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Remote Clinical Research Startup Jobs (NOW HIRING)

Remote Flexibility: Most study coordination activities can be performed remotely, including patient ... Serve as the primary Clinical Research Coordinator for the study and work closely with the ...

... various clinical research related tasks and requirements. Some understanding of basic medical ... We are a San Francisco based startup, backed by leading venture funds and industry leaders.

Remote Hours: Day 5x8-Hour (08:00 - 17:00) Contract Length: Four months Start Date: 9/8/26 or later ... The team works with investigators, study teams, sponsors, CROs, Contracts, Research Finance ...

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ...

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical ... They conduct on-site and remote monitoring to ensure protocol adherence, maintain essential ...

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Remote Clinical Research Startup information

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$49K

$107.3K

$189K

How much do remote clinical research startup jobs pay per year?

As of Sep 5, 2026, the average yearly pay for remote clinical research startup in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is the difference between Remote Clinical Research Startup vs Remote Clinical Research Coordinator?

AspectRemote Clinical Research StartupRemote Clinical Research Coordinator
CredentialsTypically requires a degree in life sciences or related field; certifications like CCR or RAC are commonRequires a degree in health sciences, nursing, or related; certifications like CCRP are preferred
Work EnvironmentStartups often operate remotely or hybrid, focusing on innovative clinical trial solutionsPrimarily remote, coordinating clinical trial activities across sites and participants
Employer & Industry UsageFound in biotech, pharma startups, and CROs focusing on new trial methodsCommon in hospitals, research institutions, and CROs managing trial logistics

The main difference is that Remote Clinical Research Startups focus on developing new clinical trial technologies and often have a broader, innovative scope, while Remote Clinical Research Coordinators handle the day-to-day management of clinical trials, ensuring protocol adherence and data collection. Both roles require relevant certifications and work in remote or hybrid environments, but their responsibilities and industry focus differ.

More about Remote Clinical Research Startup jobs

What cities are hiring for Remote Clinical Research Startup jobs?

Cities with the most Remote Clinical Research Startup job openings:

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

The most popular types of Clinical Research Startup jobs are:

What states have the most Remote Clinical Research Startup jobs?

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

Infographic showing various Remote Clinical Research Startup job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Remote Locums Cardiology Opportunity - Clinical Trial ECG Review | Flexible Part-Time Schedule | Bos

Aya Locums

Boston, MA • Remote

Other

Posted 8 days ago


Job description

Position Overview

Seeking a Board-Certified Cardiologist for a remote clinical trial support opportunity focused on centralized ECG interpretation and regulatory-compliant review processes. This role offers flexible telehealth scheduling while supporting a Boston-based clinical research program.

Schedule

  • Remote/telehealth opportunity
  • Monday–Friday coverage required
  • Flexible workload averaging 10–20 hours per week
  • No call responsibilities

Clinical Responsibilities

  • Centralized review and interpretation of protocol-specific ECGs for regulated clinical trials
  • Evaluate ECG parameters including:
    • Heart rate
    • PR interval
    • QRS duration
    • QT/QTc measurements
  • Identify abnormalities including:
    • Arrhythmias
    • Conduction abnormalities
    • QT prolongation
    • Ischemic changes
  • Escalate clinically significant findings according to study protocol timelines
  • Ensure consistency and adherence to standardized interpretation methodologies

Preferred Experience

  • Prior centralized ECG review or clinical trials experience preferred
  • Familiarity with clinical trial workflows and electronic ECG systems
  • Understanding of:
    • ALCOA++ principles
    • ICH E6 (GCP)
    • ICH E14 (QT/QTc evaluation)
    • FDA/EMA safety expectations and audit requirements

Requirements

  • Board-Certified Cardiologist required
  • Active medical license in at least one state required
  • Minimum 1 year of experience required

Credentialing

  • Fast credentialing timeline of approximately 2 weeks

Additional Highlights

  • Fully remote opportunity with flexible weekly hours
  • Ideal supplemental assignment for providers seeking non-clinical bedside work
  • Long-term clinical research exposure within a highly regulated environment