ZipRecruiter

Log In

1

Clinical Research Associate Bridge Program Jobs in Baltimore, MD

Axle

Temporary - Clinical Research Coordinator

Baltimore, MD · On-site

$24 - $32/hr

Axle is seeking a Clinical Research Coordinator (Temporary - Approximately 4 Months) to join our ... Dependent Care Assistant Program (DCAP) * Transportation Reimbursement Account (TRN) Position ...

Axle

Temporary - Clinical Research Coordinator

Baltimore, MD · On-site

$24 - $32/hr

Axle is seeking a Clinical Research Coordinator (Temporary - Approximately 4 Months) to join our ... Dependent Care Assistant Program (DCAP) * Transportation Reimbursement Account (TRN) Position ...

previous pagenext page

Showing results 21-40

All JobsClinical Research Associate Bridge Program JobsClinical Research Associate Bridge Program Jobs in Baltimore, MD

Clinical Research Associate Bridge Program information

See Baltimore, MD salary details

$11

$40

$69

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 Baltimore, MD is $40.86, according to ZipRecruiter salary data. Most workers in this role earn between $28.65 and $52.31 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 are popular job titles related to Clinical Research Associate Bridge Program jobs in Baltimore, MD?

For Clinical Research Associate Bridge Program jobs in Baltimore, MD, the most frequently searched job titles are:

What job categories do people searching Clinical Research Associate Bridge Program jobs in Baltimore, MD look for?

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

Clinical Research Associate Bridge Program jobs near you
Infographic showing various Clinical Research Associate Bridge Program job openings in Baltimore, MD as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, 1% Temporary, and 4% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $84,998 per year, or $40.9 per hour.

Research Associate (Per Diem Overnight Shift)

Parexel

Baltimore, MD • On-site

$20 - $22/hr

Part-time

Medical, Life, Retirement, PTO

Re-posted 17 days ago

Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

34th of 75 rated research

Job description

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

Job Title: Entry level Research Associate (per diem)

Work Location: onsite in Baltimore, MD

Parexel Early Phase Clinical Unitsupports the development of innovative new medicines which are vital for public health, improving outcomes, and saving lives. The early phase and "first in human" trials are the first step in testing these novel treatments in humans.

At Parexel Baltimore, MD unit our highly trained and skilled Research Associates are crucial to ensuring the successful completion of Phase I trials. This is a great role for anyone that aspires to be an enrollment specialist, clinical research coordinator, or eventually manager. Parexel provides a great system of support to help you grow and advance your career internally.

What you'll do after training is completed(including but not limited):

  • You will understand study protocols and be able to complete required medical procedures.

  • Recruit study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments.

  • Enter study participants in the study participant tracking system and study logs, maintain appointment calendars, and operate company information systems and computer programs.

  • Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results.

  • Prepare/monitor study supplies and stock levels in clinic/hospital.

  • Ensure basic study participant safety is provided.

  • Assist with Monitor visits (i.e., room set up, etc.).

  • Maintain and update knowledge of Clinical Operating Guidelines and their proper application.

  • Assume appropriate role with study participants and caregivers.

  • Assure quality and accuracy of source and CRF documentation.

  • Comply with Quality Management (QM) department guidelines and perform corrections for QM, CRC and Monitor/Sponsor Representative in a timely manner.

Your Profile:

  • Proven customer service experience in a fast-paced environment

  • Background working in a medical or clinical setting

  • Comfortable with prolonged periods of standing and walking

  • B.S.+ in related life science field OR HS diploma/GED with relevant experience

  • CPT/Phlebotomy is highly preferred

Hours/Shift - please note this is not a full-time opportunity we are currently seeking per diem candidates (this role is not eligible for full time benefits)

Required Training: First 4 to 6 weeks required to work 40 hours a week for training (day shift - 6:50am to 3:20pm)

After training is completed:

  • Minimum availability requirements: two 12 hour overnight shifts weekly as well as two 12-hour weekend shifts in a 4-week month OR three 12-hour weekend shifts in a 5-week month

  • The actual number of hours scheduled and confirmed can vary between 0-40 hours a week, depending on business needs (hours are not guaranteed)

  • Shift Details: overnight start usually around 7pm

  • Bi-monthly attendance may be required for training sessions, unless there are no mandatory trainings to complete

Base Pay Range: $20.00 to $22.00 per hour eligible for shift differentials

Actual salaries may vary within the range based on several factors including, but not limited to education, training, experience, professional achievement, and location.

In addition to base salary, some roles may be eligible for participation in Parexel's annual performance-based bonus plan, annual salary review and additional total rewards incentives.

Our talent acquisition team will provide additional details on our bonus plan or incentive programs for those eligible roles. For all eligible employees, we offer market leading benefit programs including paid time off, 401k match, life insurance, health insurance, and other benefit offerings in accordance with the terms of applicable plans.

EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

What Parexel employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

PAREXEL logo

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

View All PAREXEL Jobs

Apply