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Remote Tribe Clinical Research Jobs (NOW HIRING)

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 ...

Ōura

Clinical Research Coordinator

$24.75 - $33/hr

We are looking for a Clinical Research Coordinator to join our Clinical Research Operations team ... This is a remote US role, with a preference for candidates based in San Francisco, Boston, or San ...

New

IQVIA

Clinical Research Coordinator

Philadelphia, PA · Remote

$35 - $42/hr

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

Danaher

Sr. Clinical Research Associate

The position will be fully remote within the United States. In this role, you will have the ... clinical research experience OR Doctoral degree in field with 0-2 years clinical research ...

Hanger, Inc.

Director of Clinical Research

$140K - $150K/yr

The Director of Clinical Research will serve within Hanger's Department of Clinical and Scientific ... Remote: Pay range of $140,000- $150,000 + bonus + benefits. This pay range is posted to comply with ...

New

Essentia Health

Clinical Research Assistant

Duluth, MN · On-site +1

$18.69 - $27.85/hr

Experience in oncology, clinical research, academic research or similar area. Over 1 year computer ... None FTE: 1 Possible Remote/Hybrid Option: Shift Rotation: Day Rotation (United States of America ...

Danaher

Senior Clinical Research Associate

The Sr. Clinical Research Associate (Sr. CRA) is responsible for set-up, initiation, execution ... The position will be fully remote within the United States. In this role, you will have the ...

Danaher

Senior Clinical Research Associate

The Sr. Clinical Research Associate (Sr. CRA) is responsible for set-up, initiation, execution ... The position will be fully remote within the United States. In this role, you will have the ...

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Remote Tribe Clinical Research information

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$49K

$107.3K

$189K

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

As of Jul 15, 2026, the average yearly pay for remote tribe 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 the difference between Remote Tribe Clinical Research vs Remote Clinical Data Coordinator?

AspectRemote Tribe Clinical ResearchRemote Clinical Data Coordinator
CredentialsTypically requires a degree in health sciences, life sciences, or related field; certifications like CCRP are a plusRequires a degree in health sciences, life sciences, or related field; familiarity with data management systems
Work EnvironmentRemote, often in research organizations or pharmaceutical companiesRemote, primarily in clinical research or healthcare settings
Employer & IndustryResearch organizations, pharmaceutical companies, biotech firmsClinical research sites, pharmaceutical companies, CROs

Remote Tribe Clinical Research and Remote Clinical Data Coordinator roles share similar credentials and work environments, focusing on supporting clinical trials remotely. However, the Clinical Research role often involves broader responsibilities in trial management, while Data Coordinators focus specifically on data entry and management tasks.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate working remotely, and why are they important?

To thrive as a Remote Clinical Research Associate, you need a solid background in life sciences, clinical trial processes, and regulatory compliance, often supported by a relevant degree and experience in clinical research. Familiarity with electronic data capture (EDC) systems, trial management software, and certifications like GCP (Good Clinical Practice) are typically required. Exceptional organizational skills, attention to detail, and effective virtual communication set top candidates apart. These skills ensure accurate trial monitoring, regulatory adherence, and successful collaboration across geographically dispersed teams.

What are some common challenges faced by professionals working in remote clinical research teams, and how can they be addressed?

Professionals in remote clinical research teams often encounter challenges such as maintaining effective communication across different time zones, ensuring data integrity, and fostering team cohesion without in-person interaction. These obstacles can be addressed by utilizing robust project management tools, scheduling regular virtual meetings, and establishing clear protocols for data sharing and documentation. Additionally, fostering a culture of open communication and continuous feedback helps remote team members stay connected and aligned with study objectives.
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Remote Tribe Clinical Research jobs near you
Senior Clinical Research Associate

Senior Clinical Research Associate

Cognitive Research Corporation

Remote

Full-time

Posted 7 days ago

New

Job description

The Senior Clinical Research Associate is responsible for overseeing the execution of clinical trials at Investigative Sites. The Clinical Research Associate acts as a liaison between the study Sponsor, CRC and Investigative Sites. They will proactively identify and resolve clinical project issues and participate in process improvement initiatives as applicable. The CRA facilitates successful execution of studies by Investigative Sites and helps to ensure the rights, safety and welfare of human research participants as well as data integrity in clinical trials.
Essential Duties & Responsibilities
  • Initiates, monitors, and closes-out investigative sites in accordance with FDA/ICH regulations.
  • Tracks and maintains study specific non-Case Report Form database
  • Administers Clinical research projects; collects investigator documentation, site management, clinical contact, and prepare reports as required
  • Ensures appropriate source document review and source document verification as required
  • Reviews Case Report Forms to identify erroneous, missing, or incomplete data
  • Generates queries to resolve problematic data to appropriate personnel, and review responses to assure the database is updated accordingly
  • Verifies study drug accountability; generates and tracks drug shipments and storage
  • Travels as necessary, based on project needs and according to Clinical Monitoring Plan requirements
  • Performs data collection, retrieval, entry and clean up as necessary
  • Develops and maintains strong relationships with Investigator(s) and site staff
  • Independently manages sites resulting in acceptable Quality Assurance reports.
  • Escalates study/site issues/deviations appropriately
  • Serves as lead monitor for a protocol or project by creating study files, arranges monitoring schedules, leads the project team, organize and run meetings and performs other project management duties as assigned by management
  • Writes Clinical Trial Reports, analyzing and presenting trial results in a clear and accurate format
  • Reports, writes narratives, and follows-up on reported serious adverse events
  • Interacts and attends client meetings, as appropriate
  • Mentors junior staff/CRAs
  • Quality oversight checks of monitoring
  • Performs other duties as assigned

Qualifications
  • Bachelor's degree, or RN, in a related field or equivalent combination of education, training and experience
  • Minimum 5 years' experience as a CRA; experience overseeing clinical trials in the pharmaceutical, hospital or CRO industry
  • Ability to work and travel independently with minimal supervision
  • Experience with numerous EDC systems.
  • Advanced knowledge of GCPs, ICH guidelines, FDA and other applicable regulations
  • Specialized knowledge of CNS therapeutic areas
  • Proficiency in Microsoft Office, Zoom and Adobe
  • Excellent writing and verbal skills, English language proficiency
  • Meticulous attention to detail
  • Time management and ability to prioritize tasks
  • Ability to travel up to 70%

Department Clinical Operations Role Senior Clinical Research Associate Locations Remote, US Remote status Fully Remote Employment type Full-time

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