Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings ... Position eligible for Employee Referral Program* To apply: Individuals interested in applying for ...
New
Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings ... Position eligible for Employee Referral Program* To apply: Individuals interested in applying for ...
New
Senior Clinical Research Associate
Raleigh, NC · On-site +1
Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings ... Position eligible for Employee Referral Program* To apply: Individuals interested in applying for ...
New
Senior Clinical Research Associate
Raleigh, NC · On-site +1
Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings ... Position eligible for Employee Referral Program* To apply: Individuals interested in applying for ...
New
Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings ... Position eligible for Employee Referral Program* To apply: Individuals interested in applying for ...
New
Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings ... Position eligible for Employee Referral Program* To apply: Individuals interested in applying for ...
New
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 ...
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 ...
Experienced Clinical Research Associate - Hematology/Oncology
Raleigh, NC · Remote
Medical
Retirement
PTO
Through our expedited PACE Training Program, you will receive customized training and efficient ... Clinical Research Associate Experience (minimum 1 year), hematology/oncology exerience preferred
Experienced Clinical Research Associate - Hematology/Oncology
Raleigh, NC · Remote
Medical
Retirement
PTO
Through our expedited PACE Training Program, you will receive customized training and efficient ... Clinical Research Associate Experience (minimum 1 year), hematology/oncology exerience preferred
Senior Clinical Research Associate
Raleigh, NC · Remote
Medical
Dental
Vision
Life
Retirement
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 ...
Senior Clinical Research Associate
Raleigh, NC · Remote
Medical
Dental
Vision
Life
Retirement
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 ...
Senior Clinical Research Associate
Raleigh, NC · Remote
Medical
Dental
Vision
Life
Retirement
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 ...
Senior Clinical Research Associate
Raleigh, NC · Remote
Medical
Dental
Vision
Life
Retirement
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 ...
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 ...
Quick apply
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 ...
Senior Clinical Research Associate
Cary, NC · Remote
Medical
Dental
Vision
Life
Retirement
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 ...
Senior Clinical Research Associate
Cary, NC · Remote
Medical
Dental
Vision
Life
Retirement
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 ...
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 ...
Quick apply
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 ...
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 ...
Quick apply
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 ...
Sr. Clinical Research Associate, IQVIA
Durham, NC · On-site
$87K - $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:
Sr. Clinical Research Associate, IQVIA
Durham, NC · On-site
$87K - $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:
Sr. Clinical Research Associate, IQVIA
Durham, NC · On-site
$87K - $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:
Sr. Clinical Research Associate, IQVIA
Durham, NC · On-site
$87K - $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:
Sr. Clinical Research Associate, IQVIA
$87K - $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:
Sr. Clinical Research Associate, IQVIA
$87K - $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:
Are you a motivated Clinical Research Associate with 2-3 years of monitoring experience who is looking for more than just your next job? Are you seeking a company that will invest in your development ...
Are you a motivated Clinical Research Associate with 2-3 years of monitoring experience who is looking for more than just your next job? Are you seeking a company that will invest in your development ...
Clinical Research Associate 2, IQVIA
Durham, NC · On-site
$71K - $189K/yr
IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...
Clinical Research Associate 2, IQVIA
Durham, NC · On-site
$71K - $189K/yr
IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...
Are you a motivated Clinical Research Associate with 2-3 years of monitoring experience who is looking for more than just your next job? Are you seeking a company that will invest in your development ...
Are you a motivated Clinical Research Associate with 2-3 years of monitoring experience who is looking for more than just your next job? Are you seeking a company that will invest in your development ...
Clinical Research Associate 2, IQVIA
Durham, NC · On-site
$71K - $189K/yr
IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...
Clinical Research Associate 2, IQVIA
Durham, NC · On-site
$71K - $189K/yr
IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...
Clinical Research Associate 2, IQVIA
Durham, NC · On-site
$71K - $189K/yr
IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...
Clinical Research Associate 2, IQVIA
Durham, NC · On-site
$71K - $189K/yr
IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...
You'll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting. We are diverse in many ways, yet our values unite us. Our values are how we ...
Quick apply
You'll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting. We are diverse in many ways, yet our values unite us. Our values are how we ...
Clinical Research Associate Bridge Program information
See Raleigh, NC salary details
$11.68 - $16.78
0% of jobs
$16.78 - $21.88
8% of jobs
$21.88 - $26.98
13% of jobs
$28.34 is the 25th percentile. Wages below this are outliers.
$26.98 - $32.08
15% of jobs
$32.08 - $37.18
13% of jobs
The median wage is $37.94 / hr.
$37.18 - $42.27
11% of jobs
$42.27 - $47.37
12% of jobs
$49.18 is the 75th percentile. Wages above this are outliers.
$47.37 - $52.47
13% of jobs
$52.47 - $57.57
14% of jobs
$57.57 - $62.67
2% of jobs
$62.67 - $67.77
1% of jobs
$11
$39
$67
How much do clinical research associate bridge program jobs pay per hour?
As of Aug 12, 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?
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 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.
What are popular job titles related to Clinical Research Associate Bridge Program jobs in Raleigh, NC? For Clinical Research Associate Bridge Program jobs in Raleigh, NC, the most frequently searched job titles are:
- Clinical Psychology Research Assistant
- Clinical Research Physician
- Clinical Research Monitor
- Clinical Research Psychiatrist
- Be Well Clinical Studies
- Cra Clinical Research Associate
- Nextstage Clinical Research Llc
- Law School Research Assistant
- Educational Research Assistant
- Clinical Trials Protocol Administrator
What job categories do people searching Clinical Research Associate Bridge Program jobs in Raleigh, NC look for? The top searched job categories for Clinical Research Associate Bridge Program jobs in Raleigh, NC are:
- Clinical Research Assistant
- Remote Clinical Research Coordinator
- Contract Clinical Research
- Full Time Clinical Research Associate
- Research Paramedic
- Entry Level Biotech Clinical Research
- Junior Clinical Research Associate
- Clinical Trials Coordinator
- Full Time Clinical Research Rater
- Clinical Research Project Assistant
What cities near Raleigh, NC are hiring for Clinical Research Associate Bridge Program jobs? Cities near Raleigh, NC with the most Clinical Research Associate Bridge Program job openings:
Parexel rating
8.2
Based on 13 frontline employees who took The Breakroom Quiz
29th of 73 rated research
Job description
Name of Employer: Parexel International LLC
Position Title: Sr. Clinical Research Associate
*Multiple Openings Available*
Position Location: 541 Church at North Hills St., Suite 1000, Raleigh, NC 27609
*100% Remote reporting to Raleigh, NC.
Hours: Full Time / 40 hours per week
Summary of Duties: Engaged in monitoring clinical research that involves understanding human diseases and improving human health. Monitor and oversee clinical trials at client sites. Evaluate quality and integrity of reported data. Represent the company at assigned clinical trial sites and be accountable for quality and delivery from site identification to the close of trial. Conduct, drive, and manage country-specific feasibility and site pre-qualification and qualification activities, which include preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Clinical Site Agreements (CSAs), and any amendments. Conduct on-site and remote visits/contacts, including Qualification, Initiation, Monitoring, Termination Visits, and Site Motivational Visits, and generate site visit reports. Develop strategy to configure, distribute, and collect, review, and approve high-quality country-specific and site-specific documents, essential regulatory documents, and updated or amended regulatory documentation. Customize, review, and negotiate country/site-specific Informed Consent Forms, translations, and customize and negotiate any amendments. Prepare and submit IRB/IEC and MoH/RA applications, resolve conflicts, and determine appropriate follow-up until receipt of final approval. Address and resolve issues at clinical trial sites, including the need for additional training, potential deficiencies in documentation, and communication. Follow-up on Case Report Form data entry, query status, and Serious Adverse Events. Assess and manage test article/study supply including supply, accountability, and destruction/return status. Review and follow-up on site payment status and ensure site receives payments on a timely manner. Communicate study issues that require immediate action with a proposed strategy for resolution. Ensure assigned sites are audit-ready and inspection-ready. Lead and mentor junior CRAs on process/study requirements and perform assessments and co-monitoring visits. Perform report review of visit reports of junior CRAs to ensure compliance with GCP and Protocol Guidelines. Guide Administrative Support Team members, review work, and provide feedback to the manager regarding performance.
Education requirements: Bachelor's degree or equivalent in biological science, pharmaceutical sciences, chemistry, biotechnology, biomedical engineering, or a health-related field of study.
Experience requirements: 3 years of experience in clinical research.
Or, alternatively:
Education requirements : Master's degree or equivalent in biological science, pharmaceutical sciences, chemistry, biotechnology, biomedical engineering, or a health-related field of study.
Experience requirements: 1 year of experience in clinical research.
Special Skills or Other Requirements: Applicants must have demonstrated experience with:
Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management System (CTMS) and Electronic Document Management System (EDMS); Site Management and application of clinical trial methodology and terminology; Independently monitoring visits (Qualification, Site Initiation, and Monitoring); Working with clinical research, phases of clinical trials, current GCP/ICH, and country clinical research law and guidelines; and Communicating results to stakeholders in non-technical language.
Travel requirements: Up to 75% Domestic Travel.
*Position eligible for Employee Referral Program*
To apply: Individuals interested in applying for the position may email a resume with Job #ES2401 to openings@parexel.com
Position Title: Sr. Clinical Research Associate
*Multiple Openings Available*
Position Location: 541 Church at North Hills St., Suite 1000, Raleigh, NC 27609
*100% Remote reporting to Raleigh, NC.
Hours: Full Time / 40 hours per week
Summary of Duties: Engaged in monitoring clinical research that involves understanding human diseases and improving human health. Monitor and oversee clinical trials at client sites. Evaluate quality and integrity of reported data. Represent the company at assigned clinical trial sites and be accountable for quality and delivery from site identification to the close of trial. Conduct, drive, and manage country-specific feasibility and site pre-qualification and qualification activities, which include preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Clinical Site Agreements (CSAs), and any amendments. Conduct on-site and remote visits/contacts, including Qualification, Initiation, Monitoring, Termination Visits, and Site Motivational Visits, and generate site visit reports. Develop strategy to configure, distribute, and collect, review, and approve high-quality country-specific and site-specific documents, essential regulatory documents, and updated or amended regulatory documentation. Customize, review, and negotiate country/site-specific Informed Consent Forms, translations, and customize and negotiate any amendments. Prepare and submit IRB/IEC and MoH/RA applications, resolve conflicts, and determine appropriate follow-up until receipt of final approval. Address and resolve issues at clinical trial sites, including the need for additional training, potential deficiencies in documentation, and communication. Follow-up on Case Report Form data entry, query status, and Serious Adverse Events. Assess and manage test article/study supply including supply, accountability, and destruction/return status. Review and follow-up on site payment status and ensure site receives payments on a timely manner. Communicate study issues that require immediate action with a proposed strategy for resolution. Ensure assigned sites are audit-ready and inspection-ready. Lead and mentor junior CRAs on process/study requirements and perform assessments and co-monitoring visits. Perform report review of visit reports of junior CRAs to ensure compliance with GCP and Protocol Guidelines. Guide Administrative Support Team members, review work, and provide feedback to the manager regarding performance.
Education requirements: Bachelor's degree or equivalent in biological science, pharmaceutical sciences, chemistry, biotechnology, biomedical engineering, or a health-related field of study.
Experience requirements: 3 years of experience in clinical research.
Or, alternatively:
Education requirements : Master's degree or equivalent in biological science, pharmaceutical sciences, chemistry, biotechnology, biomedical engineering, or a health-related field of study.
Experience requirements: 1 year of experience in clinical research.
Special Skills or Other Requirements: Applicants must have demonstrated experience with:
Serving as a Lead Clinical Research Associate (CRA) for clinical studies; Clinical Trial Management System (CTMS) and Electronic Document Management System (EDMS); Site Management and application of clinical trial methodology and terminology; Independently monitoring visits (Qualification, Site Initiation, and Monitoring); Working with clinical research, phases of clinical trials, current GCP/ICH, and country clinical research law and guidelines; and Communicating results to stakeholders in non-technical language.
Travel requirements: Up to 75% Domestic Travel.
*Position eligible for Employee Referral Program*
To apply: Individuals interested in applying for the position may email a resume with Job #ES2401 to openings@parexel.com
About PAREXEL
Sourced by ZipRecruiter
Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.
Industry
Pharmaceutical and medicine manufacturing
Company size
10,000+ Employees
Headquarters location
Waltham, MA, US
Year founded
1983