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Temporary Clinical Research Assistant Jobs (NOW HIRING)

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 ... Dependent Care Assistant Program (DCAP) * Transportation Reimbursement Account (TRN) Position ...

Uofl

$23.25 - $31/hr

A Temporary Clinical Research Coordinator is needed to coordinate clinical research studies ... * Assist in enhancing recruitment of study participants, helping with the design and ...

Headlands Research

Clinical Research Assistant

Maplewood, MN · On-site

$18 - $27/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We're seeking a Clinical Research Assistant for our clinical research site located in Maplewood, MN. Type: Regular Full-time Employee Schedule: Mondays through Fridays, 8:00am - 5:00pm Pay Range: $18 ...

Whoop

Temporary Clinical Research Associate

Boston, MA · On-site

$45/hr

As a Temporary Clinical Research Associate , you will provide monitoring and clinical operations ... * Assist with site and study team training on protocols, study procedures, documentation ...

Actalent

Clinical Research Assistant

Artesia, CA · On-site

$20 - $25/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Title: Clinical Research Assistant/Phlebotomist $20-25/hr --with TONS of career growth ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

ALLIANCE CLINICAL LLC

Clinical Research Assistant

Rochester, NY · On-site

$20 - $22/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Summary: The Clinical Research Assistant supports the conduct of clinical trials by performing protocol-required procedures, coordinating study activities, and engaging directly with study ...

Headlands Research

Clinical Research Assistant

Maplewood, MN · On-site

$18 - $27/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

We're seeking a Clinical Research Assistant for our clinical research site located in Maplewood, MN. Type: Regular Full-time Employee Schedule: Mondays through Fridays, 8:00am - 5:00pm Pay Range: $18 ...

Prism Vision Group

Clinical Research Assistant

Fairfax, VA · On-site

$46K - $96K/yr

The Clinical Research Assistant will perform a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data. The Clinical Research Assistant will ...

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 ... Dependent Care Assistant Program (DCAP) * Transportation Reimbursement Account (TRN) Position ...

One GI, LLC

Clinical Research Assistant

Mentor, OH

$17 - $22/hr

  • Retirement

  • PTO

Clinical Research Assistant Be Part of Research That Makes a Difference Are you detail-oriented, organized, and passionate about advancing patient care through clinical research? Join our team as a ...

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Temporary Clinical Research Assistant information

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

As of Aug 16, 2026, the average hourly pay for temporary clinical research assistant in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What is a temporary clinical research assistant?

Temporary Clinical Research Assistants are professionals hired for a limited period to support clinical research studies. They typically assist with tasks such as data collection, participant recruitment, sample processing, and maintaining accurate study records. These roles are crucial for ensuring the smooth operation of clinical trials and may require working under the supervision of a principal investigator or research coordinator. Temporary positions are often used to meet short-term project needs or to provide extra help during busy periods.

What are the typical responsibilities of a temporary clinical research assistant and how do they support the research team?

As a Temporary Clinical Research Assistant, you'll be involved in supporting ongoing clinical trials by handling tasks such as data entry, patient recruitment, scheduling study visits, and collecting or processing samples. You'll work closely with study coordinators, principal investigators, and sometimes with participants to ensure research protocols are followed accurately and ethically. The role often requires strong organizational skills and attention to detail, as well as adaptability to shifting priorities. Your support is crucial to maintaining the integrity and smooth operation of clinical research projects.

What are the key skills and qualifications needed to thrive as a temporary clinical research assistant, and why are they important?

To thrive as a Temporary Clinical Research Assistant, you need a background in life sciences, attention to detail, and familiarity with research methodologies, often supported by a bachelor’s degree or equivalent experience. Competence in data entry systems, spreadsheets, and understanding of Good Clinical Practice (GCP) guidelines is typically required. Strong organizational skills, effective communication, and the ability to work independently help candidates stand out in this role. These skills are crucial for ensuring accurate data collection, regulatory compliance, and the smooth execution of clinical studies.

What is the difference between Temporary Clinical Research Assistant vs Clinical Research Coordinator?

AspectTemporary Clinical Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRA are a plusUsually requires a bachelor's degree; certifications like CCRP or CCRC are common
Work EnvironmentAssists in clinical trial activities, often in research labs or hospitals, on a temporary basisManages entire clinical trial processes, often in hospital or research settings, with ongoing responsibilities
Employer & Industry UsageUsed by research institutions, hospitals, and pharmaceutical companies for short-term rolesEmployed by research sites, hospitals, and CROs for long-term or project-based roles

The main difference is that a Temporary Clinical Research Assistant typically works on short-term projects assisting with specific research tasks, while a Clinical Research Coordinator manages the overall conduct of clinical trials, often in a permanent or long-term capacity. Both roles require similar educational backgrounds and certifications but differ in scope and duration of employment.

What cities are hiring for Temporary Clinical Research Assistant jobs?

Cities with the most Temporary Clinical Research Assistant job openings:

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

The most popular types of Temporary Clinical Research jobs are:

What states have the most Temporary Clinical Research Assistant jobs?

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

Temporary Clinical Research Assistant jobs near you

Temporary - Clinical Research Coordinator

Axle

Baltimore, MD • On-site

$24 - $32/hr

Temporary

Medical, Dental, Vision, Retirement, PTO

Re-posted yesterday

Job description

(ID: 2026-2380)
Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad. With experts in biomedical science, software engineering, and program management, we focus on developing and applying research tools and techniques to empower decision-making and accelerate research discoveries. We work with some of the top research organizations and facilities in the country including multiple institutes at the National Institutes of Health (NIH).
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 ongoing clinical research activities within the National Institute on Drug Abuse (NIDA) and offers an opportunity to contribute to cutting-edge behavioral and clinical research initiatives.
Benefits We Offer:
  • 100% Medical, Dental & Vision Coverage for Employees
  • Paid Time Off and Paid Holidays
  • 401K match up to 5%
  • Educational Benefits for Career Growth
  • Employee Referral Bonus
  • Flexible Spending Accounts:
    • Healthcare (FSA)
    • Parking Reimbursement Account (PRK)
    • Dependent Care Assistant Program (DCAP)
    • Transportation Reimbursement Account (TRN)

Position Information:
Under this task order, the contractor will independently provide support services to satisfy the overall operational objectives of the National Institute on Drug Abuse. The primary objective is to provide services and deliverables through performance of support services.
Additional Qualifications
Certifications & Licenses:
  • Minimum of one (1) year of experience in behavioral counseling, preferably in drug/smoking/alcohol treatment.
  • Minimum of three (3) years of experience in a research related field.
  • Master's degree in psychology, social work, biological sciences or related discipline.
  • Basic Life Support (BLS) certification will be required - training will be provided.

Field of Study:
  • Social Work (Required)

Software:
  • Proficient computer skills required (e.g. Microsoft Office)

Skills:
  • Will complete all NIH/NIDA Mandatory trainings or/and other required trainings by the deadline set forth.
  • Excellent analytical, organizational and time management skills required.
  • Strong communications skills, both oral and written.
  • Exceptional interpersonal skills, customer service oriented and client focused approach to work due to extensive participant contact.
  • Previous experience in human subjects' interaction (clinical or research).
  • Previous clinical trial work

Deliverables:
  • Work products and documents related to administering mental health assessments and diagnostic interviews. - Ad-Hoc
  • Work products and documents related to obtaining participant medical and drug use information according to protocol criteria. - Ad-Hoc
  • Work products and documents related to obtaining informed consent documentation from participants in the screening protocol. - Ad-Hoc
  • Work products and documents related to follow-up correspondence to candidates on recruiting status. - Ad-Hoc
  • Work products and documents related to arranging travel and distributing remuneration for candidates. - Ad-Hoc
  • Work products and documents related to scheduling phone screen scripts, in person screening appointments and communications with candidates. - Ad-Hoc
  • Work products and documents related to data entry in the electronic medical record system., generating reports; perform study procedures; process and destroy specimens as needed; maintain storage records/inventory of biological specimens. - Ad-Hoc

Statement of Work Details:
  • Assist preparing and submitting for review accurate source documents related to all research procedures . - 1
  • Participate in developing and maintaining research protocol documentation and operations. - 2
  • Assist researchers with study testing, observations data entry and other duties associated with study sessions. - 3
  • Supports clinical staff develop, implement and maintain clinical research data files and materials.
  • Acquaint participants with the MRI or mock MRI scanner to assess their comfort level, fit and eligibility to participate in MRI studies.
  • Collects research data and prepares information for inputs and analysis.
  • Verify study participant information and collect data and results of testing.
  • Assist staff develop, assemble related documentation and maintain regulatory binders for all protocols.
  • Perform accurate and timely data analysis, report results and findings and respond to sponsor queries.
  • Set up, format and enter data into spreadsheets to analyze information and create reports.
  • Enter data into research databases, systems and applications for ongoing studies.
  • Supports the development of forms and questionnaires.
  • Assist researchers develop, maintain and complete study data collection forms and source documents.
  • Review draft protocols, case report forms, and manuals of operations for clarity, and completeness.
  • Work with staff on the design, development and preparation of documents such as spreadsheets, letters, rosters, agendas, presentations and meeting minutes summaries.
  • Supports the collection of data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.
  • Assist staff screen prospective study subjects and participate in scheduling participants for research visits and procedures.
  • Schedule and coordinate outpatient and inpatient visits, diagnostic studies and medical tests.
  • Assist researchers with the collection and analysis of research data and samples.
  • Monitors subject's progress and reports adverse events.
  • Liaison between the study subjects and the investigators concerning any problems or adverse events including out of range vitals, etc.
  • Supports assembly, development and review of new research projects.
  • Assist key research personnel ensure that clinical research activities are performed in accordance with federal, state and institutional regulations, policies and procedures.
  • Assist researchers plan and coordinate the initiation of research study protocol and the implementation of operating policies and procedures.
  • Assist researchers develop and maintain current and new research protocols.
  • Supports the creation and management of clinical websites and web-based tools.
  • Collaborate with information technology IT staff to perform updates to a variety of websites.
  • Organizes and performs clinical research, utilizing internet and other available clinical resources.
  • Maintain and organize an online resource of documentation regarding clinical trials, including Standard Operating Procedure documents for all tasks related to the handling of clinical trials.
  • Provides assistance to staff in the collection, development and quality control of essential clinical research efforts.
  • Assist staff on all facets of clinical studies including subject enrollment, scheduling outpatient appointments and inpatient admissions, travel arrangements, investigation consent, subject longitudinal monitoring, study data, sample collection and data entry.
  • Supports clinical staff develop, implement and maintain clinical research data files and materials.
  • Prepare and submit for review accurate source documents related to all research procedures.
  • Develop and maintain research protocol documentation and operations.
  • Develops and facilitates training to new research coordinators and mentors researchers in Good Clinical Practices.
  • Instruct data entry and clinical staff in procedures relative to data management, protocol instructions, Standard Operating Procedures and regulatory processes and considerations.
  • Organize, prepare and distribute informational materials and provide support to the educational mission of the study.
  • Prepare materials, coordinate scheduling, track attendance and report results of workshops related research best practices, emerging trends in clinical studies, new literature and findings and regulatory considerations.
  • Mentor new clinical research coordinators on all aspects of research support.

Disclaimer: The above description is meant to illustrate the general nature of work and level of effort being performed by individuals assigned to this position or job description. This is not restricted as a complete list of all skills, responsibilities, duties, and/or assignments required. Individuals may be required to perform duties outside of their position, job description or responsibilities as needed.
The diversity of Axle's employees is a tremendous asset. We are firmly committed to providing equal opportunity in all aspects of employment and will not tolerate any illegal discrimination or harassment based on age, race, gender, religion, national origin, disability, marital status, covered veteran status, sexual orientation, status with respect to public assistance, and other characteristics protected under state, federal, or local law and to deter those who aid, abet, or induce discrimination or coerce others to discriminate.
Accessibility: If you need an accommodation as part of the employment process please contact: careers@axleinfo.com
This role has a market-competitive salary with an anticipated base compensation range listed below. Actual salaries will vary depending on a candidate's experience, qualifications, skills, and location.
Salary Range
$60-$64 USD

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