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Clinical Research Associate Bridge Program Jobs in Farmington, MI

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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Clinical Research Associate Bridge Program information

See Farmington, MI salary details

$11

$40

$68

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

As of Sep 4, 2026, the average hourly pay for clinical research associate bridge program in Farmington, MI is $40.47, according to ZipRecruiter salary data. Most workers in this role earn between $28.37 and $51.78 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 Farmington, MI look for?

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

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

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

Clinical Research Registered Nurse

McLaren Health Care

Detroit, MI • On-site

Other

This job post has expired 3 days ago. Applications are no longer accepted.


McLaren Health Care rating

6.7

Company rating: 6.7 out of 10

Based on 221 frontline employees who took The Breakroom Quiz

534th of 898 rated healthcare providers


Job description

Department: Clinical Research (RN position - Detroit)
Scheduled Bi-Weekly Hours: 80
Shift: Full-Time Days
Daily Work Times: 8:00am-4:30pm
Position Summary:
The CRN is a member of the clinical research team and assists in the recruitment, compliance and follow-up of patients that are eligible for, or registered to a clinical trial. The CRN provides specialized nursing care that ensures exceptional, ethical, safe care yielding high-quality data. Responsible for managing patient standard of care needs as well as participant and protocol needs through application of independent judgment, communication and collaboration with the research patient, patient's family, ancillary/support services, the physician, and the clinical research team.
Responsibilities:

  1. Provides clinical trial support to ensure patients are offered appropriate clinical trials following Good Clinical Practice standards.
  2. Assesses, monitors, evaluates, and documents the patient's compliance and response to protocol treatment
  3. Provides leadership to other members of the clinical team by articulating expected standards of care as directed by the clinical trial. Delegates and supervises other employees, as assigned, to ensure that the clinical trial plan is carried out and that established outcomes are achieved.
  4. Participates in process improvement activities of the department to ensure patient safety.
  5. Demonstrates professionalism and a commitment to improving the work environment through participation in meetings, timely and effective communication, and an embracement of cultural diversity
  6. Provides clinical research support staff with the documentation needed to determine eligibility and maintain compliance

Required
  • Associate Degree from an accredited Nursing program
  • Current State of Michigan Registered Nurse license
  • Two years of nursing experience
Preferred
  • Research experience in designated area of work
  • Nursing experience in area of clinical research focus

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