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Clinical Trials Associate Jobs in Michigan (NOW HIRING)

Sparrow Health System

RN CLINICAL TRIALS

Lansing, MI · On-site

Associates may be asked to perform additional duties as assigned by their leader. Leadership has ... and clinical trials. * Experience with computer data entry and database management * Excellence ...

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Clinical Trials Associate information

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$15

$34

$61

How much do clinical trials associate jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical trials 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 is a clinical trials associate?

Clinical Trials Associates (CTAs) are professionals who support the planning, coordination, and administration of clinical research studies, often working under the supervision of Clinical Research Coordinators or Managers. Their responsibilities typically include maintaining study documentation, ensuring regulatory compliance, assisting with data collection, and communicating with study sites. CTAs play a critical role in ensuring that clinical trials run smoothly and adhere to strict protocols and guidelines. Their work helps bring new medical treatments and therapies to market safely and efficiently.

What are the key skills and qualifications needed to thrive as a clinical trials associate, and why are they important?

To thrive as a Clinical Trials Associate, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, typically supported by a life sciences degree. Familiarity with systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and knowledge of Good Clinical Practice (GCP) guidelines or related certifications is important. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating study activities and collaborating with diverse teams. These skills ensure accurate trial execution, regulatory adherence, and successful study outcomes.

What are some common challenges faced by clinical trials associates, and how can they be managed effectively?

Clinical Trials Associates often face challenges such as coordinating with multiple stakeholders, managing tight deadlines, and ensuring strict compliance with regulatory guidelines. Balancing administrative tasks with participant communication requires strong organizational skills and attention to detail. Staying proactive in communication, utilizing project management tools, and seeking guidance from senior team members can help manage these challenges effectively while fostering a collaborative team environment.

What is the difference between Clinical Trials Associate vs Clinical Research Coordinator?

AspectClinical Trials AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRA are commonBachelor's degree in health sciences or related field; certifications like CCRP are advantageous
Work EnvironmentTypically works in clinical trial sites, pharmaceutical companies, or CROsWorks directly at clinical sites, hospitals, or research centers
Job FocusSupports trial setup, data entry, and regulatory complianceManages patient recruitment, scheduling, and data collection

While both roles support clinical research, Clinical Trials Associates primarily focus on trial logistics and compliance, whereas Clinical Research Coordinators handle patient interactions and site management. Both positions require similar educational backgrounds and certifications, often working in the same environments, but their daily responsibilities differ.

Is a clinical trials associate a good career?

A clinical trials associate is a valuable role in the healthcare and pharmaceutical industries, responsible for coordinating and monitoring clinical trial activities. It offers opportunities for career growth, requires attention to detail, and often involves working with regulatory guidelines and data management tools. The role can be stable and rewarding for those interested in medical research and patient safety.

What do I need to be a clinical trials associate?

To become a clinical trials associate, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with clinical trial management systems or regulatory documentation. Certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.

What are the most commonly searched types of Clinical Trials jobs in Michigan?

The most popular types of Clinical Trials jobs in Michigan are:

What cities in Michigan are hiring for Clinical Trials Associate jobs?

Cities in Michigan with the most Clinical Trials Associate job openings:

Clinical Trials Associate jobs near you
Infographic showing various Clinical Trials Associate job openings in Michigan as of August 2026, with employment types broken down into 2% As Needed, 70% Full Time, 22% Part Time, and 6% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $72,490 per year, or $34.9 per hour.

RN CLINICAL TRIALS

Sparrow Health System

Lansing, MI • On-site

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description


Job Opportunity
Job ID:55469 Positions Location: Lansing, MI Job Description General Purpose of Job: To coordinate
Description:

Positions Location: Lansing, MI

Job Description

General Purpose of Job:

To coordinate and facilitate Clinical Trials activities for the Cancer Center and its Investigators. Provides nursing care in accordance with physicians' orders and applicable policies and procedures. Performs related work as required.

Essential Duties:

This job description is intended to cover the minimum essential duties assigned on a regular basis. Associates may be asked to perform additional duties as assigned by their leader. Leadership has the right to alter or modify the duties of the position.

  • Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on protocol. Manage assigned protocols and activities.
  • Knows the EPIC EMR system to coordinate patient care in compliance with protocol requirements.
  • May disburse investigational drug and provide patient teaching regarding administration. Maintains investigational drug accountability.
  • In collaboration with the physician, reviews patients for changes in condition, nursing assessments of adverse events in patients, concomitant medication use, protocol compliance, response to study drug, and thoroughly documents all findings in EPIC.
  • Research and prepare chemotherapy orders in BEACON for treatments for physician signature. Familiar with beacon orders.
  • Responsible for accurate and timely data collection, documentation, entry, and reporting. Schedules and participates in monitoring and auditing activities.
  • Maintains regulatory documents in accordance with SOP and applicable regulations. - Participates in required training and education programs.
  • May oversee the preparation of orders by physicians to assure that protocol compliance is maintained.
  • Communicates with physician regarding study requirements, need for dose modification, and adverse event reporting.
  • Provides a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards as issued through OSHA.
  • Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
  • Managing all disease groups and cancer diagnoses

Job Requirements
General Requirements
REQUIRED: * Current Michigan license to practice as a Registered Nurse. * BLS or ACLS certification within 60 days of hire. * Oncology Nursing Certification (OCN) within 3 years of hire. Prior to obtaining certification, must maintain 12 oncology specific CEU's per year.
Work Experience
REQUIRED: * Clinical knowledge and critical thinking skills necessary to deliver quality patient care. PREFERRED: * Minimum 2 years of Clinical Oncology experience and/or Research experience. * 2 years of RN experience. * Experience as a Clinic or office nurse in oncology practice. * Experience with oncology patient care including follow up of patient's chemo orders, tests, releasing chemotherapy, Lab tests and ECG reports to ensure compliance with protocols.
Education
REQUIRED: * Graduate from an accredited program for Nursing. * BSN
Specialized Knowledge and Skills
REQUIRED: * Proficient with EPIC and BEACON EMR system. * Knowledge of medical terminology, nursing assessment, anatomy and physiology, clinical medicine, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology, and clinical trials. * Experience with computer data entry and database management * Excellence written and oral communication skills * Excellent organizational skills * Attention to details and accuracy * Ability to read, analyze and interpret technical procedures, such as: protocols, informed consent documents and regulatory documents. * Ability to work independently, organize, prioritize, and follow through with results * Ability to solve practical problems and implement solutions * Ability to conceptualize GCP concepts * Attend audits offsite and on site with monitors. * Ability to adhere to Declaration of Helsinki and Good Clinical Practice (GCP) principles * Familiarity with oncology medications and pharmaceutical approach * Ability to work within many software programs

University of Michigan Health is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected Veteran status.

#LI-MA1

Job Family
Registered Nurses/Nursing Leadership
Requirements:
Shift
Days
Degree Type / Education Level
Bachelor's
Status
Full-time
Facility
Sparrow Hospital
Experience Level
4-9 Years
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About Sparrow Health System

Sourced by ZipRecruiter

Sparrow Health System, located in Lansing, MI, US, is a prominent player in the healthcare industry housing a network of hospitals and healthcare facilities. With an official website at sparrow.org, the system was established in 1896, thereby possessing over a century's worth of experience in providing top-tier medical care. It is driven by a vision to be nationally recognized as a leader in quality and Patient experience. The organization's mission is to improve the health of the people in the communities they serve.

Industry

Health care and social assistance

Company size

1,001 - 5,000 Employees

Headquarters location

Lansing, MI, US

Year founded

1896

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