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Clinical Research Associate Bridge Program Jobs in Raleigh, NC

Veranex

Sr Clinical Research Associate

Raleigh, NC · On-site

$98K - $140K/yr

Veranex has an exciting opportunity to join our team as a Senior Clinical Research Associate to support our Clinical Operations team. The Sr. CRA will participate in the planning, development, and ...

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Senior Clinical Research Associate

Cary, NC · Remote

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 ...

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Senior Clinical Research Associate

Cary, NC · Remote

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 ...

IQVIA

Sr. Clinical Research Associate, IQVIA

Durham, NC

$101K - $169K/yr

IQVIA is hiring Senior Clinical Research Associate 1 with experience in either oncology, cardiovascular, renal, metabolic, CNS, Obesity (GLP-1), diabetes, GI, MASH/NASH, dermatology, or respiratory:

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All JobsClinical Research Associate Bridge Program JobsClinical Research Associate Bridge Program Jobs in Raleigh, NC

Clinical Research Associate Bridge Program information

See Raleigh, NC salary details

$11

$39

$67

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

As of Jul 23, 2026, the average hourly pay for clinical research associate bridge program in Raleigh, NC is $39.98, according to ZipRecruiter salary data. Most workers in this role earn between $28.03 and $51.15 per hour, depending on experience, location, and employer.

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

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 types of mentorship and training can I expect as a participant 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 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.
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Clinical Research Associate Bridge Program jobs near you
Infographic showing various Clinical Research Associate Bridge Program job openings in Raleigh, NC as of July 2026, with employment types broken down into 100% Full Time. Highlights an 50% Hybrid, and 50% Remote job distribution, with an average salary of $83,154 per year, or $40 per hour.
Clinical Research Apprentice - DOCR

Clinical Research Apprentice - DOCR

Duke Clinical Research Institute

Durham, NC • On-site

Other

Medical, Dental, Retirement

This job post has expired today. Applications are no longer accepted.

Job description

School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations.

Be You.

The Clinical Research Unit at Duke University is looking for a Clinical Research Apprentice to join our team. This is an exciting opportunity to launch your clinical research career through a full-time apprenticeship supported by Bloomberg Philanthropies. In this role, you will gain hands-on experience while learning directly from experienced Clinical Research Professionals and building foundational skills in clinical trials, participant engagement, data management, and research operations.

You will work alongside research teams supporting studies across a variety of clinical research domains while completing work-based learning experiences designed to increase your knowledge, confidence, and independence over time. This role is ideal for someone passionate about healthcare, research, and improving patient outcomes through clinical discovery.

Minimum Requirements:

  • Associate's degree in Clinical Research or successful completion of the approved Clinical Research Pre-Apprenticeship program
  • Completion of the Durham Technical Community College Clinical Trials Research Associate's Degree training is required as a pre-requisite of the apprenticeship
  • Ability to use standard computing software and web-based applications, including Microsoft Office products
  • Strong communication and organizational skills
  • Ability to work collaboratively in a team-based environment
  • Interest in clinical research and participant-centered care

Preferred Qualifications:

  • Prior exposure to healthcare or clinical environments
  • Familiarity with electronic health records (EHR) or research databases
  • Demonstrated attention to detail and ability to follow standard operating procedures
  • Interest in learning Good Clinical Practice (GCP) and regulatory requirements

Other Requirements:

  • Ability to attend departmental training sessions and professional development opportunities
  • Ability to perform study-related administrative and operational tasks
  • Some roles may involve specimen handling and management of research supplies

This position is:

  • Onsite. The work is performed on-site or at a designated assignment location.

Be Bold.

In this role, you will:

  • Perform clinical research tasks under supervision while increasing independence over time
  • Assist with study participant screening, recruitment, scheduling, and study visit preparation
  • Collect, document, and maintain participant and study-level information in compliance with protocols and SOPs
  • Support specimen handling, inventory management, and investigational product accountability
  • Enter and review research data for accuracy, completeness, and quality assurance
  • Assist with informed consent documentation and participant communication
  • Participate in study team meetings, monitoring visits, and audit preparation activities
  • Learn and apply Good Clinical Practice (GCP), research ethics, and participant safety standards
  • Collaborate with mentors and research professionals to develop clinical research competencies

and apply Good Clinical Practice (GCP), research ethics, and participant safety standards

Choose Duke.

At Duke University, you will join a collaborative research environment dedicated to advancing healthcare and scientific discovery. Through mentorship, hands-on learning, and structured professional development, you will gain valuable skills that prepare you for long-term success in clinical research.

Duke is committed to creating a community built on collaboration, innovation, creativity, and belonging. We value diverse perspectives and foster an environment where every team member feels respected, supported, and empowered to contribute.

Duke University is an Equal Opportunity Employer committed to providing employment opportunity without regard to age, color, disability, gender, gender identity or expression, genetic information, national origin, race, religion, sexual orientation, pregnancy-related conditions, or military status.


Anticipated Pay Range: Duke University provides an annual base salary range for this position as USD $20.76 to USD $31.44. Duke University considers factors such as (but not limited to) scope and responsibilities of the position; candidate's work experience, education/training, and key skills; internal peer equity; as well as market and organizational considerations when extending an offer.


Your total compensation goes beyond the dollars on your paycheck. Duke provides comprehensive and competitive medical and dental care programs, generous retirement benefits, and a wide array of family-friendly and cultural programs to eligible team members. Learn more at: https://hr.duke.edu/benefits/


Equal Opportunity Employer: Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex (including pregnancy and pregnancy- related conditions), sexual orientation, or military status.


Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas-an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values.


Essential Physical Job Functions:
Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and reasonable accommodation(s) can be requested with Duke Access and Accommodations Services (email: DAAS@duke.edu; phone: 919-668-1267).

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