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Clinical Research Associate Intern Jobs in Michigan

ICON

Clinical Research Associate

Detroit, MI · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Research Associate - Oncology - Detroit, MI ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Icon plc

Clinical Research Associate

Detroit, MI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Research Associate - Oncology - Detroit, MI ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Becton, Dickinson and Company

  • Medical

  • Life

The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical operations professional responsible for managing site monitoring and relationship activities across multiple clinical ...

Icon plc

Clinical Research Associate II/Sr. CRA

Detroit, MI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. * Strong organizational and communication ...

ICON

Clinical Research Associate II/Sr. CRA

Detroit, MI · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. * Strong organizational and communication ...

BAMF Health

Clinical Research Nurse- Start Up

Grand Rapids, MI · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Associate's degree in nursing required * 2 years of RN experience in a healthcare setting required ... intern, or volunteer based upon the following characteristics: race, color, religion, creed ...

BAMF Health

Clinical Research Nurse- Start Up

Grand Rapids, MI · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Associate's degree in nursing required * 2 years of RN experience in a healthcare setting required ... intern, or volunteer based uponthe following characteristics: race, color, religion, creed ...

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All JobsClinical Research Associate Intern JobsClinical Research Associate Intern Jobs in Michigan

Clinical Research Associate Intern information

See Michigan salary details

$1.8K

$5.6K

$6.8K

How much do clinical research associate intern jobs pay per month?

As of Aug 15, 2026, the average monthly pay for clinical research associate intern in Michigan is $5,612.67, according to ZipRecruiter salary data. Most workers in this role earn between $3,850.00 and $6,683.33 per month, depending on experience, location, and employer.

What does a clinical research associate intern do?

A Clinical Research Associate Intern assists in the monitoring and coordination of clinical trials to ensure they are conducted according to regulatory standards and study protocols. Interns may help with site visits, data collection, documentation, and communication between research teams and sponsors. This role provides hands-on experience in clinical research processes and helps interns develop an understanding of Good Clinical Practice (GCP) guidelines. Interns often work under the supervision of experienced clinical research professionals and gain valuable insight into the pharmaceutical or medical device industry.

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

AspectClinical Research Associate InternClinical Research Coordinator
Required CredentialsTypically pursuing or holding a degree in life sciences; some internships require minimal certificationsUsually holds a bachelor's degree in health sciences or related field; certifications like CCRP are common
Work EnvironmentInternship setting within pharmaceutical companies or research institutions; supervised learningActive role in clinical trial sites; responsible for daily trial operations
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutions for trainingEmployed directly at clinical sites, hospitals, or research centers

While both roles involve clinical trial processes, a Clinical Research Associate Intern is primarily a learning position focusing on gaining experience, whereas a Clinical Research Coordinator manages the day-to-day operations of clinical trials at research sites.

What typical challenges do clinical research associate interns encounter when monitoring clinical trial sites?

Clinical Research Associate Interns often face challenges such as ensuring accurate data collection, maintaining regulatory compliance, and communicating effectively with site staff. Balancing these responsibilities while learning industry protocols can be demanding, especially when managing multiple sites or studies. Interns are supported by experienced team members, but must quickly adapt to varying site workflows and documentation standards to ensure trial integrity.

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

To thrive as a Clinical Research Associate Intern, you need a solid understanding of clinical trial protocols, regulatory guidelines (like GCP), and typically a background in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certifications like GCP training are highly valued. Strong attention to detail, organizational skills, and effective communication help interns excel in monitoring studies and collaborating with site staff. These skills are crucial for ensuring data integrity, regulatory compliance, and the smooth operation of clinical research projects.

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

The most popular types of Clinical Research Intern jobs in Michigan are:

What are popular job titles related to Clinical Research Associate Intern jobs in Michigan?

For Clinical Research Associate Intern jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Clinical Research Associate Intern jobs in Michigan look for?

The top searched job categories for Clinical Research Associate Intern jobs in Michigan are:

What cities in Michigan are hiring for Clinical Research Associate Intern jobs?

Cities in Michigan with the most Clinical Research Associate Intern job openings:

Clinical Research Associate Intern jobs near you
Infographic showing various Clinical Research Associate Intern job openings in Michigan as of August 2026, with employment types broken down into 2% As Needed, 73% Full Time, 16% Part Time, 1% Temporary, and 8% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $67,352 per year, or $32.4 per hour.

Clinical Research Associate

410 ICR United States USA

Detroit, MI

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 4 hours ago

Job description

Clinical Research Associate - Oncology - Detroit, MI

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


What You Will Be Doing:

  • Serve as the primary point of contact between investigational sites and the sponsor - Oncology

  • Conduct all types of site visits, including selection, initiation, routine monitoring, and close-out

  • Ensure site compliance with ICH-GCP, SOPs, and regulations

  • Maintain up-to-date documentation in CTMS and eTMF systems

  • Support and track site staff training and maintain compliance records

  • Monitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting

  • Support subject recruitment and retention efforts at the site level

  • Oversee drug accountability and ensure proper storage, return, or destruction

  • Resolve data queries and drive timely, high-quality data entry

  • Document site progress and escalate risks or issues to the clinical team

  • Assist in tracking site budgets and ensuring timely site payments (as applicable)

  • Collaborate with cross-functional partners including CTAs, LTMs, and CTMs

You are:

  • A graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RN

  • Eligible to work in United States without visa sponsorship

  • A clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry

  • Experienced monitoring oncology clinical trials.

  • Proficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF

  • A clear communicator, problem-solver, and collaborative team player

  • Willing and able to travel up to 50% for on-site monitoring visits across Midwest region; preference given to candidates residing in Detroit near major HUB airports to support efficient regional travel


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply