1

Temporary Clinical Trial Operations Jobs in Reston, VA

... clinical trial conduct. * Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations. Your Profile: * Advanced degree in a relevant ...

Senior Medical Officer

Rockville, MD · On-site

$85K - $141K/yr

Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust What You Will Do: We are looking for a Senior Medical Officer to support the National Institute of ...

Senior Medical Officer

Rockville, MD · On-site

$85K - $141K/yr

Clinical Trial Operations Travel Required: None Clearance Required: Ability to Obtain Public Trust What You Will Do: We are looking for a Senior Medical Officer to support the National Institute of ...

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Identify operational, regulatory, financial, and programmatic risks * Assesses and supports meetings, clinical trial assessments and site visits * Monitor and coordinate activities associated with ...

Clinical Research Coordinator

Bethesda, MD

$26 - $34.50/hr

Identify operational, regulatory, financial, and programmatic risks * Assesses and supports meetings, clinical trial assessments and site visits * Monitor and coordinate activities associated with ...

Clinical Research Coordinator

Bethesda, MD · On-site

$26 - $34.50/hr

Identify operational, regulatory, financial, and programmatic risks * Assesses and supports meetings, clinical trial assessments and site visits * Monitor and coordinate activities associated with ...

Showing results 21-40

Temporary Clinical Trial Operations information

See Reston, VA salary details

$18

$41

$73

How much do temporary clinical trial operations jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for temporary clinical trial operations in Reston, VA is $41.60, according to ZipRecruiter salary data. Most workers in this role earn between $33.51 and $45.77 per hour, depending on experience, location, and employer.

What is the difference between Temporary Clinical Trial Operations vs Clinical Trial Coordinators?

AspectTemporary Clinical Trial OperationsClinical Trial Coordinators
CredentialsRelevant experience, sometimes certifications in clinical researchOften require a degree in health sciences or related field, plus certification
Work EnvironmentContract-based, project-specific settings within research organizationsTypically office-based, coordinating daily trial activities
Employer & Industry UsageUsed by CROs, pharmaceutical companies for short-term needsCommonly employed by research sites and hospitals

Temporary Clinical Trial Operations roles focus on short-term, project-specific tasks within clinical research, often requiring specialized experience or certifications. Clinical Trial Coordinators handle ongoing trial management and participant coordination, usually with a background in health sciences. Both roles are essential in the clinical research process but differ mainly in duration, scope, and employment setting.

What are popular job titles related to Temporary Clinical Trial Operations jobs in Reston, VA? For Temporary Clinical Trial Operations jobs in Reston, VA, the most frequently searched job titles are:
What job categories do people searching Temporary Clinical Trial Operations jobs in Reston, VA look for? The top searched job categories for Temporary Clinical Trial Operations jobs in Reston, VA are:
What cities near Reston, VA are hiring for Temporary Clinical Trial Operations jobs? Cities near Reston, VA with the most Temporary Clinical Trial Operations job openings:

Senior Medical Officer- Clinical Oversight & Pediatric Research

Guidehouse

Rockville, MD • On-site

$85K - $141K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 6 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 looking for a Senior Medical Officer to support NIAID/DMID by providing expert guidance on clinical trial oversight, Institutional Review Board (IRB) processes, pediatric clinical care considerations, and clinical safety management. This is a full-time position located in Rockville, MD.
  • Provide advice and recommendations regarding Institutional Review Board (IRB) processes, pediatric clinical care, hospital pharmacy operations, and related healthcare communities.
  • Provide expert guidance on the oversight of clinical trials.
  • Review clinical trial protocols.
  • Review and comment on safety and operational issues associated with DMID-sponsored protocols.
  • Assess serious adverse events arising from clinical trials.
  • Review and provide recommendations regarding the design and safety of clinical trials.
  • Represent DMID in communications with FDA representatives, sponsors, and academic collaborators regarding clinical trial design and implementation.
  • Review safety reports and serve as a safety expert on committees.
  • Participate in standing department meetings, training, and educational activities.
  • Draft policies and guidelines affecting participants enrolled in DMID-sponsored studies.

What You Will Need:
  • Medical degree from an accredited university.
  • Minimum of SIX (6) years of medical, pediatric, clinical research, or clinical trial oversight experience.
  • Experience supporting IRB review processes and clinical study oversight.
  • Experience reviewing clinical trial protocols and safety reports.
  • Knowledge of clinical trial safety monitoring and regulatory compliance.
  • Proficiency with Microsoft Office applications.
  • Superior medical writing skills.
  • 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:
  • Experience supporting pediatric clinical research programs.
  • Familiarity with hospital pharmacy operations and medication safety programs.
  • Experience drafting medical policies, procedures, and regulatory guidance.
  • Experience participating on safety review committees.
  • Knowledge of FDA regulations and Good Clinical Practice (GCP).

The annual salary range for this position is $85,000.00-$141,000.00. 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.

What Guidehouse employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom