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Temporary Clinical Research Protocol Writer Jobs

Uofl

$23.25 - $31/hr

A Temporary Clinical Research Coordinator is needed to coordinate clinical research studies ... Facilitates compliance with the research protocol and Good Clinical Practice guidelines. * Uses ...

Whoop

Temporary Clinical Research Associate

Boston, MA · On-site

$45/hr

Perform monitoring activities in accordance with approved protocols, monitoring plans, Good ... Strong written communication skills, including the ability to prepare clear monitoring reports and ...

Axle

Temporary - Clinical Research Coordinator

Baltimore, MD · On-site

$24 - $32/hr

Strong communications skills, both oral and written. * Exceptional interpersonal skills, customer ... Review draft protocols, case report forms, and manuals of operations for clarity, and completeness.

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Temporary Clinical Research Protocol Writer information

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$54

$83

How much do temporary clinical research protocol writer jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for temporary clinical research protocol writer in the United States is $54.35, according to ZipRecruiter salary data. Most workers in this role earn between $39.90 and $64.18 per hour, depending on experience, location, and employer.

What is the difference between Temporary Clinical Research Protocol Writer vs Temporary Clinical Research Associate?

AspectTemporary Clinical Research Protocol WriterTemporary Clinical Research Associate
Primary RoleDevelops and writes clinical research protocols and related documentsMonitors and manages clinical trial activities at sites
Required SkillsScientific writing, regulatory knowledge, protocol developmentSite management, data collection, compliance monitoring
Work EnvironmentOffice-based, collaboration with research teamsSite visits, on-site monitoring, coordination with sites
Common CertificationsGCP training, clinical research certificationsGCP training, clinical research certifications

While both roles support clinical trials, the Temporary Clinical Research Protocol Writer focuses on creating detailed protocols and documentation, whereas the Temporary Clinical Research Associate manages trial execution and site activities. Understanding these differences helps in choosing the right position based on skills and career goals.

What cities are hiring for Temporary Clinical Research Protocol Writer jobs?

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Temporary Clinical Research Protocol Writer jobs near you

Temporary Clinical Research Coordinator

Whoop

Boston, MA • On-site

$34/hr

Full-time

Posted 5 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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