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Clinical Trial Transparency Associate Jobs in Michigan

START Center for Cancer Research

Patient Navigator

Grand Rapids, MI · On-site

$19.25 - $26.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Associates degree in healthcare or related field. * Clinical trial experience. * Strong organizational and communication skills. Best-in-Class Benefits and Perks We value the time, talent, and ...

START Center for Cancer Research

Patient Navigator

Grand Rapids, MI · On-site

$19.25 - $26.25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Associate's degree in healthcare or related field. * Clinical trial experience. * Strong organizational and communication skills. Best-in-Class Benefits and Perks We value the time, talent, and ...

Microbiologics

R&D Associate - Med Tech

Portage, MI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Description R&D Associate - Med Tech At Microbiologics, our impact goes far beyond the lab. As a ... You will contribute to meaningful anti-infective research, support clinical trial laboratory ...

Microbiologics, Inc.

R&D Associate - Med Tech

Portage, MI · On-site

$55K - $60K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Description R&D Associate - Med Tech At Microbiologics, our impact goes far beyond the lab. As a ... You will contribute to meaningful anti-infective research, support clinical trial laboratory ...

BAMF Health

Clinical Research Nurse- Start Up

Grand Rapids, MI · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Clinical Research Nurse - Start Up plays a vital role in the early phases of clinical trial ... Associate's degree in nursing required * 2 years of RN experience in a healthcare setting required ...

New

Becton, Dickinson and Company

  • Medical

  • Life

Strong understanding of clinical trial operations, monitoring practices, investigational product ... associates through our comprehensive Total Rewards program. We are committed to attracting and ...

New

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Showing results 21-40

All JobsClinical Trial Transparency Associate JobsClinical Trial Transparency Associate Jobs in Michigan

Clinical Trial Transparency Associate information

See Michigan salary details

$15

$34

$61

How much do clinical trial transparency associate jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for clinical trial transparency associate in Michigan is $34.85, according to ZipRecruiter salary data. Most workers in this role earn between $28.08 and $38.37 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical trial transparency associate?

To thrive as a Clinical Trial Transparency Associate, you need a solid understanding of clinical research processes, regulatory requirements (such as FDA, EMA, and ICMJE), and a relevant life sciences degree. Familiarity with clinical trial registries (e.g., ClinicalTrials.gov), disclosure platforms, and data anonymization tools is typically required. Exceptional attention to detail, organizational skills, and the ability to communicate complex information clearly are vital soft skills. These competencies ensure accurate and compliant disclosure of clinical trial data, supporting regulatory obligations and public trust in research.

What is a clinical trial transparency associate?

Clinical Trial Transparency Associates are professionals responsible for ensuring that information about clinical trials is accurately disclosed and publicly available in compliance with regulatory requirements. Their work includes preparing and submitting trial data to clinical trial registries, redacting sensitive information, and supporting the publication of trial results. They help organizations maintain transparency with stakeholders, including patients, regulators, and the scientific community. This role is essential to promote trust, ethical standards, and data sharing in medical research.

What is the difference between Clinical Trial Transparency Associate vs Clinical Data Coordinator?

AspectClinical Trial Transparency AssociateClinical Data Coordinator
Required CredentialsBachelor's degree, knowledge of clinical trial regulationsBachelor's degree, understanding of clinical data management
Work EnvironmentPharmaceutical or biotech companies, CROsResearch sites, hospitals, clinical research organizations
Employer & Industry UsageUsed in clinical trial disclosure and transparency effortsUsed in managing and coordinating clinical data collection
Common Search & Comparison IntentUnderstanding roles in clinical trial transparencyDistinguishing data management roles in clinical research

The Clinical Trial Transparency Associate focuses on ensuring clinical trial data is publicly disclosed in compliance with regulations, while the Clinical Data Coordinator manages and organizes clinical data collection and entry. Both roles require a background in clinical research but serve different functions within the clinical trial process.

What are some typical challenges faced by a clinical trial transparency associate when managing trial disclosure requirements?

Clinical Trial Transparency Associates often encounter challenges in navigating diverse regulatory requirements across different countries, as disclosure rules can vary significantly by region and sponsor. Coordinating with multiple stakeholders—from clinical teams to legal and regulatory departments—can also be complex, especially when ensuring timely and accurate data submissions. Staying updated on evolving transparency guidelines and managing large volumes of documentation are key aspects of the role. Proactive communication, strong organizational skills, and attention to detail are essential to successfully overcoming these challenges.
What are the most commonly searched types of Clinical Trial Transparency jobs in Michigan? The most popular types of Clinical Trial Transparency jobs in Michigan are:
What are popular job titles related to Clinical Trial Transparency Associate jobs in Michigan? For Clinical Trial Transparency Associate jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Transparency Associate jobs in Michigan look for? The top searched job categories for Clinical Trial Transparency Associate jobs in Michigan are:
What cities in Michigan are hiring for Clinical Trial Transparency Associate jobs? Cities in Michigan with the most Clinical Trial Transparency Associate job openings:
Clinical Trial Transparency Associate jobs near you

Clinical Research Coordinator

Hypertension Nephrology Associates

Livonia, MI • On-site

Full-time

Medical, Dental, Retirement, PTO

Re-posted 6 days ago

Job description

Salary: $48,000 $60,000 annually


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