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Overnight Clinical Research Jobs in Reston, VA (NOW HIRING)

CenExel

Clinical Research Coordinator I

Gaithersburg, MD · On-site

$26.90 - $34.35/hr

Overnight travel may be required for training and/or investigative meetings. CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without ...

MAPMG

Hospital and EMU Rounder - Nocturnist

Lanham, MD · On-site

$280K/yr

... research. What You Can Expect: * Provide comprehensive overnight medical care, including admissions, cross-coverage, management of acute clinical issues, participation in medical emergencies and code ...

MAPMG

Hospital and EMU Rounder - Nocturnist

Lanham, MD · On-site

$280K/yr

... research. What You Can Expect: * Provide comprehensive overnight medical care, including admissions, cross-coverage, management of acute clinical issues, participation in medical emergencies and code ...

MAPMG

Hospital and EMU Rounder- Nocturnist

Lanham, MD · On-site

$280K/yr

... research. What You Can Expect: * Provide comprehensive overnight medical care, including admissions, cross-coverage, management of acute clinical issues, participation in medical emergencies and code ...

MAPMG

Hospital and EMU Rounder- Nocturnist

Lanham, MD · On-site

$280K/yr

... research. What You Can Expect: * Provide comprehensive overnight medical care, including admissions, cross-coverage, management of acute clinical issues, participation in medical emergencies and code ...

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Overnight Clinical Research information

See Reston, VA salary details

$51K

$111.7K

$196.6K

How much do overnight clinical research jobs pay per year?

As of Aug 25, 2026, the average yearly pay for overnight clinical research in Reston, VA is $111,668.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,300.00 and $127,400.00 per year, depending on experience, location, and employer.

What is an overnight clinical research job?

Overnight clinical research jobs involve working non-traditional hours, typically overnight shifts, to oversee clinical trials or studies that require 24/7 monitoring of participants. Employees in these roles may collect data, monitor patient safety, administer medications, and ensure compliance with study protocols during nighttime hours. These positions are crucial for studies where continuous observation is necessary, such as sleep research or trials involving inpatient monitoring.

What are the key skills and qualifications needed to thrive as an overnight clinical research professional?

To thrive as an Overnight Clinical Research professional, you need a background in life sciences or nursing, experience in clinical trial protocols, and often a relevant degree or certification such as GCP (Good Clinical Practice). Familiarity with data collection software, electronic data capture (EDC) systems, and basic laboratory equipment is typically necessary. Attention to detail, strong organizational skills, and the ability to communicate clearly are valuable soft skills for this role. These competencies ensure accurate data collection, adherence to regulatory standards, and effective teamwork during late or overnight shifts critical to research integrity.

What are the unique challenges of working overnight shifts in clinical research, and how can professionals manage them?

Overnight shifts in clinical research often require adapting to non-traditional hours while maintaining high attention to detail and protocol compliance. Common challenges include managing fatigue, coordinating with day-shift team members, and ensuring effective communication across shift changes. Professionals can manage these by establishing a consistent sleep routine, leveraging handover tools, and participating in regular team meetings. Working overnight can also offer valuable experience with independently handling study procedures and troubleshooting issues, which can be advantageous for career growth.

What is the difference between Overnight Clinical Research vs Clinical Research Coordinator?

AspectOvernight Clinical ResearchClinical Research Coordinator
CredentialsTypically requires a background in healthcare or life sciences, sometimes with certifications like CCRCRequires similar credentials, often with clinical research certifications or degrees in health sciences
Work EnvironmentConducts research activities during overnight hours, often in clinical settings or labsWorks during daytime hours in hospitals, clinics, or research facilities
Employer & Industry UsageFound in clinical trial sites, hospitals, and research institutionsEmployed by research organizations, hospitals, and pharmaceutical companies
Common Search & ComparisonOften compared due to scheduling differences and similar roles in clinical trials

Overnight Clinical Research involves conducting clinical trial activities during overnight shifts, focusing on data collection and patient monitoring. Clinical Research Coordinators typically work during regular hours, managing trial logistics and patient recruitment. Both roles require similar credentials and are integral to clinical trials, but differ mainly in work hours and specific responsibilities.

What are the most commonly searched types of Clinical Research jobs in Reston, VA?

The most popular types of Clinical Research jobs in Reston, VA are:

What cities near Reston, VA are hiring for Overnight Clinical Research jobs?

Cities near Reston, VA with the most Overnight Clinical Research job openings:

Overnight Clinical Research jobs near you

Clinical Research Coordinator I

Gaithersburg, MD

CBH Health LLC.
11 - 50 employees
Learn more about CBH Health LLC.external

$26.90 - $34.35/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 26 days ago

Job description

About Us:

CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and integrated operations optimize every step of the clinical trial process.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation of, and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.

Job Summary:

Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.

Compensation:  $26.90-$34.35 /hr  depending on education, experience and skillset

Essential Responsibilities and Duties:

  • Assists with coordinating all aspects of patient involvement from study initiation until study completion.
  • Organizes research information for clinical trials.
  • Observes subjects and assists with data analysis and reporting.
  • Schedules the collection of data.
  • Documents adverse events, protocol deviations, and other unanticipated problems appropriately.
  • Reports research data to maintain quality and compliance.
  • Performs administrative and regulatory duties related to the study as appropriate.
  • Participates in other protocol development activities.
  • Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
  • Educates potential participants and caregivers on protocol specific details and expectations.
  • Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.

Education/Experience/Skills:

  • High school graduate or equivalent; Bachelors Degree, preferred.
  • 0-3 years of experience in the medical field.
  • Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
  • Strong leadership and mentorship skills.
  • Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
  • Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations.
  • Works independently as well as functioning as part of a team.
  • Must be able to effectively communicate verbally and in writing.

 

Working Conditions

  1. Indoor, Office environment.
  2. Shift work, depending on location.
  3. Essential physical requirements include sitting, typing, standing, and walking.
  4. Lightly active position, occasional lifting of up to 20 pounds. Rarely lift over 20 pounds.
  5. Reporting to work, as scheduled, is essential.
  6. Overnight travel may be required for training and/or investigative meetings.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.

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