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Part Time Clinical Research Associate Jobs in Detroit, MI

IQVIA

MedTech Part Time Clinical Consultant

Detroit, MI · On-site

$60/hr

... clinical research services, commercial insights and healthcare intelligence to the life sciences ... part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of ...

Smile Partners USA

Oral Surgeon

Shelby, MI · On-site

$267K - $353K/yr

Associate Oral Surgeon Opportunity Shelby Township, MI Shelby Oral Surgery Dr. Joseph M. Hildebrand ... Khazaal Part-Time Clinical Scope The ideal candidate will be comfortable providing a full range of ...

Smile Jobs

Oral Surgeon

Utica, MI · On-site

$276K - $364K/yr

Associate Oral Surgeon Opportunity - Shelby Township, MI Shelby Oral Surgery - Dr. Joseph M ... Khazaal - Part-Time Clinical Scope The ideal candidate will be comfortable providing a full range ...

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All JobsClinical Research Associate JobsPart Time Clinical Research Associate JobsPart Time Clinical Research Associate Jobs in Detroit, MI

Part Time Clinical Research Associate information

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$11

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$69

How much do part time clinical research associate jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for part time clinical research associate in Detroit, MI is $40.71, according to ZipRecruiter salary data. Most workers in this role earn between $28.56 and $52.12 per hour, depending on experience, location, and employer.

What is a part time clinical research associate?

Part-time Clinical Research Associates (CRAs) are professionals who monitor and manage clinical trials on a flexible or reduced-hour schedule, rather than full-time. They are responsible for ensuring that studies comply with regulatory requirements, collecting data, and acting as a liaison between clinical trial sites and sponsors. Part-time CRAs may work remotely or travel to research sites as needed, and their schedules can vary depending on the needs of the research project. This role is ideal for those seeking work-life balance or supplementing other professional activities. Their work is critical in advancing medical research and ensuring patient safety.

What are the key skills and qualifications needed to thrive as a part time clinical research associate?

To thrive as a Part Time Clinical Research Associate, you need a background in life sciences or healthcare, knowledge of clinical research protocols, and often a bachelor’s degree in a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and sometimes certification such as ACRP or SOCRA is highly valued. Strong attention to detail, organizational skills, and effective communication are essential soft skills for monitoring trials and collaborating with research teams. These skills ensure regulatory compliance, accurate data collection, and efficient trial execution, all critical for successful clinical research outcomes.

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

Part-time Clinical Research Associates (CRAs) often face the challenge of balancing multiple study sites and projects within limited working hours. Time management and clear communication with both the research team and site staff are crucial to ensure all monitoring visits, documentation, and regulatory requirements are met on schedule. Additionally, part-time CRAs may need to be proactive in staying updated on study protocols and industry regulations, as they may not be present for all in-person team meetings. Establishing structured routines and leveraging digital tools for remote collaboration can help manage these challenges effectively.

What is the difference between Part Time Clinical Research Associate vs Clinical Research Coordinator?

AspectPart Time Clinical Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often certifications like CCRP or RACBachelor's degree, often certifications like CCRP or RAC
Work EnvironmentMonitoring clinical trials at sites, remote or onsiteManaging trial operations at research sites
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinics
Search & Comparison IntentUnderstanding monitoring roles in trialsManaging trial activities at sites

Part Time Clinical Research Associates primarily focus on monitoring clinical trial progress, ensuring compliance, and verifying data accuracy, often working remotely or onsite. Clinical Research Coordinators handle the day-to-day operations at research sites, including patient recruitment and data collection. Both roles require similar credentials but differ in responsibilities and work settings.

What are the most commonly searched types of Part Time Clinical Research jobs in Detroit, MI?

The most popular types of Part Time Clinical Research jobs in Detroit, MI are:

What are popular job titles related to Part Time Clinical Research Associate jobs in Detroit, MI?

For Part Time Clinical Research Associate jobs in Detroit, MI, the most frequently searched job titles are:

What job categories do people searching Part Time Clinical Research Associate jobs in Detroit, MI look for?

The top searched job categories for Part Time Clinical Research Associate jobs in Detroit, MI are:

Part Time Clinical Research Associate jobs near you
Infographic showing various Part Time Clinical Research Associate job openings in Detroit, MI as of August 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution, with an average salary of $84,683 per year, or $40.7 per hour.

Clinical Research Coordinator (Part-Time)

Garden City, MI • On-site

Professional Case Management
Health Care and Social Assistance • 201 - 500 employees

5.0

Company rating: 5.0 out of 10

Based on 10 frontline employees who took The Breakroom Quiz

Great coworkers

People enjoy working here

Recommended by parents

Learn more about Professional Case Managementexternal

$23 - $30.50/hr

Part-time

Medical, Dental, Vision, Retirement, PTO

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

Job description

Put your talents to work at PCM! Whether you work in our Home Care, Clinical Research, Impairments, or Catastrophic Care division, you will support our mission to deliver care and other services that enhance the quality of life of our clients. Be a part of our dynamic client-focused team and make a difference in your career!
As an on-site Clinical Research Coordinator (CRC), you will provide technical and administrative support to your assigned clinical operations team in the field as well as direct patient care of research study participants. You work with a high attention to detail, reviewing documentation, coordinating clinical study project details, and maintaining data systems - all with a sense of urgency aligned with that of our customers. The position will involve the conduct of trial coordinator activities for EmVenio Research' decentralized network. This will include assessing and following trial participants along with other trial protocol-related activities. In this role the CRC is accountable for the regulatory compliance and performance of assigned mobile clinics and clinician teams conducting decentralized trials as well as patient engagement, and screening. Additional focus will be on timely and accurate EDC data entry and query resolution.
QUALIFICATIONS
  • Bachelor's degree (B. A. / B. S.) from four-year college or university or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills, and abilities

  • Two (2) years research experience strongly preferred. Phlebotomy and ECGs experience not required, but preferred.

  • ACRP or SOCRA Clinical Research Certification (Preferred), Clinical Research Training Certification (Preferred)

  • Excellent computer skills, proficient in MS Word, Excel, PowerPoint and ability to obtain knowledge and master all clinical trial database systems.

  • Proven ability to successfully coordinate multiple studies adhering to regulatory and institutional guidelines.

  • Proven ability to communicate effectively within an interdisciplinary team to ensure safe, efficient, quality patient care, both in-person and virtually.

  • Excellent organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively.

  • Ability to effectively analyze project specific data/systems to ensure accuracy and efficiency.

  • Flexibility to reprioritize workload to meet changing project timelines.

  • Responsible for adhering to FDA Good Clinical Practices, FDA regulations, EmVenio Research/Client Standard Operating Procedures and Working Practice Documents regulations for all non-clinical/clinical aspects of project implementation, execution, and closeout.

  • Ability to successfully complete EmVenio Research clinical training program.

  • Able to perform successfully under pressure while prioritizing and handling multiple projects or activities.

  • Must have strong interpersonal skills to be able to interact with multiple people on many different levels.

  • May be responsible for basic clinical assessments.

ESSENTIAL FUNCTIONS/AREAS OF ACCOUNTABILITY
  • Complete study tasks as outlined by trial protocol

  • Ensures documentation is accurate according to EmVenio guidelines and protocols is required

  • Achieves EmVenio standards for quality, customer service, productivity and teamwork through participation in Risk and Quality Improvement programs, clinical meetings and other meetings as required

  • Works collaboratively with nurses, physicians, nurse practitioners, physician assistants, clinical research specialists, leaders, family members, key care givers and any ancillary medical personnel as appropriate

  • Communicates with key stakeholders such as the Principal Investigator, clinical trials team and quality department, regulatory

  • Certain assignments may require provider to perform ECGs, draw blood (Phlebotomy), process and ship lab specimen, etc.

  • Consults with the Site Manager and virtual Clinical Research Coordinator to ensure compliance with guidelines

  • Reviews the medical and social history of members

  • Assist in building the community research site network and developing relationships within that community

  • Participates in recruitment of participants to include personally engaging the general public face to face in local across hard-to-reach communities, attending community events, speaking with physicians and people across diverse cultures and backgrounds to support meeting participant enrollment targets

  • Documenting recruiting efforts and outreach progress

  • Facilitates conversations with potential participants through both inbound and outbound calls sometimes serving as their first introduction to research

  • Participates in all mandatory compliance, patient engagement and other training programs, seeks guidance for compliance-related concerns and adheres to all applicable laws, regulations and EmVenio policies and procedures

  • Maintains positive control of all PHI information

  • Participates in required training and education programs

  • Ensures adherence to clinical trial protocols and supports the clinical trials team in ensuring that trials are conducted and comply with all regulatory, state, national and internationally accepted guidelines for Good Clinical Practice (ICH GCP).

  • Ensures timely and accurate data collection and completion of case report forms relevant to clinical trials or research projects.

  • Assists in liaising with monitors of clinical trials and available to monitor and/or audit when required, with full patient documentation available.

  • Assists in educating EmVenio Research staff and participants regarding the designated clinical trial and procedures and relevant investigations associated with the designated clinical trial and to raise the profile of research throughout the EmVenio Research.

  • Any other duties needed to help drive EmVenio's purpose, fulfill our mission, and abide by our core values.

The typical base pay range for this role is USD $28,080 - $38,480 per year.
Individual base pay depends on various factors, in addition to primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience, skills and other market-based factors.
Available Benefits Include
  • Medical
  • Dental
  • Vision
  • 401(k)
  • Company Paid Short Term Disability
  • Flexible Spending Account (FSA)
  • Health Savings Account (HSA)
  • Paid Time Off
  • Voluntary Benefits

Please contact Carson Moreira-Rego at (866) 776-0127 x387 or at Carson.Moreira-Rego@procasemanagement.com today to learn more about our opportunities where you can make a difference in your own career!
Professional Case Management is an Equal Opportunity Employer.
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About Professional Case Management

Sourced by ZipRecruiter

Since 1997, Professional Case Management (PCM) has been providing quality, nationwide in-home nursing services to sufferers of chronic diseases. We are the nation's premier healthcare provider for nuclear weapons workers, uranium miners, millers and haulers suffering from illnesses contracted in the course of their employment. Our mission is to deliver quality care to enhance patient outcomes in the privacy and comfort of their homes.

Industry

Health care and social assistance

Company size

201 - 500 Employees

Headquarters location

Denver, CO, US

Year founded

1986

Social media

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