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Remote Covance Clinical Research Jobs (NOW HIRING)

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 ...

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 ...

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 25, 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:

Infographic showing various Remote Covance Clinical Research job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Informatician

Remote

Other

Posted 22 days ago


Job description

Clinical Research Informatician

Location: Remote

Duration: Direct Hire FTE

Must Have's:

  • Bachelor’s Degree in Health Information Management or Health Informatics OR B.S. in a clinical field (nursing, etc.) with certification in Health Informatics OR B.S. in informatics, computer science, statistics, biomedical engineering, artificial intelligence with certification in Health Informatics. (Required)
  • Master’s Degree (Preferred)

Minimum 2 years' experience in:

  • Clinical Research
  • Clinical Informatics
  • Information Technology and/or Academic Healthcare Settings

Experience with:

  • Clinical operations, Health Information Management, or Care Management
  • Clinical standards, coding, definitions, ontologies, dictionaries, and taxonomies
  • Clinical Key Performance Indicators (KPIs)
  • Implementing new technologies in clinical settings
  • Healthcare data curation and documentation in a data warehouse

Proficiency in:

  • SQL and Python or similar coding languages
  • Liaising between clinical stakeholders and technical teams

Expertise in:

  • Analyzing and optimizing clinical workflows to improve efficiency and patient outcomes

Summary:

The Clinical Research Informatician is a bridge between clinicians/researchers and data. They blend their knowledge of clinical workflow, terminology, and practices with an understanding of health information technology to advance clinical and translational research towards improved patient care. The Clinical Informatician will play an integral role focused on creating, testing, implementing, and maintaining applications and data for clinical areas. Responsibilities include acting as a liaison between clinicians/researchers and data stewards, interfacing with stakeholders on informatics software development, maintenance, and operations, and creating streamlined workflows for the exploitation of healthcare data.