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Temporary Clinical Research Scientist 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 ... Collaborate with Clinical Operations, Clinical Science, Clinical Research Associates, Data ...

New

InStride Health

Clinical Research Scientist

$106K - $118K/yr

The Clinical Research Scientist will play a key role in clinical outcomes evaluation within a highly collaborative, cross-functional environment. The individual will work closely with clinical ...

Axle

Temporary - Clinical Research Coordinator

Baltimore, MD · On-site

$24 - $32/hr

With experts in biomedical science, software engineering, and program management, we focus on ... Axle is seeking a Clinical Research Coordinator (Temporary - Approximately 4 Months) to join our ...

Whoop

Temporary Clinical Research Associate

Boston, MA · On-site

$45/hr

As a Temporary Clinical Research Associate , you will provide monitoring and clinical operations ... Collaborate with Clinical Operations, Clinical Science, Clinical Research Coordinators, Data ...

New

Uofl

$23.25 - $31/hr

Health Sciences Center Time Type: Part time Worker Type: Temporary (Fixed Term) Job Req ID: R109013 ... A Temporary Clinical Research Coordinator is needed to coordinate clinical research studies ...

Promedica

Clinical Research Scientist

Toledo, OH

As the Clinical Research Scientist, you implement investigator-initiated clinical research studies through collaboration with physicians, researchers, and research staff. You will develop hypotheses ...

Zipongo

Clinical Research Scientist

San Francisco, CA · On-site

We are looking for an outstanding Clinical Research Scientist with strong human subjects research and statistics experience (nutritional epidemiology preferred) to evaluate and improve our Foodsmart ...

Zipongo

Clinical Research Scientist

San Francisco, CA · On-site

We are looking for an outstanding Clinical Research Scientist with strong human subjects research and statistics experience (nutritional epidemiology preferred) to evaluate and improve our Foodsmart ...

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

As of Aug 12, 2026, the average hourly pay for temporary clinical research scientist in the United States is $56.32, according to ZipRecruiter salary data. Most workers in this role earn between $43.99 and $67.31 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a temporary clinical research scientist?

To thrive as a Temporary Clinical Research Scientist, you need a solid background in life sciences or a related field, experience in clinical research methodologies, and often an advanced degree such as a PhD or PharmD. Familiarity with regulatory guidelines (like GCP), data management systems, and statistical analysis software (such as SAS or SPSS) is crucial. Excellent organizational, analytical, and communication skills help manage projects efficiently and collaborate with diverse teams. These competencies ensure rigorous study execution, regulatory compliance, and the generation of reliable research outcomes within limited assignment timeframes.

What does a temporary clinical research scientist do?

A Temporary Clinical Research Scientist assists in designing, conducting, and analyzing clinical trials or research studies for a set period. Their responsibilities may include collecting and managing data, ensuring regulatory compliance, and collaborating with medical staff and other scientists. These professionals help ensure that studies are conducted safely, ethically, and according to protocol. Because the position is temporary, it often supports ongoing projects that require additional expertise or staffing for a limited time.

What is the difference between Temporary Clinical Research Scientist vs Clinical Research Associate?

AspectTemporary Clinical Research ScientistClinical Research Associate
CredentialsBachelor's or Master's in Life Sciences, relevant certificationsBachelor's or Master's in Life Sciences, often with GCP training
Work EnvironmentResearch labs, pharmaceutical companies, CROsMonitoring clinical trials at sites, data review
Employer & Industry UsagePharmaceutical companies, biotech firms, CROsPharmaceutical companies, CROs, clinical trial sites

The main difference is that a Temporary Clinical Research Scientist typically conducts research and data analysis in labs or research settings, while a Clinical Research Associate primarily monitors clinical trial sites and ensures compliance. Both roles require relevant scientific credentials and are common in the pharmaceutical and biotech industries, but they focus on different aspects of clinical research.

What cities are hiring for Temporary Clinical Research Scientist jobs? Cities with the most Temporary Clinical Research Scientist job openings:
What are the most commonly searched types of Clinical Research Scientist jobs? The most popular types of Clinical Research Scientist jobs are:
What states have the most Temporary Clinical Research Scientist jobs? States with the most job openings for Temporary Clinical Research Scientist jobs include:
Temporary Clinical Research Scientist jobs near you

Temporary Clinical Research Coordinator

Whoop

Boston, MA • On-site

$34/hr

Full-time

Posted yesterday

New

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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