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Temporary Weekend Clinical Research Jobs (NOW HIRING)

Whoop

Temporary Clinical Research Coordinator

Boston, MA · On-site

$34/hr

As a Temporary Clinical Research Coordinator , you will provide hands-on operational support across WHOOP's portfolio of clinical research studies. You will support assigned studies at various stages ...

Axle

Temporary - Clinical Research Coordinator

Baltimore, MD · On-site

$24 - $32/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Axle is seeking a Clinical Research Coordinator (Temporary - Approximately 4 Months) to join our vibrant team at the National Institutes of Health (NIH) in Baltimore, MD. This position will support ...

Axle

Temporary - Clinical Research Coordinator

Baltimore, MD · On-site

$24 - $32/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Axle is seeking a Clinical Research Coordinator (Temporary - Approximately 4 Months) to join our vibrant team at the National Institutes of Health (NIH) in Baltimore, MD. This position will support ...

Uofl

$23.25 - $31/hr

A Temporary Clinical Research Coordinator is needed to coordinate clinical research studies conducted at the Department of Surgery, Division of Surgical Oncology. Clinical Research at the Department ...

Flourish Research

Clinical Research Coordinator

Murrieta, CA

$31 - $38/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Valkyrie Clinical Trials, a Flourish Research company, is looking for motivated, talented, creative ... Monday-Friday, 8:30 AM - 5 PM (occasional weekends) Location: 25405 Hancock Ave, Suite 110 ...

Flourish Research

Clinical Research Coordinator

Murrieta, CA · On-site

$31 - $38/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Valkyrie Clinical Trials, a Flourish Research company, is looking for motivated, talented, creative ... Monday-Friday, 8:30 AM - 5 PM (occasional weekends) Location: 25405 Hancock Ave, Suite 110 ...

Flourish Research

Clinical Research Coordinator

Murrieta, CA · On-site

$31 - $38/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Valkyrie Clinical Trials, a Flourish Research company, is looking for motivated, talented, creative ... Monday-Friday, 8:30 AM - 5 PM (occasional weekends) Location: 25405 Hancock Ave, Suite 110 ...

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Temporary Weekend Clinical Research information

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

As of Aug 15, 2026, the average hourly pay for temporary weekend 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 Weekend Clinical Research vs Temporary Weekend Clinical Data Coordinator?

AspectTemporary Weekend Clinical ResearchTemporary Weekend Clinical Data Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; some roles may need clinical research certificationsRequires a bachelor's degree in health informatics, data management, or related field; certifications like CDMP are a plus
Work EnvironmentResearch sites, hospitals, or clinics conducting clinical trialsData management departments within research organizations or hospitals
Employer & Industry UsagePharmaceutical companies, CROs, academic research institutionsResearch organizations, hospitals, clinical trial sponsors

Temporary Weekend Clinical Research involves assisting with clinical trials, patient interactions, and trial procedures during weekends. In contrast, Temporary Weekend Clinical Data Coordinators focus on managing and ensuring the accuracy of trial data. Both roles often require similar educational backgrounds but differ in daily responsibilities and focus areas within the clinical research industry.

What cities are hiring for Temporary Weekend Clinical Research jobs?

Cities with the most Temporary Weekend Clinical Research job openings:

What are the most commonly searched types of Weekend Clinical Research jobs?

The most popular types of Weekend Clinical Research jobs are:

What states have the most Temporary Weekend Clinical Research jobs?

States with the most job openings for Temporary Weekend Clinical Research jobs include:

Temporary Weekend Clinical Research jobs near you

Temporary Clinical Research Coordinator

Whoop

Boston, MA • On-site

$34/hr

Full-time

Posted 4 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 Coordinator, you will provide hands-on operational support across WHOOP's portfolio of clinical research studies. You will support assigned studies at various stages of the clinical lifecycle, including startup, participant recruitment and enrollment, active study conduct, data collection, and closeout.
You will coordinate day-to-day study activities, support participants and research sites, maintain study documentation and tracking tools, and help ensure that study procedures are completed accurately and on time. You may support one or more studies based on program timelines and business needs.
This role requires a highly organized and detail-oriented coordinator who can manage multiple priorities, communicate clearly with participants and study teams, and follow established protocols and processes. The ideal candidate is comfortable working in a fast-paced environment and using clinical research systems to support high-quality study execution.
This is a 6 month, temporary position with an hourly pay rate of $34/hr.
Responsibilities:
  • Support study startup activities, including development and maintenance of study workflows, checklists, logs, trackers, training materials, and participant-facing documents.
  • Assist with the configuration, testing, and operational readiness of study systems, including electronic data capture, participant management, scheduling, and compensation platforms.
  • Support participant recruitment, prescreening, scheduling, informed consent coordination, enrollment, and study visit preparation in accordance with approved study procedures.
  • Review study documentation for completeness and follow up on missing, inconsistent, or incomplete information.
  • Support the resolution of data queries, documentation discrepancies, and outstanding study action items.
  • Maintain participant enrollment logs, screening logs, visit trackers, delegation logs, training logs, device accountability records, compensation trackers, and other study documentation.
  • Assist with study team and site training by coordinating meetings, preparing materials, tracking attendance, and documenting completion.
  • Identify and promptly escalate participant concerns, protocol deviations, safety information, data quality concerns, and operational risks to the appropriate study team member.
  • Collaborate with Clinical Operations, Clinical Science, Clinical Research Associates, Data Management, Regulatory, Quality, investigators, research sites, vendors, and other cross-functional partners.
  • Support the collection, filing, and quality review of study documents within the Trial Master File or other study repositories.
  • Assist with study closeout activities, including participant follow-up, document reconciliation, device and supply reconciliation, outstanding data resolution, and archive preparation.
  • Contribute feedback and lessons learned to help improve study workflows and Clinical Operations processes.
Qualifications:
  • Bachelor's degree in life sciences, public health, psychology, nursing, clinical research, or a related field, or equivalent relevant experience.
  • 2+ years of experience supporting clinical research, healthcare research, academic research, or human-subject studies.
  • At least 1 year of experience performing clinical research coordination, participant-facing research, or similar study operations responsibilities.
  • Working knowledge of Good Clinical Practice and applicable human-subject research requirements.
  • Strong organizational and time-management skills, with the ability to manage multiple participants, assignments, and deadlines.
  • Strong attention to detail and commitment to accurate, complete, and timely documentation.
  • Excellent written and verbal communication skills, including the ability to communicate professionally and empathetically with research participants.
Desired:
  • Experience supporting medical-device, digital-health, wearable-technology, or remote-monitoring studies.
  • Experience working directly with research participants in decentralized, virtual, hybrid, or site-based studies.
  • Familiarity with FDA-regulated clinical research or ISO 14155.
  • Experience supporting studies related to cardiovascular health, women's health, sleep, metabolic health, or digital biomarkers.
  • Experience working in a sponsor, CRO, academic research center, hospital, or clinical research site.
Whoop logo

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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