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Overnight Clinical Trials Jobs (NOW HIRING)

CenExel

Clinical Research Coordinator I

Gaithersburg, MD · On-site

$26.90 - $34.35/hr

Job Summary: Responsible for assisting with coordinating clinical trials with the strictest ... Overnight travel may be required for training and/or investigative meetings. CenExel Clinical ...

CenExel

Clinical Research Coordinator II

Marlton, NJ · On-site

$26.24 - $33.51/hr

Job Summary: Responsible for coordinating all aspects of clinical trials with the strictest ... Overnight travel may be required for training and/or investigative meetings. CenExel Clinical ...

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Overnight Clinical Trials information

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How much do overnight clinical trials jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for overnight clinical trials in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What are overnight clinical trials?

Overnight clinical trials are research studies where participants are required to stay at a clinical facility for one or more nights. These trials are conducted to monitor the effects of experimental medications or treatments under controlled conditions, especially during sleep or over extended periods. Participants are closely observed by medical staff to ensure safety and collect accurate data. Such trials are essential for testing the safety, side effects, and efficacy of new drugs before they are approved for general use.

What are the key skills and qualifications needed to thrive as an overnight clinical trials coordinator?

To thrive as an Overnight Clinical Trials Coordinator, you need a solid understanding of clinical research protocols, data collection, and patient safety, typically supported by a degree in life sciences or nursing. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC), and adherence to Good Clinical Practice (GCP) guidelines is essential. Strong attention to detail, problem-solving skills, and the ability to communicate effectively during night shifts make candidates stand out. These skills are critical for ensuring accuracy, regulatory compliance, and participant well-being during clinical studies conducted outside standard hours.

What are some unique challenges faced by professionals working overnight shifts in clinical trials?

Working overnight in clinical trials often means adapting to irregular sleep patterns and managing fatigue, which can be challenging for some individuals. Overnight staff are responsible for monitoring participants, collecting data, and responding to any medical concerns that arise during non-traditional hours, requiring strong attention to detail and adaptability. Team communication is crucial, as overnight professionals must coordinate effectively with day-shift colleagues to ensure seamless participant care and accurate data handover. Despite the challenges, overnight roles can offer opportunities to develop specialized skills, take on additional responsibilities, and advance within clinical research operations.

What is the difference between Overnight Clinical Trials vs Clinical Research Coordinators?

AspectOvernight Clinical TrialsClinical Research Coordinators
CredentialsTypically require clinical trial experience, sometimes certifications like CCRPRequire degrees in health or related fields, often certifications like CCRP or CCRC
Work EnvironmentConducts trials during overnight hours, often in clinical settings or labsWork during regular business hours in hospitals, clinics, or research centers
Employer & IndustryPharmaceutical companies, research institutions, CROsHospitals, research institutions, pharmaceutical companies
Search & Comparison IntentFocuses on night shift clinical trial rolesFocuses on coordinating clinical research activities

Overnight Clinical Trials involve conducting clinical research during nighttime hours, often requiring specialized experience and night shift availability. Clinical Research Coordinators typically work during daytime hours managing and coordinating clinical studies. While both roles are essential in clinical research, they differ mainly in work hours and specific responsibilities.

What cities are hiring for Overnight Clinical Trials jobs?

Cities with the most Overnight Clinical Trials job openings:

What are the most commonly searched types of Clinical Trials jobs?

The most popular types of Clinical Trials jobs are:

What states have the most Overnight Clinical Trials jobs?

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

Overnight Clinical Trials jobs near you

Global Director, Clinical Project Management

SystImmune, Inc

Princeton, NJ • On-site

$180K - $230K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 12 days ago

Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
We are seeking a highly skilled and motivated Global Director, Clinical Project Management (CPM) to join our dynamic team. The successful candidate will oversee and coordinate global clinical trials from initiation through to completion. This role involves ensuring compliance with regulatory requirements, managing study timelines and budgets, and fostering effective communication among stakeholders. The global Director, Clinical Project Management will play a critical role in delivering high-quality data and ensuring the success of clinical studies.
This position requires onsite hybrid work model in Princeton, NJ.
Responsibilities
  • Oversee the planning and execution of global clinical trials
  • Develop and implement study protocols, timelines, and budgets.
  • Manage all aspects of clinical trial operations, including site selection, initiation, monitoring, and closeout.
  • Ensure compliance with Good Clinical Practice (GCP) and regulatory guidelines.
  • Coordinate with cross-functional teams, including investigators, vendors, and regulatory bodies.
  • Monitor trial progress and manage data collection to ensure accuracy and integrity.
  • Identify and mitigate project risks
  • Oversee a team of regional CPMs, CRAs and CTAs.
  • Ensure the preparation and submission of regulatory documents are compliant with local regulatory standards and maintained per good clinical practice.
  • Conduct regular meetings with study teams and provide updates to stakeholders.
  • Coordinate with external vendors and partners involved in the trial
  • Support development of key process initiatives and SOPs internally
  • Oversee vendors supporting trial execution

Qualifications
  • Bachelor's degree in Life Sciences, Nursing, or a related field.
  • Minimum of 10 years of experience in clinical trial management, including at least 5 years in a direct line management role.
  • Strong understanding of GCP and regulatory requirements.
  • Excellent organizational and project management skills.
  • Proven ability to lead cross-functional teams and manage multiple priorities.
  • Strong communication and interpersonal skills.
  • Ability to work collaboratively in a team-oriented environment
  • Flexibility and adaptability to changing priorities and workload
  • Master's degree in a related field or clinical research certification (e.g., ACRP or SOCRA).
  • Experience with electronic data capture (EDC) systems and clinical trial management software.
  • Prior experience in running or supporting Oncology clinical trials a plus.
  • Previous experience in a sponsor or CRO environment.

Location/Travel:
  • Princeton NJ onsite in office
  • Overnight travel ~25%

Compensation and Benefits:
The expected base salary range for this position is $180,000 - $230,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's qualifications, experience, and skills.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

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