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Remote Clinical Logistics Jobs (NOW HIRING)

Fortrea

Remote within the US. Job Overview: The Clinical Trial Manager I has ownership in the clinical ... Ensure clinical and ancillary supplies -including import/export logistics and supply destruction ...

Fortrea

Clinical Trial Manager I- Oncology, FSP

Remote within the US. Job Overview: The Clinical Trial Manager I has ownership in the clinical ... Ensure clinical and ancillary supplies -including import/export logistics and supply destruction ...

Fortrea

Remote US or Canadian based. We are seeking candidates with either CAR T or Ophthalmology ... Ensure clinical and ancillary supplies -including import/export logistics and supply destruction ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

Prepare study materials, maintain equipment, and coordinate study logistics to support efficient ... This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA ...

Karius

Clinical Trial Associate

Redwood City, CA · On-site +1

$60K - $91K/yr

Remote (Bay Area preferred) Primary Responsibilities: * Assist study teams with the collection ... Support investigator meeting planning, coordination, and logistics, including preparation of ...

Karius

Clinical Trial Associate

Redwood City, CA · On-site +1

$41 - $56/hr

Remote (Bay Area preferred) Primary Responsibilities: * Assist study teams with the collection ... Support investigator meeting planning, coordination, and logistics, including preparation of ...

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How much do remote clinical logistics jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for remote clinical logistics 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 is a remote clinical logistics professional?

A Remote Clinical Logistics job involves coordinating and managing the supply chain, transportation, and delivery of materials for clinical trials from a remote location. Professionals in this role ensure that investigational drugs, lab samples, and clinical supplies are delivered efficiently and on time to trial sites. They also oversee compliance with regulatory requirements and collaborate with vendors, sponsors, and site staff. Remote positions leverage technology to monitor logistics processes, resolve issues, and maintain communication across geographically dispersed teams.

What are the key skills and qualifications needed to thrive as a remote clinical logistics professional?

To excel in Remote Clinical Logistics, you need strong organizational skills, knowledge of clinical trial processes, and usually a background in healthcare or life sciences. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and logistics software is typically required. Excellent communication, problem-solving ability, and attention to detail are crucial soft skills for coordinating teams and managing timelines remotely. These competencies ensure smooth clinical trial operations, regulatory compliance, and successful collaboration across dispersed teams.

How does a remote clinical logistics professional typically collaborate with cross-functional teams to ensure smooth trial operations?

Remote Clinical Logistics professionals play a vital role in coordinating between clinical research teams, supply chain specialists, and external vendors to ensure that clinical trial materials are delivered on time and in compliance with regulatory standards. They often rely on virtual communication tools and project management software to track shipments, resolve logistical issues, and update stakeholders about potential delays. Regular virtual meetings and clear documentation are essential to keep everyone aligned and maintain the integrity of the trial process. This collaborative environment provides ample opportunities to develop communication and organizational skills while working with diverse teams across regions.

What is the difference between Remote Clinical Logistics vs Remote Clinical Trial Coordinator?

AspectRemote Clinical LogisticsRemote Clinical Trial Coordinator
Required CredentialsTypically requires a background in logistics, supply chain, or healthcare; certifications like CSCP or CLTD are commonRequires knowledge of clinical trial processes; certifications like CCRP or CCRA are beneficial
Work EnvironmentFocuses on managing supply chains, inventory, and distribution for clinical trials remotelyCoordinates trial activities, manages documentation, and communicates with sites remotely
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and healthcare organizationsCommonly employed by clinical research organizations and pharmaceutical firms

Remote Clinical Logistics involves managing the supply chain and logistics for clinical trials remotely, while Remote Clinical Trial Coordinators focus on coordinating trial activities and site communication. Both roles support clinical research but differ in their core responsibilities and required expertise.

More about Remote Clinical Logistics jobs

What cities are hiring for Remote Clinical Logistics jobs?

Cities with the most Remote Clinical Logistics job openings:

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

The most popular types of Clinical Logistics jobs are:

What states have the most Remote Clinical Logistics jobs?

States with the most job openings for Remote Clinical Logistics jobs include:

What job categories do people searching Remote Clinical Logistics jobs look for?

The top searched job categories for Remote Clinical Logistics jobs are:

Remote Clinical Logistics jobs near you
Infographic showing various Remote Clinical Logistics job openings in the United States as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 100% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Study Operations Manager

Beacon Biosignals

Boston, MA • On-site, Remote

$90K - $110K/yr

Full-time, Contractor

PTO

Re-posted 5 days ago

Job description

Beacon Biosignals is transforming precision medicine for the brain, from clinical development to clinical care. For Life Sciences partners, we offer the leading at-home EEG platform for clinical development of novel therapeutics for neurological, psychiatric, and sleep disorders. Our Diagnostics business is building the most comprehensive at-home platform for precision diagnostics, combining EEG and cardiopulmonary signals to deliver reimbursable assessments for sleep and central nervous system disorders. Together, we're changing the way patients are diagnosed and treated for any disorder that affects brain physiology.
As a Clinical Study Operations Manager within the Clinical Study Operations team, you will be responsible for ensuring the successful operational delivery of Beacon's clinical studies, from startup through close-out. You will work closely with sponsors, project teams, and clinical sites to drive efficient study execution and uphold Beacon's commitment to quality, compliance, and scientific rigor.
You will oversee study startup planning, site onboarding and training, and ongoing operational oversight to ensure studies are executed on time and to the highest standards. Acting as a key operational partner to both sponsors and internal teams, you will proactively identify risks, streamline communication, and maintain alignment across stakeholders. In addition, you will foster a culture of quality within the organization by coaching peers on GCP compliance, documentation discipline, version control, and complaint management, strengthening the team's collective operational excellence.
This is a contract-to-hire individual contributor role, fully remote anywhere in the U.S., and will require up to 10% travel. Beacon's robust asynchronous work practices ensure a first-class remote work experience, but we also have in-person office hubs available located in Boston, New York and Paris.
What success looks like:
  • Collaborate with project teams to implement study startup activities, including communication planning, logistics, development of study documentation, and data configuration.
  • Instill confidence with clients on study operations through start up, maintenance and close out activities.
  • Act as the primary point of contact for clinical sites, ensuring smooth operations and clear communication.
  • Provide training to research sites on the use of Beacon's devices and study protocols, ensuring proper device usage and data collection.
  • Monitor project progress, ensuring adherence to timelines, protocols, and quality standards.
  • Maintain compliance with Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and regulatory standards.
  • Foster a culture of quality within the ClinOps and Scientific teams by coaching peers on GCP requirements, documentation discipline, versioning, and complaint management.
  • Address operational issues promptly, escalating through tools like Zendesk and Asana for resolution.
  • Provide actionable feedback from research sites to inform improvements in devices and workflows.

What you will bring:
  • 5+ years of experience in clinical project management or clinical operations roles.
  • Strong organizational and project management skills, with the ability to manage multiple responsibilities effectively.
  • Excellent written and verbal communication skills in English; additional languages are a bonus.
  • A proactive mindset with the ability to identify priorities and anticipate challenges.
  • Meticulous attention to detail, ensuring accuracy in data collection and reporting.
  • Ability to work in a fast paced environment with multiple priorities.
  • Familiarity with GCP, ICH guidelines, and clinical research regulatory requirements.
  • Knowledge of decentralized data collection, compliance and oversight while showing empathy for both patients and sites.
  • A desire to learn more about analytics, statistics, machine learning, and clinical trials.

The salary range for this role is $90,000 - $110,000. Salary ranges are determined using current market compensation data for this role and adjusted based on experience, skills, and location. The base salary is one component of the total compensation package, which includes equity, PTO and other benefits.
At Beacon, we've found that cultural and scientific impact is driven most by those that lead by example. As such, we're always seeking new contributors whose work demonstrates an avid curiosity, a bias towards simplicity, an eye for composability, a self-service mindset, and - most of all - a deep empathy towards colleagues, stakeholders, users, and patients. We believe a diverse team builds more robust systems and achieves higher impact.

Apply