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Clinical Research Associate Bridge Program Jobs in Center Line, MI

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 ...

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 ...

Georgetown University

Clinical Research Nurse

Detroit, MI · On-site

$54.62 - $100.49/hr

S. Supreme Court, Georgetown University offers rigorous academic programs, a global perspective ... Job Overview The Clinical Research nurse, Lombardi Cancer Center - Georgetown University, is a ...

New

Actalent

Clinical Research Coordinator-Thoracic

Detroit, MI · On-site

$24 - $31.75/hr

Clinical Research Coordinator This role focuses on coordinating complex clinical drug trials ... Employee Assistance Program; Time Off/Leave (PTO, Vacation or Sick Leave). Workplace Type: This is ...

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All JobsClinical Research Associate Bridge Program JobsClinical Research Associate Bridge Program Jobs in Center Line, MI

Clinical Research Associate Bridge Program information

See Center Line, MI salary details

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How much do clinical research associate bridge program jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for clinical research associate bridge program in Center Line, MI is $38.63, according to ZipRecruiter salary data. Most workers in this role earn between $27.12 and $49.42 per hour, depending on experience, location, and employer.

What is a Clinical Research Associate Bridge Program?

A Clinical Research Associate (CRA) Bridge Program is a specialized training course designed to help individuals transition into the role of a CRA, especially those with related experience in healthcare, life sciences, or clinical research support. These programs typically combine classroom instruction with practical training, focusing on topics such as clinical trial monitoring, regulatory compliance, and Good Clinical Practice (GCP) guidelines. The goal is to equip participants with the necessary knowledge and skills to begin a career as a CRA, often including job placement assistance or internships. Bridge programs are ideal for those who want to move into clinical research from a related field but lack direct CRA experience.

What types of mentorship and training can I expect in a Clinical Research Associate Bridge Program?

Participants in a Clinical Research Associate (CRA) Bridge Program typically receive structured mentorship from experienced CRAs and clinical research professionals. The program often includes hands-on training in protocol review, site monitoring, regulatory compliance, and data management, combined with classroom or online learning modules. You'll work closely with cross-functional teams, such as clinical project managers and regulatory specialists, gaining exposure to industry-standard processes and tools. This supportive environment is designed to accelerate your transition into a CRA role and help you build a strong professional network within clinical research.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate in a bridge program?

To thrive as a Clinical Research Associate in a bridge program, you need a foundational understanding of clinical trials, regulatory compliance, and data management, usually supported by a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, effective communication, and organizational skills help you manage study protocols and collaborate with diverse teams. These competencies are crucial for ensuring clinical trial integrity, regulatory adherence, and the successful execution of research studies.

What job categories do people searching Clinical Research Associate Bridge Program jobs in Center Line, MI look for?

The top searched job categories for Clinical Research Associate Bridge Program jobs in Center Line, MI are:

What cities near Center Line, MI are hiring for Clinical Research Associate Bridge Program jobs?

Cities near Center Line, MI with the most Clinical Research Associate Bridge Program job openings:

Clinical Research Associate Bridge Program jobs near you

Clinical Research Associate II/Sr. CRA

ICON

Detroit, MI

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 21 days ago

Job description

CRA II/Sr. CRA- Detroit, MI
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 CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports

Your Profile:
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:
  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • 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 request here.
Are you a current ICON Employee? Please click here to apply

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