research Relocation information

What are some common challenges clinical research professionals face when relocating for a new position, and how can they prepare?

Relocating for a clinical research role often involves adjusting to new regulatory environments, learning institutional protocols, and building relationships with unfamiliar site teams. It can be challenging to quickly integrate into established workflows and local cultures, especially when overseeing multiple research sites or adapting to varying patient populations. To prepare, candidates should research the local regulatory landscape, reach out to future colleagues ahead of time, and seek support from their employer's HR or relocation services to ensure a smoother transition.

What is the difference between Clinical Research Relocation vs Clinical Research Coordinator?

AspectClinical Research RelocationClinical Research Coordinator
CredentialsTypically requires experience in clinical research, sometimes certifications like CCRPRequires knowledge of clinical trial protocols, often a degree in health sciences or related field
Work EnvironmentInvolves managing logistics of relocating research staff or sites, often travel and coordinationWorks directly with patients, investigators, and study teams at research sites
Employer & Industry UsageUsed by research organizations, pharmaceutical companies, and CROs for site or staff movementCommonly employed at hospitals, research centers, and clinical trial sites

Clinical Research Relocation focuses on managing the logistics of moving research staff or sites, while Clinical Research Coordinators handle day-to-day trial operations at research sites. Both roles require knowledge of clinical research processes but serve different functions within the industry.

What is clinical research relocation?

Clinical research relocation refers to the process of moving clinical research operations, staff, or study participants from one location to another. This may occur due to regulatory requirements, expansion, or to access better facilities and patient populations. Relocation requires careful planning to ensure compliance with protocols, maintain data integrity, and minimize disruption to ongoing studies. It also often involves logistical coordination, regulatory approvals, and communication with stakeholders. In some cases, relocation support is provided to research staff or participants to facilitate the transition.

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

To thrive in Clinical Research Relocation, you need a background in clinical research, project management, and regulatory compliance, often supported by a relevant life sciences degree. Familiarity with clinical trial management systems (CTMS), standard operating procedures (SOPs), and knowledge of Good Clinical Practice (GCP) guidelines is essential. Strong organizational skills, adaptability, and effective communication are critical for coordinating logistics and ensuring smooth transitions for studies, staff, or participants. These skills ensure regulatory adherence, minimize disruptions, and support the seamless execution of clinical research activities during relocation processes.
What are popular job titles related to Clinical Research Relocation jobs in Michigan? For Clinical Research Relocation jobs in Michigan, the most frequently searched job titles are:
What cities in Michigan are hiring for Clinical Research Relocation jobs? Cities in Michigan with the most Clinical Research Relocation job openings:
Infographic showing various Clinical Research Relocation job openings in Michigan as of July 2026, with employment types broken down into 93% Full Time, and 7% Contract. Highlights an 86% In-person, 7% Hybrid, and 7% Remote job distribution.
Clinical Research Coordinator

Clinical Research Coordinator

Hypertension Nephrology Associates

Livonia, MI • On-site

$48K/yr

Full-time

Medical, Dental, Retirement, PTO

Posted 18 days ago


Job description


Position Overview

We are seeking a detail-oriented and patient-focused Clinical Research Coordinator to support our clinical research program. This role combines clinical care responsibilities with research coordination and administrative support.


The ideal candidate will bring experience in clinical trials, strong organizational skills, and a foundational understanding of study protocols and GCP guidelines. This role is well-suited for a Medical Assistant with research experience who is looking to further develop their skills in a clinical trials setting.


RESPONSIBILITIES

  • Assist in the coordination and execution of clinical trial activities in accordance with study protocols and ICH-GCP guidelines
  • Prepare study materials, equipment, and documentation for patient visits
  • Conduct protocol-specific procedures, interviews, and data collection
  • Maintain accurate and complete study documentation, including regulatory binders and source documents
  • Perform data entry and resolve study-related data queries
  • Verify patient records post-visit to ensure completeness and protocol compliance
  • Support subject recruitment, visit tracking, scheduling, and study-related financial tracking
  • Assist with the development and maintenance of source documents
  • Maintain organized and audit-ready study files (paper and electronic)
  • Provide administrative support across active clinical trials
  • Assist providers with patient care workflows during clinic visits
  • Collect patient medical histories and document clinical information
  • Perform vital signs, phlebotomy, and basic clinical procedures
  • Support medication reconciliation and communicate updates to providers
  • Maintain accurate documentation in the Electronic Medical Record (EMR) system
  • Educate patients on treatment plans, study participation, and follow-up care
  • Assist with scheduling, patient communication, and follow-up coordination
  • Ensure a clean, organized, and well-functioning clinical environment


QUALIFICATIONS

    • Previous administration experience in a private practice or clinical setting
    • IT Proficiency (Microsoft Office package)
    • Good verbal and written communication skills
    • Strong attention to detail and organizational skills
    • Proficiency with electronic medical records (EMR) and electronic data capture (EDC) systems
    • Clinical trials and/or medical practice experience
    • Experience managing essential documents for clinical trials according to ICH GCP
    • Experience using electronic data capture systems
    • Experience with phlebotomy, EKG, and Vital signs collection
    • Associate's degree in a science, technical, health-related field, or another applicable discipline (not required in lieu of experiences and certifications


BENEFITS

    • Completion of Good Clinical Practice (GCP) training
    • CME hours
    • 401(k)
    • Dental insurance
    • Health insurance
    • Paid time off


LOCAL CANDIDATES PREFERRED / NO RELOCATION ASSISTANCE