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Clinical Project Manager Jobs in Michigan (NOW HIRING)

Project Manager - Clinical Research Training and Quality The Project Manager will serve as a key member of the Quality team, supporting the Cancer, Clinical Trials, and Translational Research Office ...

Project Manager - Clinical Research Training and Quality The Project Manager will serve as a key member of the Quality team, supporting the Cancer, Clinical Trials, and Translational Research Office ...

It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic ... The Project Manager is accountable for coordinating and managing clients' projects through all ...

It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic ... The Project Manager is accountable for coordinating and managing clients' projects through all ...

Position Title * Senior IT/Technical Project manager Position Responsibilities Senior IT/Technical Project manager Hybrid onsite from day 1 (3 days onsite 2 days remote) Lansing Michigan (look for ...

Project Manager

Fraser, MI · On-site

$125K/yr

Project Manager Minimum 2 Years experience as a Project Manager Venteon is currently seeking an experienced Project Manager to fill a opening with a construction company located in Metro Detroit. The ...

Project Manager

Walker, MI · On-site

$65.18/hr

Project Manager Duration: 2 year (24 months) Contract Location: Walker MI USA 49534 Shift: Business hours Pay Ra nge: $55/hr. - $65/hr. On W2. Description: The experienced Project Manager be ...

This position is for a Senior Project Manager (PM3) to assist the State of Michigan Project Management Office supporting Michigan Department of Treasury with a multi-year high priority project. This ...

Experienced Senior Project Manager for managing multiple complex IT Infrastructure projects/programs with strong communication skills. Experience with IT Audits, Audit Monitoring, Governance and ...

The primary focus for this Project Manager will be to manage the project(s) to merge the identity systems for sales & manufacturing into a single solution. The Project Manager will be responsible for ...

Project Manager

Grand Rapids, MI · On-site

$100K - $125K/yr

Project Manager Axis Automation is looking for a career-oriented Project Manager to join a dynamic, tight-knit team creating custom factory automation equipment. Our team has decades of automation ...

Summary We are seeking a highly organized, certified Project Manager to lead cross-functional initiatives within our aftermarket automotive business. This individual will oversee the full lifecycle ...

Project Manager

Walker, MI · On-site

$100K - $125K/yr

Project Manager Axis Automation is looking for a career-oriented Project Manager to join a dynamic, tight-knit team creating custom factory automation equipment. Our team has decades of automation ...

... Clinic Operations Project Manager. This key leadership role will oversee enterprise-wide ... Collaborate with clinical, administrative, and IT teams to align resources, remove obstacles, and ...

Project Manager

Walker, MI · On-site

$100K - $125K/yr

Project Manager Axis Automation is looking for a career-oriented Project Manager to join a dynamic, tight-knit team creating custom factory automation equipment. Our team has decades of automation ...

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Showing results 1-20

Clinical Project Manager information

See Michigan salary details

$25

$52

$94

How much do clinical project manager jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for clinical project manager in Michigan is $52.91, according to ZipRecruiter salary data. Most workers in this role earn between $36.88 and $62.02 per hour, depending on experience, location, and employer.

What is the difference between Clinical Project Manager vs Clinical Research Associate?

AspectClinical Project ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, with many holding advanced degrees or certifications like PMPUsually holds a Bachelor's degree in life sciences or related field; certifications like CRA certification are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates with sponsors and sitesMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageFound in pharmaceutical, biotech, and CRO companies overseeing entire projectsPrimarily employed by CROs and sponsors to monitor trial sites

The Clinical Project Manager and Clinical Research Associate roles are closely related but differ mainly in scope. The Clinical Project Manager oversees entire clinical trials, manages teams, and coordinates with stakeholders, while the Clinical Research Associate focuses on monitoring clinical sites and ensuring protocol adherence. Both roles require similar educational backgrounds and certifications, but their responsibilities and work environments differ significantly.

What Does a Clinical Project Manager Do?

A clinical project manager, or CPM, manages clinical trial studies for new drugs and medical devices. In this clinical management position, responsibilities and duties include working with all team members and all aspects of a clinical project, including subject selection and enrollment, record keeping, process auditing, and documentation. They also work with the budget and communicate with third parties, such as laboratories or investigators.

What are the key skills and qualifications needed to thrive as a Clinical Project Manager, and why are they important?

To thrive as a Clinical Project Manager, you need expertise in clinical trial management, regulatory compliance, and a relevant life sciences degree, often supported by experience in clinical research. Familiarity with project management tools, electronic data capture (EDC) systems, and certifications like PMP or ACRP are highly valued. Strong leadership, problem-solving, and communication skills help you effectively coordinate teams and stakeholders. These competencies ensure successful trial execution, regulatory adherence, and timely project delivery in a highly regulated environment.

What does a Clinical Project Manager do?

A Clinical Project Manager oversees the planning, execution, and completion of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They coordinate teams, manage budgets, timelines, and ensure that studies comply with regulatory standards and company protocols. Clinical Project Managers act as the main point of contact between sponsors, vendors, and clinical research sites, working to ensure that trials progress smoothly and data integrity is maintained. Their role is critical in bringing new therapies and treatments to market safely and efficiently.

What are some common challenges Clinical Project Managers face when coordinating multi-site clinical trials?

Clinical Project Managers often encounter challenges such as maintaining consistent communication across different sites, ensuring adherence to regulatory guidelines, and managing timelines amidst unexpected delays. Coordinating multi-site trials requires balancing the needs of diverse teams, addressing site-specific issues, and ensuring data quality across all locations. Effective project management tools, regular status meetings, and proactive risk assessment are essential for overcoming these obstacles and keeping the study on track.
What are the most commonly searched types of Clinical Project jobs in Michigan? The most popular types of Clinical Project jobs in Michigan are:
What are popular job titles related to Clinical Project Manager jobs in Michigan? For Clinical Project Manager jobs in Michigan, the most frequently searched job titles are:
What job categories do people searching Clinical Project Manager jobs in Michigan look for? The top searched job categories for Clinical Project Manager jobs in Michigan are:
What cities in Michigan are hiring for Clinical Project Manager jobs? Cities in Michigan with the most Clinical Project Manager job openings:
Infographic showing various Clinical Project Manager job openings in Michigan as of July 2026, with employment types broken down into 95% Full Time, and 5% Contract. Highlights an 100% In-person job distribution, with an average salary of $110,049 per year, or $52.9 per hour.
Project Manager

Project Manager

Actalent

Detroit, MI

Contractor

Medical, Dental, Vision, Life, Retirement, PTO

Posted 7 days ago


Job description

Job Title: Project Manager – Clinical Research Training and Quality
Job Description

The Project Manager will serve as a key member of the Quality team, supporting the Cancer, Clinical Trials, and Translational Research Office by leading education and training initiatives. This role focuses on ensuring that all team members complete required training and remain compliant with regulatory and institutional standards, while also designing and implementing new training content. The position requires a strong understanding of clinical research operations, patient care, data management, and regulatory processes, with a particular emphasis on treatment-based clinical trials rather than observational studies.

Responsibilities

  • Lead education and training initiatives for the Quality team supporting cancer, clinical trials, and translational research activities.
  • Ensure all staff complete required training and maintain ongoing compliance with regulatory, institutional, and departmental requirements.
  • Develop, update, and deliver new training content tailored to Research Assistants, Regulatory staff, Clinic Coordinators, Data Coordinators, Nurses, and administrative personnel.
  • Monitor and track training completion, documentation, and adherence to training schedules across the department.
  • Understand and oversee protocol review and execution processes to ensure consistency, quality, and regulatory compliance.
  • Maintain and manage schedules of adherence for clinical trial protocols, ensuring timelines and milestones are met.
  • Assess and support site workflows to promote efficient, compliant, and patient-centered clinical research operations.
  • Apply comprehensive knowledge of regulatory processes to guide training content and quality initiatives.
  • Interpret applicable regulations and translate them into clear, practical training materials and guidance for staff.
  • Educate and train staff on regulatory requirements, treatment protocols, and best practices in clinical research.
  • Collaborate with clinical and administrative teams involved in contracts, regulatory submissions, and trial operations to align training with operational needs.
  • Support audit readiness by preparing staff and documentation for sponsor, internal, and FDA audits.
  • Participate in or support sponsor, internal, and FDA audits, ensuring training and quality processes meet required standards.
  • Focus on treatment protocols, ensuring training and processes address the complexities of interventional clinical trials rather than observational studies.
  • Contribute to continuous improvement initiatives that enhance the quality of training, patient care, data integrity, and regulatory compliance.
  • Indirectly support patient care outcomes by improving staff competency and adherence to clinical research standards.
  • Collaborate closely with another coordinator and leadership to prioritize training projects and quality initiatives within the department.
  • Provide subject matter expertise on clinical research, patient care, data management, and regulatory requirements to inform departmental policies and procedures.
Essential Skills
  • At least five years of research experience, with exposure to all aspects of clinical research operations.
  • Demonstrated experience in clinical research and clinical trials, particularly treatment-based protocols rather than observational trials.
  • Strong understanding of patient care within the context of clinical research.
  • Clinical research certification or equivalent formal recognition in clinical research practices.
  • Proven knowledge of regulatory compliance requirements for clinical research.
  • Ability to understand, interpret, and apply regulations to real-world clinical research scenarios.
  • Experience educating or training others on regulations, protocols, and compliance requirements.
  • Participation in sponsor, internal, or FDA audits, with familiarity in audit expectations and processes.
  • Comprehensive understanding of protocol review, execution, and documentation requirements.
  • Experience maintaining schedules of adherence for clinical trial activities and site workflows.
  • Broad experience with research, patient care, data management, and regulatory processes in a clinical research setting.
Additional Skills & Qualifications
  • Experience in oncology clinical research, including familiarity with oncology-specific protocols and workflows.
  • Background in training development, including designing, organizing, and delivering training programs.
  • Experience with audit preparation, including organizing documentation and coaching staff for sponsor, internal, or FDA audits.
  • Ability to collaborate effectively with diverse roles such as Research Assistants, Regulatory staff, Clinic Coordinators, Data Coordinators, Nurses, and administrative teams.
  • Strong communication and presentation skills to clearly convey complex regulatory and clinical concepts.
  • Interest in professional growth, with openness to future opportunities within the department or broader organization.
Work Environment

The Project Manager will work within the Cancer, Clinical Trials, and Translational Research Office alongside a small, collaborative team that includes another coordinator and a manager. The position follows a hybrid work model, requiring on-site presence two days per week and remote work for the remaining three days. On-site days vary week to week based on meetings, audits, and departmental activities. Initially, the schedule will align with the manager’s on-site days to support onboarding and collaboration, and over time will offer some flexibility in selecting remote and on-site days, subject to meeting and audit schedules. The environment centers on complex oncology clinical trials and translational research, with a strong emphasis on quality, regulatory compliance, and continuous improvement. The culture supports professional development and offers opportunities to move into other roles within the department or broader organization, while providing a setting where training initiatives can have a meaningful impact on both staff performance and patient care.

Job Type & Location

This is a Contract to Hire position based out of Detroit, MI.

Pay and Benefits

The pay range for this position is $32.00 - $67.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a hybrid position in Detroit,MI.

Application Deadline

This position is anticipated to close on Jul 17, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.


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About Actalent

Sourced by ZipRecruiter

Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We're supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.

Company size

5,001 - 10,000 Employees

Headquarters location

Hanover, MD, US

Year founded

1983

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