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Overnight Duke Clinical Research Jobs (NOW HIRING)

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

At Duke, we celebrate individuality and the unique perspectives each team member brings to advancing medicine and improving lives. As a Clinical Research Coordinator within the Department of ...

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh ... As the Clinical Research Coordinator, you will conduct clinical research studies, with a focus on ...

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh ... As the Clinical Research Coordinator, you will conduct clinical research studies, with a focus on ...

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Overnight Duke Clinical Research information

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How much do overnight duke clinical research jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for overnight duke clinical research in the United States is $30.16, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $31.97 per hour, depending on experience, location, and employer.

What is an overnight Duke Clinical Research?

An Overnight Duke Clinical Research position typically involves conducting or supporting clinical trials and research studies at Duke University during overnight hours. This role may include monitoring patients, collecting data, ensuring compliance with study protocols, and working closely with clinical staff and researchers. The overnight schedule is crucial for studies that require 24-hour monitoring or data collection. Candidates for this role should be comfortable working night shifts and have strong organizational and communication skills. This position plays a vital part in advancing medical knowledge and patient care through research.

What skills and qualifications are needed to thrive as an overnight Duke Clinical Research?

To thrive as an Overnight Duke Clinical Research professional, you need a solid background in clinical research practices, strong attention to detail, and typically a bachelor's degree in a health or science-related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and compliance with regulations such as GCP is essential. Exceptional organizational skills, problem-solving abilities, and effective communication are key soft skills for managing complex studies and collaborating with diverse teams. These competencies are crucial to ensure the integrity of data collection, adherence to protocols, and the overall success of clinical research conducted during overnight shifts.

What unique challenges do overnight Duke Clinical Research staff face, and how can they be addressed?

Working overnight shifts in Duke Clinical Research often involves managing studies that require 24/7 subject monitoring or time-sensitive interventions. Staff may face challenges such as maintaining alertness during late hours, coordinating with daytime teams for seamless communication, and handling urgent participant needs with limited on-site resources. To address these challenges, it’s important to establish clear handoff protocols, utilize technology for real-time updates, and practice good sleep hygiene and self-care outside of work. Teamwork and open communication play a crucial role in ensuring the success and safety of overnight research operations.

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

AspectOvernight Duke Clinical ResearchClinical Research Coordinator
CertificationsOften requires GCP training, CPR, and sometimes clinical research certificationsTypically requires GCP training, CPR, and research certifications
Work EnvironmentHospital or clinical research facility, overnight shifts possibleResearch sites, hospitals, or clinics, usually daytime hours
Employer & IndustryAcademic medical centers, research institutions, pharmaceutical companiesHospitals, research organizations, academic institutions

Overnight Duke Clinical Research roles focus on conducting clinical trials during overnight hours, often requiring specific certifications and working in hospital or research settings. Clinical Research Coordinators typically work daytime hours managing patient visits and data collection. Both roles are essential in clinical research but differ mainly in shift timing and daily responsibilities.

What cities are hiring for Overnight Duke Clinical Research jobs?

Cities with the most Overnight Duke Clinical Research job openings:

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

The most popular types of Duke Clinical Research jobs are:

What states have the most Overnight Duke Clinical Research jobs?

States with the most job openings for Overnight Duke Clinical Research jobs include:

Clinical Research Coordinator

Duke University

Durham, NC

$23.50 - $31.25/hr

Full-time

Medical, Dental, Retirement

Re-posted 9 days ago


Duke University rating

6.7

Company rating: 6.7 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

488th of 620 rated colleges and universities


Job description

School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations.

Be You. Be Bold. Choose Duke.

Clinical Research Coordinator - Neurosurgery Research


Be You.

At Duke, we celebrate individuality and the unique perspectives each team member brings to advancing medicine and improving lives. As a Clinical Research Coordinator  within the Department of Neurosurgery, you will join a highly collaborative team dedicated to groundbreaking clinical research in both adult and pediatric populations. Our studies span Parkinson's disease, Alzheimer's disease, epilepsy, neuro-oncology, rare genetic disorders, traumatic brain and spinal injuries, chronic pain, and other complex neurological conditions.

You'll work alongside nationally recognized neurosurgeons, neuro-oncologists, scientist-clinicians, and PhD researchers who are passionate about discovery, innovation, and transforming patient care. If you thrive in a dynamic academic research environment and enjoy solving complex challenges while making a meaningful impact, Duke Neurosurgery offers an exceptional opportunity to grow your career.


Be Bold.

What You'll Do

As a senior clinical research professional, you will lead and support complex clinical trials throughout the study lifecycle while serving as a trusted resource for research teams, sponsors, and investigators.

Clinical Trial Operations

  • Coordinate and manage complex clinical research studies, including drug, device, and procedural trials involving randomization, blinding, crossover designs, and investigational products.
  • Maintain study documentation and regulatory records to ensure continuous compliance with institutional, sponsor, FDA, and international requirements.
  • Prepare and support FDA submissions in partnership with regulatory experts and investigators.
  • Manage investigational products, including receipt, storage, accountability, tracking, and participant dispensing.
  • Serve as a primary liaison with sponsors, Contract Research Organizations (CROs), Investigational Drug Services (IDS), and internal stakeholders.
  • Lead study monitoring, audit preparation, and corrective action activities.
  • Support study startup, feasibility assessments, ongoing project management, and study closeout activities.

Participant Recruitment & Retention

  • Develop and implement recruitment and retention strategies for complex clinical research studies.
  • Screen, enroll, and monitor research participants while ensuring protocol adherence and participant safety.
  • Identify barriers to enrollment and retention and implement solutions that enhance study performance.
  • Conduct study visits in accordance with approved protocols and regulatory requirements.
  • Participate in an established on-call research coverage rotation supporting critical care research activities.

Regulatory & Ethical Compliance

  • Lead IRB submissions, amendments, continuing reviews, and safety reporting activities.
  • Conduct informed consent discussions for studies involving greater-than-minimal risk and complex interventions.
  • Collaborate with investigators to assess adverse events, determine reportability requirements, and maintain participant safety oversight.
  • Develop and maintain regulatory tools, templates, standard operating procedures, and compliance resources.

Data & Research Excellence

  • Ensure the integrity, quality, security, and completeness of research data.
  • Utilize clinical research systems and electronic data capture tools to support protocol execution and reporting.
  • Apply FAIR data principles and open science practices to facilitate data sharing and reproducibility.
  • Support data management activities, including data cleaning, validation, quality assurance, database testing, and reporting.
  • Create study progress reports, visualizations, summaries, and presentations for investigators and stakeholders.
  • Assist with qualitative and quantitative data analyses using software such as SAS, R, SPSS, NVivo, or Atlas.ti.

Scientific Contribution

  • Participate in protocol development, scientific literature reviews, and grant proposal preparation.
  • Contribute to abstracts, presentations, posters, and peer-reviewed publications.
  • Serve as an author or co-author on research dissemination activities when appropriate.

Leadership & Collaboration

  • Mentor, train, and support research staff and study teams.
  • Lead or contribute to multidisciplinary meetings involving investigators, sponsors, research partners, and institutional stakeholders.
  • Share best practices and help develop operational resources that improve research performance.
  • Serve on committees, workgroups, and professional development initiatives that advance Duke's research mission.
  • Continuously expand expertise through professional development, certifications, and participation in research-focused educational opportunities.

What You'll Bring

Required Qualifications

  • Bachelor's degree in a health-related, scientific, or research discipline, or an equivalent combination of education and experience.
  • Experience coordinating clinical research studies with progressive responsibility.
  • Demonstrated knowledge of clinical research regulations, Good Clinical Practice (GCP), FDA requirements, and human subject protections.
  • Experience managing multiple priorities in a fast-paced research environment.
  • Strong organizational, communication, problem-solving, and project management skills.

Preferred Qualifications

  • Experience supporting neurology, neurosurgery, neuro-oncology, critical care, or device-based clinical research.
  • Experience with investigational product management and complex interventional clinical trials.
  • Knowledge of OnCore, eReg, Maestro Care/Epic, REDCap, or other clinical research systems.
  • Professional certification such as CCRP, CCRC, ACRP, or SOCRA certification.
  • Experience contributing to publications, grant submissions, or scientific presentations.

Key Competencies

  • Clinical trial management
  • Regulatory compliance
  • Participant engagement and retention
  • Data quality and data management
  • Cross-functional collaboration
  • Critical thinking and problem solving
  • Scientific communication
  • Leadership and mentorship
  • Adaptability and resilience
  • Continuous improvement mindset

Choose Duke.

At Duke, you'll find more than a job. You'll find a community committed to innovation, excellence, and improving human health.

Why Duke?

  • Work alongside world-renowned clinicians, researchers, and educators.
  • Contribute to pioneering neuroscience and neurosurgical discoveries.
  • Join a collaborative team culture built on respect, inclusion, and shared success.
  • Access extensive professional development, training, and career advancement opportunities.
  • Support research that directly impacts patients and families around the world.

A Culture of Belonging

Duke is committed to fostering an environment where every individual feels valued, respected, and empowered to contribute. We believe diverse backgrounds, experiences, and perspectives fuel innovation and strengthen our ability to improve lives through research, education, and patient care.


Ready to Make a Difference?

Apply now and help advance life-changing neuroscience research while building a meaningful career with Duke University School of Medicine.


Anticipated Pay Range: Duke University provides an annual base salary range for this position as USD $61,026.00 to USD $101,959.00. Duke University considers factors such as (but not limited to) scope and responsibilities of the position; candidate's work experience, education/training, and key skills; internal peer equity; as well as market and organizational considerations when extending an offer.


Your total compensation goesbeyond the dollars on your paycheck. Duke provides comprehensive and competitive medical and dental care programs, generous retirement benefits, and a wide array of family-friendly and cultural programs to eligible team members. Learn more at: https://hr.duke.edu/benefits/


Equal Opportunity Employer: Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender,gender expression, gender identity, genetic information, national origin, race, religion, sex (including pregnancy and pregnancy- related conditions), sexual orientation, or military status.


Duke aspires to create a community built oncollaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas-an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values.


Essential Physical Job Functions:
Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and reasonable accommodation(s) can be requested with Duke Access and Accommodations Services (email: DAAS@duke.edu; phone: 919-668-1267).

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About Duke University

Sourced by ZipRecruiter

Duke is regarded as one of America's leading research universities. Located in Durham, North Carolina, Duke is positioned in the heart of the Research Triangle, which is ranked annually as one of the best places in the country to work and live. Duke has more than 15,000 students who study and conduct research in its 10 undergraduate, graduate, and professional schools. With about 40,000 employees, Duke is the third largest private employer in North Carolina, and it now has international programs in more than 150 countries.

Industry

Colleges, universities, and professional schools and hospitals

Company size

10,000+ Employees

Headquarters location

Durham, NC, US