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Clinical Research Program Manager Jobs in Troy, MI

Actalent

Clinical Research Coordinator

Detroit, MI · Hybrid

$27 - $35/hr

Clinical Research Coordinator (Oncology) About the Role Join a leading cancer research team as a ... Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a ...

Actalent

Clinical Research Coordinator

Detroit, MI · Hybrid

$27 - $35/hr

Clinical Research Coordinator About the Role Join a leading cancer research team as a Clinical ... Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a ...

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All JobsClinical Research Program JobsClinical Research Program Manager JobsClinical Research Program Manager Jobs in Troy, MI

Clinical Research Program Manager information

See Troy, MI salary details

$42.2K

$87.8K

$141.7K

How much do clinical research program manager jobs pay per year?

As of Aug 28, 2026, the average yearly pay for clinical research program manager in Troy, MI is $87,768.00, according to ZipRecruiter salary data. Most workers in this role earn between $68,700.00 and $99,500.00 per year, depending on experience, location, and employer.

What does a clinical research program manager do?

A Clinical Research Program Manager oversees the planning, implementation, and management of clinical research studies within an organization. They coordinate research activities, ensure compliance with regulatory requirements, manage budgets, and supervise research staff. Their role is crucial in maintaining timelines, quality standards, and communication among stakeholders, including investigators, sponsors, and regulatory authorities. They also play a key part in developing study protocols and ensuring that research activities align with organizational goals.

What are the key skills and qualifications needed to thrive as a clinical research program manager?

To thrive as a Clinical Research Program Manager, you need a strong background in clinical research, project management, regulatory compliance, and often an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRP or PMP are typically required. Excellent leadership, organizational, and communication skills set standout managers apart, enabling them to coordinate teams and stakeholders effectively. These skills and qualifications are crucial for ensuring clinical studies meet regulatory standards, stay on schedule, and achieve high-quality outcomes.

What are some typical challenges faced by clinical research program managers in coordinating multi-site studies?

Clinical Research Program Managers often encounter challenges when coordinating multi-site studies, such as ensuring consistent protocol adherence across locations, managing data collection timelines, and addressing site-specific regulatory requirements. Effective communication and strong organizational skills are essential to keep all teams aligned and to resolve issues promptly. Additionally, the role frequently involves collaborating with investigators, sponsors, and regulatory bodies to maintain study integrity and ensure compliance.

What is the difference between Clinical Research Program Manager vs Clinical Research Coordinator?

AspectClinical Research Program ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsTypically holds a bachelor's degree in health sciences or related field
Work EnvironmentOversees multiple studies, manages teams, and coordinates with stakeholdersHandles daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentFocuses on management, oversight, and program coordinationFocuses on study-specific tasks and patient management

The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.

What job categories do people searching Clinical Research Program Manager jobs in Troy, MI look for?

The top searched job categories for Clinical Research Program Manager jobs in Troy, MI are:

What cities near Troy, MI are hiring for Clinical Research Program Manager jobs?

Cities near Troy, MI with the most Clinical Research Program Manager job openings:

Clinical Research Program Manager jobs near you
Infographic showing various Clinical Research Program Manager job openings in Troy, MI as of June 2026, with employment types broken down into 1% As Needed, 65% Full Time, 24% Part Time, and 10% Contract. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $87,768 per year, or $42.2 per hour.

Unblinded Clinical Research Coordinator

DM Clinical Research

Detroit, MI

$24 - $32/hr

Full-time

Re-posted 2 days ago

Job description

Unblinded Clinical Research Coordinator
DM Clinical Research, the largest privately-owned clinical research organization in the Houston area and one of the top fifty in the country, is looking for an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Duties amp; Responsibilities:
  • Compound and dispense prescribed IP.
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans.
  • Provide consultative support regarding the preparation and dosing of drugs.
  • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction.
  • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials.
  • Understand and apply all applicable site procedures.
  • Ensure receipt and proper storage of IP and bioretention samples.
  • Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
  • Review protocols and provide input on clinical and pharmacy supply needs.
  • Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information.
  • Temperature reporting.
  • Any other duties/ tasks assigned by the manager, computer proficiency, especially Word, Excel, Outlook, and Google Docs.

Knowledge amp; Experience:
Education:
  • High School Diploma or equivalent required
  • Foreign Medical Graduate is a plus
  • Pharmacy Technician Certification a plus
Experience:
  • Clinical Experience
Credentials:
  • LPN (Licensed Professional Nurse) or CMA (Certified Medical Assistant)
Knowledge and Skills:
  • Computer proficiency, especially Word, Excel, Outlook, and Google Docs.
  • Excellent communication and customer service skills.
  • Outgoing personality Well-organized with attention to detail.
  • Must be able to multitask.
  • Bilingual (Spanish) preferred but not required

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