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Temporary H1B Clinical Research Jobs (NOW HIRING)

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 ...

Guidehouse

Clinical Research Coordinator

Bethesda, MD · On-site

$65K - $108K/yr

Provide guidance and operational training to junior staff, trainees, students, and temporary personnel as requested by the Government. * Coordinate multiple clinical research studies simultaneously ...

Guidehouse

Clinical Research Coordinator

Bethesda, MD · On-site

$65K - $108K/yr

Provide guidance and operational training to junior staff, trainees, students, and temporary personnel as requested by the Government. * Coordinate multiple clinical research studies simultaneously ...

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How much do temporary h1b clinical research jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for temporary h1b clinical research in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What is the difference between Temporary H1B Clinical Research vs Temporary H1B Clinical Data Coordinator?

AspectTemporary H1B Clinical ResearchTemporary H1B Clinical Data Coordinator
Required CredentialsBachelor's degree in life sciences or related field, relevant certificationsBachelor's degree, often in health informatics or related field, certifications may vary
Work EnvironmentResearch sites, hospitals, pharmaceutical companiesData management departments, clinical research organizations
Employer & Industry UsagePharmaceutical, biotech, CROsPharmaceutical companies, CROs, research institutions

Temporary H1B Clinical Research roles focus on overseeing clinical trials, while Temporary H1B Clinical Data Coordinators handle data collection and management. Both roles require relevant degrees and certifications, but their daily tasks and work environments differ, reflecting their distinct responsibilities within the clinical research process.

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Temporary H1B Clinical Research jobs near you
Infographic showing various Temporary H1B Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Temporary Clinical Research Associate

Whoop

Boston, MA • On-site

$45/hr

Full-time

Posted 28 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 escalate 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 escalate 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, 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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