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Study Management Associate Jobs in Flint, MI (NOW HIRING)

McLaren

Dosimetrist I

Flint, MI · On-site

Performs image registration and fusion for diagnostic image studies and previous CT simulations for ... Required: * Bachelor's degree in medical dosimetry or related field (Associate's Degree or ...

Amrize

Sales Intern

Saginaw, MI

$14 - $19/hr

Frequent contact and support via phone with Duro-Last customers and associates, assisting with ... Seeking college degree Field of Study Preferred * Management/Sales/Marketing/Communications or ...

McLaren Flint

Dosimetrist I

Flint, MI

Performs image registration and fusion for diagnostic image studies and previous CT simulations for ... Required: * Bachelor's degree in medical dosimetry or related field (Associate's Degree or ...

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All JobsStudy Management Associate JobsStudy Management Associate Jobs in Flint, MI

Study Management Associate information

See Flint, MI salary details

$9

$36

$52

How much do study management associate jobs pay per hour?

As of Jul 28, 2026, the average hourly pay for study management associate in Flint, MI is $36.56, according to ZipRecruiter salary data. Most workers in this role earn between $24.17 and $47.68 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Study Management Associate, and why are they important?

To thrive as a Study Management Associate, you need strong organizational skills, attention to detail, and a background in life sciences or clinical research, often supported by a relevant bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines such as GCP are typically required. Effective communication, time management, and problem-solving abilities help facilitate collaboration among cross-functional teams and ensure smooth study execution. These skills are crucial for maintaining the quality, compliance, and efficiency of clinical studies.

What is the difference between Study Management Associate vs Clinical Research Coordinator?

AspectStudy Management AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, often with certifications like CCRP
Work EnvironmentPharmaceutical companies, CROs, research institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed in industry-sponsored trials and clinical research firmsCommon in academic and hospital-based studies
Search & Comparison IntentHigh overlap in job duties and qualificationsSimilar roles with some operational differences

The Study Management Associate and Clinical Research Coordinator roles share many similarities, including required education and work environments. However, the Study Management Associate typically focuses on supporting study operations within industry settings, while the Clinical Research Coordinator often manages patient interactions and site activities in clinical settings. Both roles are essential in advancing clinical research but differ slightly in scope and daily responsibilities.

What are the typical responsibilities of a Study Management Associate in a clinical research team?

As a Study Management Associate, you will play a key role in supporting clinical trials by coordinating study logistics, maintaining essential documentation, and ensuring compliance with regulatory guidelines. Your daily tasks may include organizing meetings, tracking study progress, preparing reports, and liaising with clinical sites and vendors. You will work closely with study managers, clinical research associates, and data management teams to ensure trials run smoothly and efficiently. This collaborative environment provides valuable exposure to various aspects of clinical research and can serve as a strong foundation for career advancement within the industry.

What is a Study Management Associate?

A Study Management Associate is a professional who supports the planning, coordination, and execution of clinical trials or research studies. They typically assist study managers or project leads by handling administrative tasks, maintaining study documentation, and ensuring compliance with regulatory guidelines. Their responsibilities may include scheduling meetings, tracking study progress, managing study supplies, and liaising with study sites or vendors. This role is essential for keeping research studies organized and running efficiently.
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What cities near Flint, MI are hiring for Study Management Associate jobs? Cities near Flint, MI with the most Study Management Associate job openings:
Study Management Associate jobs near you
Associate Director Research Operations

Associate Director Research Operations

Insight

Flint, MI

Full-time

Posted 4 days ago

Job description

Insight Health System Clinical Research

JOB DESCRIPTION

Associate Director, Research Operations

Title: Associate Director – Research Operations
Location: Michigan
Reports To: Director of Research Operations
Schedule: Full-time, with flexibility for study visits, sponsor meetings, and operational needs

Position Summary:
The Associate Director of Research Operations is responsible for supporting Insight Health System’s clinical research enterprise across multiple sites. This role is 50% focused on clinical Trials operations oversight and 50% dedicated to central feasibility, start up, regulatory, contracts and budgets, and quality functions. The Associate Director ensures operational excellence, compliance, and efficient execution of research activities across the network.

Key Responsibilities:


Clinical Operations Leadership (50%):
• Oversee day-to-day clinical research operations across assigned regions/sites
• Support site managers, team leads, coordinators, assistants, and investigators to ensure protocol adherence and visit execution
• Monitor enrollment performance, visit scheduling, and resource allocation
• Troubleshoot operational barriers and implement workflow improvements
• Support onboarding, training, and competency development for research staff

• Capability of travel between multiple locations as needed to support operational activities

Feasibility, Regulatory, Contracts, Budgets, and Quality (50%):
• Collaborate with Feasibility and start up/regulatory teams to ensure timely FQ submissions, IRB submissions, amendments, and reporting
• Support contract and budget negotiations, including feasibility review and cost analysis
• Ensure quality standards across documentation, data entry, and essential files
• Participate in internal audits, monitoring visits, and CAPA development
• Maintain alignment with SOPs, GCP, IRB and institutional requirements

  • Review study protocols and develop source

  • Maintain ISF documentation

Cross-Functional Collaboration:
• Serve as a liaison between research operations, regulatory, finance, legal, and executive leadership
• Support strategic planning for site growth, service expansion, and operational scaling
• Contribute to SOP development, process optimization, and system implementation

Minimum Qualifications:
• Ph.d degree in life sciences, healthcare, or related field (required)
• 5–7 years of clinical research experience, including operational leadership
• Strong knowledge of GCP, FDA regulations, IRB processes, and site management
• Experience with budgets, contracts, and regulatory and quality workflows
• Excellent communication, leadership, and problem-solving skills

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