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Remote Covance Clinical Research Jobs (NOW HIRING)

Trice Healthcare

Clinical Research Informatician

Remote Duration: Direct Hire FTE Must Have's: * Bachelor's Degree in Health Information Management ... Clinical Research * Clinical Informatics * Information Technology and/or Academic Healthcare ...

WEP Clinical

Senior Clinical Research Associate

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 ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

This position is not eligible for employment sponsorship. #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a leading global provider of clinical research services, commercial insights and healthcare ...

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Remote Covance Clinical Research information

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$49K

$107.3K

$189K

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

As of Aug 7, 2026, the average yearly pay for remote covance clinical research 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 a remote Covance clinical research associate?

A Remote Covance Clinical Research job involves working for Covance, a leading contract research organization (CRO), to support clinical trials and research projects from a remote location. These roles typically include positions like clinical research associate, project manager, or data manager, where you monitor clinical trials, collect and analyze data, and ensure compliance with regulatory guidelines. Working remotely allows employees to contribute to important medical research while enjoying flexibility in their work environment. Covance provides training, support, and access to digital tools required for remote collaboration. These positions are vital in bringing new treatments and drugs to market efficiently and safely.

What are some common challenges faced by remote clinical research associates at Covance, and how can they be managed effectively?

Remote Clinical Research Associates (CRAs) at Covance often encounter challenges such as maintaining effective communication with on-site teams, managing time zones, and ensuring data accuracy without direct site visits. To address these issues, CRAs use advanced digital tools for virtual monitoring, schedule regular check-ins with site staff, and participate in collaborative platforms to stay updated. Proactive communication and strong organizational skills are essential for success in this remote environment, helping to maintain high-quality standards and meet project deadlines.

What are the key skills and qualifications needed to thrive as a remote clinical research associate at Covance, and why are they important?

To thrive as a Remote Clinical Research Associate at Covance, you typically need a background in life sciences, experience in clinical trials, and a relevant degree such as a BSc in a scientific field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational skills, attention to detail, and effective communication are essential soft skills for managing remote study sites and collaborating with cross-functional teams. These competencies ensure protocol compliance, high-quality data collection, and smooth trial operations in a remote environment.

What is the difference between Remote Covance Clinical Research vs Remote Clinical Research Associate?

AspectRemote Covance Clinical ResearchRemote Clinical Research Associate
CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCR or RAC are commonRequires a degree in life sciences or related field; certifications like CCR are often preferred
Work EnvironmentConducted remotely, often within a CRO setting, supporting multiple clinical trialsPrimarily remote, overseeing clinical trial sites, ensuring protocol compliance
Employer & Industry UsageUsed by CROs like Covance, in pharmaceutical and biotech industriesCommonly employed by CROs, pharmaceutical companies, and biotech firms

Remote Covance Clinical Research roles focus on supporting clinical trials within Covance's CRO environment, often involving data management and trial coordination. Remote Clinical Research Associates primarily oversee trial sites, monitor progress, and ensure compliance. Both roles require similar credentials and are often remote, but their specific responsibilities differ within the clinical research process.

More about Remote Covance Clinical Research jobs
What cities are hiring for Remote Covance Clinical Research jobs? Cities with the most Remote Covance Clinical Research job openings:
What are the most commonly searched types of Covance Clinical Research jobs? The most popular types of Covance Clinical Research jobs are:
What states have the most Remote Covance Clinical Research jobs? States with the most job openings for Remote Covance Clinical Research jobs include:
What job categories do people searching Remote Covance Clinical Research jobs look for? The top searched job categories for Remote Covance Clinical Research jobs are:
Remote Covance Clinical Research jobs near you
Infographic showing various Remote Covance Clinical Research job openings in the United States as of August 2026, with employment types broken down into 59% Full Time, 25% Part Time, 8% Temporary, and 8% Contract. Highlights an 100% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Assistant

Allen Spolden

Silver Spring, MD • Remote

$45K - $55K/hr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 15 days ago

Job description

This is a remote position.

Position Overview

We are seeking a motivated and detail-oriented Clinical Research Assistant to join our growing clinical operations team. In this role, you will support the coordination and administration of clinical research studies while ensuring study documentation, data quality, and regulatory compliance are maintained throughout the research process.

This position is ideal for someone with excellent organizational skills, strong attention to detail, and an interest in contributing to clinical research in a remote environment.

Essential Responsibilities
  • Assist with the day-to-day management of assigned clinical studies.
  • Maintain investigator site files, regulatory binders, and essential study documents.
  • Prepare, review, and file research documentation in accordance with study requirements.
  • Support participant scheduling and study visit coordination.
  • Enter, verify, and reconcile clinical data within electronic research systems.
  • Monitor study timelines and assist with tracking project deliverables.
  • Communicate effectively with investigators, sponsors, study participants, and internal research teams.
  • Identify and escalate documentation discrepancies or protocol deviations when appropriate.
  • Ensure research activities are conducted in compliance with ICH Good Clinical Practice (GCP), study protocols, and applicable regulatory requirements.
  • Perform additional administrative and research support duties as assigned.


RequirementsQualifications
Required
  • Bachelor's degree in Life Sciences, Health Sciences, Nursing, Public Health, or a related discipline, or equivalent healthcare experience.
  • Strong organizational and problem-solving abilities.
  • Excellent verbal and written communication skills.
  • High level of accuracy and attention to detail.
  • Proficiency with Microsoft Office and web-based software applications.
  • Ability to manage multiple priorities while working independently in a remote setting.
Preferred
  • Previous experience supporting clinical research or healthcare operations.
  • Familiarity with ICH-GCP guidelines and FDA regulations.
  • Experience using Electronic Data Capture (EDC), CTMS, or eTMF systems.
  • Knowledge of clinical trial documentation and research workflows.
Work Schedule
  • Full-time
  • Monday through Friday
  • Standard business hours


BenefitsBenefits
  • Competitive salary
  • Comprehensive medical, dental, and vision coverage
  • 401(k) with employer contribution
  • Paid time off and company holidays
  • Remote work environment
  • Professional development and career advancement opportunities