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Temporary Clinical Research Jobs (NOW HIRING)

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

$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 ...

Actalent

Clinical Research Nurse

Mobile, AL

$35 - $42/hr

Job Title: Clinical Research Nurse (Oncology) - Part-Time, Mobile, AL This part-time Clinical ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

Actalent

Clinical Research Nurse

Mobile, AL · On-site

$35 - $42/hr

Clinical Research Nurse (Oncology) This part-time Clinical Research Nurse position supports an ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

Actalent

Clinical Research Coordinator

Richmond, TX

$25 - $35/hr

Job Title: Bilingual Clinical Research Coordinator Hours: 40 hours per week Contract Position ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

New

Tekberry

Clinical Research Coordinator

Stanford, CA · On-site

$44 - $51/hr

Clinical Research Coordinator Pay Rate Range: $44.00 - $51.00/hr. (W2) (DOE) Employment Type ... Contract (Potential Temp-to-Hire) Duration: Approximately 6 Months (Potential Extension/Conversion ...

A.P.R., Inc. (AlphaProTemps)

Be Seen First

Clinical Research Coordinator (CRC)

Kalamazoo, MI · On-site

$44/hr

3 - 6 Month Contract Potential (Temp-to-Hire) Fully Onsite Monday - Friday 8:00 am - 5:00 pm M-F ... Research documents * Clinical trial documents * Operating and maintenance instructions * Procedure ...

Actalent

Clinical Research Coordinator

Philadelphia, PA · Hybrid

$30 - $35/hr

Senior Clinical Research Coordinator We are seeking a dedicated Senior Clinical Research ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

Actalent

Clinical Research Nurse

Philadelphia, PA · Hybrid

$35 - $46/hr

Clinical Research Nurse We are seeking a Clinical Research Nurse to support clinical research ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

Actalent

Clinical Research Coordinator

Philadelphia, PA · Hybrid

$30 - $35/hr

Senior Clinical Research Coordinator We are seeking a dedicated Senior Clinical Research ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

Actalent

Clinical Research Nurse

Philadelphia, PA · Hybrid

$35 - $46/hr

Clinical Research Nurse We are seeking a Clinical Research Nurse to support clinical research ... If eligible, the benefits available for this temporary role may include the following: * Medical ...

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Temporary Clinical Research information

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How much do temporary clinical research jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for temporary 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 are the key skills and qualifications needed to thrive in temporary clinical research, and why are they important?

To excel in Temporary Clinical Research, candidates typically need a background in life sciences or healthcare, familiarity with clinical trial protocols, and attention to regulatory compliance. Experience with data collection software, electronic data capture (EDC) systems, and Good Clinical Practice (GCP) certification are highly valuable. Strong organizational, communication, and problem-solving skills help professionals adapt quickly and contribute effectively in temporary project-based settings. These abilities ensure accurate, ethical research conduct and seamless integration with research teams, even on short-term assignments.

What is a temporary clinical research?

A Temporary Clinical Research job involves assisting in medical or scientific studies for a limited period. Responsibilities may include data collection, patient interaction, regulatory compliance, and administrative support. These roles are often project-based and may be available in hospitals, universities, or pharmaceutical companies. Temporary positions allow professionals to gain experience in clinical research without committing to a long-term role.

What are the typical responsibilities of someone working in temporary clinical research?

In a Temporary Clinical Research role, you can expect to assist with tasks such as collecting and managing study data, coordinating participant visits, and ensuring compliance with study protocols. You may also help with regulatory documentation, support the recruitment of research subjects, and collaborate closely with investigators, sponsors, and other research team members. Since these positions are project-based, you’ll need to adapt quickly to new environments and processes. This role provides valuable hands-on experience in clinical research, and can be a great stepping stone for those aiming to advance to permanent or higher-level positions in the field.

More about Temporary Clinical Research jobs
What cities are hiring for Temporary Clinical Research jobs? Cities with the most Temporary Clinical Research job openings:
What are the most commonly searched types of Clinical Research jobs? The most popular types of Clinical Research jobs are:
What states have the most Temporary Clinical Research jobs? States with the most job openings for Temporary Clinical Research jobs include:
What job categories do people searching Temporary Clinical Research jobs look for? The top searched job categories for Temporary Clinical Research jobs are:
Temporary Clinical Research jobs near you
Infographic showing various Temporary Clinical Research job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Coordinator

Guidehouse

Bethesda, MD • On-site

$65K - $108K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 23 days ago

Guidehouse rating

7.7

Company rating: 7.7 out of 10

Based on 27 frontline employees who took The Breakroom Quiz

42nd of 72 rated business consultants

Job description

Job Family:
Clinical Trial Operations
Travel Required:
None
Clearance Required:
Ability to Obtain Public Trust
What You Will Do:
We are seeking a Clinical Research Coordinator to provide comprehensive clinical research coordination services for oncology and cancer-related clinical trials conducted within the National Cancer Institute (NCI). This is a full-time, on-site role in Bethesda, MD.
  • Provide guidance and operational training to junior staff, trainees, students, and temporary personnel as requested by the Government.
  • Coordinate multiple clinical research studies simultaneously.
  • Assist with onboarding activities related to protocol operations and study procedures.
  • Support continuity of operations and knowledge transfer efforts.
  • Collaborate with data management personnel to ensure data quality and completeness.
  • Collect, review, validate, extract, and enter research data into approved electronic systems for analysis, including data from patient charts, medical records, interviews, questionnaires, and diagnostic tests.
  • Support informed consent activities for observational and interventional studies as authorized by the principal investigator (PI).
  • Screen, recruit, pre-screen, and schedule research participants according to protocol requirements.
  • Educate participants regarding protocol requirements, study procedures, investigational therapies, visit schedules, and participant responsibilities.
  • Serve as a primary point of contact for study participants and families.
  • Ensure protocol-required events are completed within protocol-defined visit windows; document participant encounters in the electronic medical record and other approved systems and maintain complete and accurate source documentation.
  • Participate in quality improvement initiatives related to documentation practices.
  • Monitor study participant's progress and report adverse events.
  • Assist with adverse event reporting and protocol deviation documentation.
  • Assist with preparation and submission of regulatory documentation to Institutional Review Boards (IRBs), protocol support offices, sponsors, and regulatory authorities; track regulatory deadlines and submission requirements.
  • Ensure study records remain inspection-ready and audit-ready by maintaining regulatory binders, study files, delegation-of-authority logs, and associated study documentation; support audit preparation and inspection readiness activities.
  • Support compliance with federal regulations governing human subjects' research.
  • Help staff in the collection, development, and quality control of essential clinical research efforts.
  • Ensure protocol conduct complies with National Cancer Institute (NCI), National Institutes of Health (NIH), Food and Drug Administration (FDA), International Council for Harmonization-Good Clinical Practice (ICH-GCP), and applicable regulatory requirements.
  • Coordinate the receipt and distribution of study materials and maintain accountability records for study resources.
  • Support clinical staff in developing, implementing, and maintaining clinical research data files and materials.

What You Will Need:
  • Bachelor's degree in nursing, health sciences, public health, clinical research, or related field
  • Minimum of ONE (1) year of experience supporting clinical trials from startup through closeout.
  • Experience supporting oncology clinical trials and clinical research operations.
  • Knowledge of FDA regulations ICH-GCP, human subjects protection, and clinical trial methodology.
  • Experience with electronic medical records, clinical trial management systems, and electronic data capture platforms.
  • Must be able to obtain and maintain a Federal or DoD "public trust"; candidates must receive approved adjudication prior to onboarding with Guidehouse. Candidates with an active public trust or suitability are preferred.

What Would Be Nice To Have:
  • Strong organizational and project coordination skills
  • Effective communication skills

The annual salary range for this position is $65,000.00-$108,000.00. Compensation decisions depend on a wide range of factors, including but not limited to skill sets, experience and training, security clearances, licensure and certifications, and other business and organizational needs.
What We Offer:
Guidehouse offers a comprehensive, total rewards package that includes competitive compensation and a flexible benefits package that reflects our commitment to creating a diverse and supportive workplace.
Benefits include:
  • Medical, Rx, Dental & Vision Insurance
  • Personal and Family Sick Time & Company Paid Holidays
  • Parental Leave
  • 401(k) Retirement Plan
  • Group Term Life and Travel Assistance
  • Voluntary Life and AD&D Insurance
  • Health Savings Account, Health Care & Dependent Care Flexible Spending Accounts
  • Transit and Parking Commuter Benefits
  • Short-Term & Long-Term Disability
  • Tuition Reimbursement, Personal Development, Certifications & Learning Opportunities
  • Employee Referral Program
  • Corporate Sponsored Events & Community Outreach
  • Care.com annual membership
  • Employee Assistance Program
  • Supplemental Benefits via Corestream (Critical Care, Hospital Indemnity, Accident Insurance, Legal Assistance and ID theft protection, etc.)
  • Position may be eligible for a discretionary variable incentive bonus

About Guidehouse
Guidehouse is an Equal Opportunity Employer-Protected Veterans, Individuals with Disabilities or any other basis protected by law, ordinance, or regulation.
Guidehouse will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable law or ordinance including the Fair Chance Ordinance of Los Angeles and San Francisco.
If you have visited our website for information about employment opportunities, or to apply for a position, and you require an accommodation, please contact Guidehouse Recruiting at 1-571-633-1711 or via email at RecruitingAccommodation@guidehouse.com. All information you provide will be kept confidential and will be used only to the extent required to provide needed reasonable accommodation.
All communication regarding recruitment for a Guidehouse position will be sent from Guidehouse email domains including @guidehouse.com or guidehouse@myworkday.com. Correspondence received by an applicant from any other domain should be considered unauthorized and will not be honored by Guidehouse. Note that Guidehouse will never charge a fee or require a money transfer at any stage of the recruitment process and does not collect fees from educational institutions for participation in a recruitment event. Never provide your banking information to a third party purporting to need that information to proceed in the hiring process.
If any person or organization demands money related to a job opportunity with Guidehouse, please report the matter to Guidehouse's Ethics Hotline. If you want to check the validity of correspondence you have received, please contact recruiting@guidehouse.com. Guidehouse is not responsible for losses incurred (monetary or otherwise) from an applicant's dealings with unauthorized third parties.
Guidehouse does not accept unsolicited resumes through or from search firms or staffing agencies. All unsolicited resumes will be considered the property of Guidehouse and Guidehouse will not be obligated to pay a placement fee.

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