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Clinical Research Associate Bridge Program Jobs in Brookline, MA

WHOOP

Temporary Clinical Research Associate

Boston, MA · On-site

$52 - $72/hr

As a Temporary Clinical Research Associate , you will provide monitoring and clinical operations support across WHOOP's portfolio of clinical research studies. You will support assigned studies at ...

Whoop

Temporary Clinical Research Associate

Boston, MA · On-site

$45/hr

As a Temporary Clinical Research Associate , you will provide monitoring and clinical operations support across WHOOP's portfolio of clinical research studies. You will support assigned studies at ...

Massgeneralbrigham

Clinical Research Associate

Boston, MA · Remote

$20.16 - $29.01/hr

Working knowledge of clinical research protocols. * Ability to communicate effectively with ... programs designed to celebrate your contributions and support your professional growth. We invite ...

Alira Health Group

Clinical Research Associate

Boston, MA · On-site

$85 - $125/hr

## Clinical Research AssociateApplyremote type: Remotelocations: Boston-Remote: Americas-Remotetime ... The CRA works closely with Lead CRAs, Sr CRAs, in-house CRAs, Associate Director of Clinical ...

New

Alira Health

Clinical Research Associate

Boston, MA · On-site

$85 - $130/hr

The CRA works closely with Lead CRAs, Sr CRAs, in-house CRAs, Associate Director of Clinical ... travel, flexible work programs and more. We welcome your passion and drive, talent and ...

RevBio, Inc.

Clinical Research Manager

Lowell, MA · On-site

The role may include oversight of internal Clinical Research Associates and/or external contract ... Support the development of investigator training strategies, materials, and programs for both ...

Revbio,-Inc.

Clinical Research Manager

Lowell, MA · On-site

$110 - $170/hr

The role may include oversight of internal Clinical Research Associates and/or external contract ... Support the development of investigator training strategies, materials, and programs for both ...

Icon plc

Clinical Research Associate II

Cambridge, MA · 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 ...

Icon plc

Clinical Research Associate II

Boston, MA · 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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All JobsClinical Research Associate Bridge Program JobsClinical Research Associate Bridge Program Jobs in Brookline, MA

Clinical Research Associate Bridge Program information

See Brookline, MA salary details

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$44

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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 Brookline, MA is $44.49, according to ZipRecruiter salary data. Most workers in this role earn between $31.20 and $56.97 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 Brookline, MA look for?

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

Clinical Research Associate Bridge Program jobs near you
Infographic showing various Clinical Research Associate Bridge Program job openings in Brookline, MA as of August 2026, with employment types broken down into 88% Full Time, and 12% Temporary. Highlights an 100% In-person job distribution, with an average salary of $92,549 per year, or $44.5 per hour.

Temporary Clinical Research Associate

WHOOP

Boston, MA • On-site

$52 - $72/hr

Other

Posted 23 days ago

Job description

At WHOOP, we're on a mission to unlock human performance and healthspan. WHOOP empowers members to perform at a higher level through a deeper understanding of their bodies and daily lives.

As a Temporary Clinical Research Associate, you will provide monitoring and clinical operations support across WHOOP’s portfolio of clinical research studies. You will support assigned studies at various stages of the clinical lifecycle, including startup, active study conduct, monitoring, and closeout.

You will conduct monitoring activities, review study documentation, support Trial Master File quality, track study issues, and help ensure that studies are conducted in accordance with approved protocols, Good Clinical Practice, applicable regulations, and WHOOP procedures.

This role requires a detail-oriented and collaborative CRA who can independently manage assigned monitoring activities, communicate effectively with research sites and internal teams, and elevate risks or compliance concerns appropriately. Depending on study timelines and business needs, you may support one or more studies during the contract period.

This is a 6 month, temporary position with an hourly pay rate of $45/hr.

Responsibilities:

  • Conduct remote and onsite monitoring activities for assigned studies, including Site Initiation Visits, Interim Monitoring Visits, Closeout Visits, and other study-specific visits.

  • Perform monitoring activities in accordance with approved protocols, monitoring plans, Good Clinical Practice, applicable regulations, and WHOOP procedures.

  • Review informed consent documentation, participant eligibility, source documentation, case report forms, protocol adherence, safety documentation, and study data for accuracy and completeness.

  • Prepare accurate and timely monitoring visit reports, follow-up communications, action-item trackers, and study status updates.

  • Identify, document, track, and elevate protocol deviations, data quality concerns, safety issues, compliance risks, and operational challenges.

  • Support site readiness activities, including review of essential documents, training completion, systems access, and operational preparedness.

  • Assist with site and study team training on protocols, study procedures, documentation requirements, and clinical systems.

  • Create and maintain assigned study logs, trackers, monitoring templates, and clinical operations documentation.

  • Collaborate with Clinical Operations, Clinical Science, Clinical Research Coordinators, Data Management, Regulatory, Quality, investigators, research sites, and external vendors.

  • Support study closeout activities, including document reconciliation, and action-item resolution, final monitoring activities, and Trial Master File completion.

Qualifications

  • Bachelor’s degree in life sciences, nursing, public health, clinical research, or a related field, or equivalent relevant experience.

  • 3+ years of experience in clinical research, including at least 1 year performing clinical monitoring or CRA responsibilities.

  • Strong attention to detail and the ability to identify and clearly document study risks, compliance concerns, and data quality issues.

  • Strong written communication skills, including the ability to prepare clear monitoring reports and site follow-up correspondence.

Desired:

  • Experience supporting medical-device, digital-health, wearable-technology, or remote-monitoring studies.

  • Familiarity with ISO 14155 or clinical research involving medical devices.

  • Experience working in a sponsor, CRO, or research-site environment.

  • Experience supporting studies related to cardiovascular health, women’s health, sleep, metabolic health, or digital biomarkers.

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About Whoop

Sourced by ZipRecruiter

At WHOOP, we're on a mission to unlock human performance. WHOOP empowers users (Olympians, Professional Athletes, Fitness Enthusiasts, etc) to perform at a higher level through a deeper understanding of their bodies and daily lives.

Industry

Fitness and sports centers

Company size

501 - 1,000 Employees

Headquarters location

Boston, MA, US

Year founded

2012

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