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Cra Project Manager Jobs in Romulus, MI (NOW HIRING)

Icon plc

Sr. CRA

Detroit, MI · On-site

$110K - $138K/yr

Senior CRA - Ophthalmology - Midwest ICON is a global healthcare intelligence and clinical research ... Proven ability to manage multiple sites and projects simultaneously, with strong organizational and ...

New

Cisco

Software Architect, Duo

Ann Arbor, MI · On-site +1

$177K - $257K/yr

Understand FedRAMP, CRA, PQC, and related compliance requirements and translate them into ... Project translation will require a good working knowledge of program and project management.

Cra

Senior Analysis Engineer

Farmington Hills, MI · On-site

$102K - $141K/yr

... managers To maintain a working knowledge of new technologies that may improve operations, and develop recommendations accordingly Confer with project staff to outline work-plan and to agree duties ...

CRA, Inc.

Senior Analysis Engineer

Farmington Hills, MI · On-site

$102K - $141K/yr

... managers To maintain a working knowledge of new technologies that may improve operations, and develop recommendations accordingly Confer with project staff to outline work-plan and to agree duties ...

EyeSouth Partners

Ophthalmic Imager ll

Dearborn, MI · On-site

$17.25 - $23.25/hr

... manager * Contribute to the team effort by completing additional tasks or projects as needed ... CRA / ROUB / OCT-C / CDOS certification eligible * Nextech/ICP experience strongly preferred.

EyeSouth Partners LLC

Ophthalmic Imager ll

Livonia, MI · On-site

$16.50 - $22.25/hr

... manager * Contribute to the team effort by completing additional tasks or projects as needed ... CRA / ROUB / OCT-C / CDOS certification eligible * Nextech/ICP experience strongly preferred.

loanDepot

Fair Lending Specialist, Sr

Birmingham, MI · On-site

$70K - $120K/yr

Responsible for executing fair lending risk management initiatives, including performance analytics ... Analyzes Community Reinvestment Act (CRA) performance for applicable state-based requirements ...

loanDepot

Fair Lending Specialist, Sr

Westland, MI · On-site

$70K - $120K/yr

Responsible for executing fair lending risk management initiatives, including performance analytics ... Analyzes Community Reinvestment Act (CRA) performance for applicable state-based requirements ...

loanDepot

Fair Lending Specialist, Sr

Southfield, MI · On-site

$70K - $120K/yr

Responsible for executing fair lending risk management initiatives, including performance analytics ... Analyzes Community Reinvestment Act (CRA) performance for applicable state-based requirements ...

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Showing results 1-20

All JobsCra Project JobsCra Project Manager JobsCra Project Manager Jobs in Romulus, MI

Cra Project Manager information

See Romulus, MI salary details

$46.7K

$89.5K

$153.2K

How much do cra project manager jobs pay per year?

As of Sep 11, 2026, the average yearly pay for cra project manager in Romulus, MI is $89,517.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,100.00 and $111,300.00 per year, depending on experience, location, and employer.

What is a CRA Project Manager?

A CRA Project Manager is a professional who oversees and coordinates clinical research projects, often within pharmaceutical or biotechnology companies or contract research organizations (CROs). They are responsible for planning, executing, and closing clinical trials in compliance with regulatory guidelines. Their duties include managing budgets, timelines, and resources, communicating with stakeholders, and ensuring the quality and integrity of the research data. CRA Project Managers also supervise clinical research associates (CRAs) and ensure that all trial activities adhere to protocols and Good Clinical Practice (GCP) standards.

What are the key skills and qualifications needed to thrive as a CRA Project Manager?

To thrive as a CRA Project Manager, you need a solid background in clinical research, project management expertise, and typically a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), regulatory compliance (such as GCP), and often a project management certification like PMP are highly beneficial. Strong leadership, problem-solving, and communication skills set exceptional candidates apart, especially when managing diverse teams and stakeholders. These skills ensure successful project delivery, regulatory adherence, and effective coordination of clinical research activities.

What are some common challenges faced by a CRA Project Manager when coordinating multi-site clinical trials?

CRA Project Managers often encounter challenges such as ensuring consistent communication across diverse research sites, maintaining regulatory compliance, and managing tight project timelines. They must address site-specific issues quickly while balancing the needs of sponsors, investigators, and regulatory bodies. Success in this role requires strong organizational skills, adaptability, and a proactive approach to problem-solving, as well as the ability to foster collaboration among cross-functional teams.

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

AspectCra Project ManagerClinical Research Associate
CredentialsBachelor's degree, often advanced degrees, project management certificationsBachelor's degree in life sciences or related field, clinical research certifications
Work EnvironmentOversees multiple projects, manages teams, coordinates with sponsorsMonitors clinical trials at sites, ensures protocol compliance
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsPharmaceutical companies, CROs, clinical trial sites

The Cra Project Manager focuses on overseeing entire clinical projects, managing teams, and ensuring timely delivery. In contrast, a Clinical Research Associate primarily monitors clinical trial sites to ensure compliance with protocols. Both roles require related certifications and work within the clinical research industry, but their responsibilities and scope differ significantly.

Cra Project Manager jobs near you

Sr. CRA

Detroit, MI • On-site

Icon plc
See more jobs at Icon plcexternal

$110K - $138K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 3 days ago

New

Job description

Senior CRA - Ophthalmology - Midwest

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.


As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.

What You Will Do:

You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
Key responsibilities include:

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.

  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.

  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.

  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Your Profile:

You will have a strong foundation in clinical trial monitoring, with the experience to work independently and guide others.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field

  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.

  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.

  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.

  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.

  • Experience in Ophthalmology studies required

  • Willingness to travel as required (approximately 60%)


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 requesthere.

Salary Range

$110,520.00-$138,150.00

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

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