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Remote Informed Consent Action Network Jobs (NOW HIRING)

Clinical Research Coordinator III

Carnegie, PA · Remote

$24.75 - $33/hr

Combination of On-Campus or Remote determined by the department. Schedule: Varied based on ... informed consent discussions, assisting with consent issues, and monitoring patients for ...

Also should have experience doing network refresh projects. Non-Negotiable skills would be having ... us informed and involved. Remote work is pretty much the norm here, the team spans across the US.

CRA II

Exton, PA · Remote

$82K - $107K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... IRB approvals, informed consent quality, investigational device accountability, and complete ... corrective actions for protocol deviations across multiple concurrent studies. * Drive ...

CRA II

Exton, PA · Remote

$82K - $107K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... IRB approvals, informed consent quality, investigational device accountability, and complete ... corrective actions for protocol deviations across multiple concurrent studies. * Drive ...

CRA II

Exton, PA · Remote

$82K - $107K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... IRB approvals, informed consent quality, investigational device accountability, and complete ... corrective actions for protocol deviations across multiple concurrent studies. * Drive ...

CRA II

Exton, PA · Remote

$82K - $107K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... IRB approvals, informed consent quality, investigational device accountability, and complete ... corrective actions for protocol deviations across multiple concurrent studies. * Drive ...

CRA II

Exton, PA · Remote

$82K - $107K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... IRB approvals, informed consent quality, investigational device accountability, and complete ... corrective actions for protocol deviations across multiple concurrent studies. * Drive ...

CRA II

Exton, PA · Remote

$82K - $107K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... IRB approvals, informed consent quality, investigational device accountability, and complete ... corrective actions for protocol deviations across multiple concurrent studies. * Drive ...

Cloud Architect - Network (REMOTE)

Washington, DC · On-site +1

$73.25 - $98.25/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... Architect - Network to support KDS and our government customer. The position is remote. This ... actions to maintain service availability and reliability. * Participate in Red Team/Blue Team ...

CRA II

Exton, PA · Remote

$82K - $107K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

... IRB approvals, informed consent quality, investigational device accountability, and complete ... corrective actions for protocol deviations across multiple concurrent studies. * Drive ...

Medical Assistant (2085)

Irving, TX · Remote

$17 - $21.75/hr

Obtain informed consent and enroll eligible patients in remote monitoring programs. * Coordinate the setup and distribution of remote monitoring devices to patients. * Educate patients on how to use ...

Medical Assistant (2466)

Irving, TX · Remote

$17 - $21.75/hr

Obtain informed consent and enroll eligible patients in remote monitoring programs. * Coordinate the setup and distribution of remote monitoring devices to patients. * Educate patients on how to use ...

Network Engineer (LinkedIn recommendation is must) Chicago Illinois 60606 Only W2 candidates Needs ... us informed and involved. Remote work is pretty much the norm here, the team spans across the US.

Network Engineer

Washington, DC · Remote

$140K - $150K/yr

Washington, DC (Remote) Work Schedule: Full-Time | 100% Remote (Occasional On-Site Meetings as ... Participate in root cause analysis and recommend long-term corrective actions. * Collaborate with ...

Network Engineer II

Dallas, TX · On-site +1

$80K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Flexible work options, including remote and hybrid opportunities, if eligible * Retirement Plan ... informed of progress/obstacle. As per the project requirement, configure the Cisco device (Routers ...

Showing results 21-40

Remote Informed Consent Action Network information

What is the difference between Remote Informed Consent Action Network vs Medical Research Coordinator?

AspectRemote Informed Consent Action NetworkMedical Research Coordinator
CredentialsVaries; often includes advocacy or health communication experienceTypically requires clinical research certifications or degrees in health sciences
Work EnvironmentRemote, online advocacy and educationClinical settings, hospitals, or research facilities
Employer & IndustryNonprofit organizations, advocacy groups, health campaignsResearch institutions, hospitals, pharmaceutical companies
Search & Comparison IntentUnderstanding advocacy roles in health consentClinical research management and patient consent processes

The Remote Informed Consent Action Network focuses on advocacy and education related to informed consent, often working remotely for nonprofit organizations. In contrast, Medical Research Coordinators are involved in managing clinical trials and obtaining patient consent in healthcare settings. While both roles involve informed consent, their work environments, credentials, and industry focus differ significantly.

More about Remote Informed Consent Action Network jobs

What cities are hiring for Remote Informed Consent Action Network jobs?

Cities with the most Remote Informed Consent Action Network job openings:

What are the most commonly searched types of Informed Consent Action Network jobs?

The most popular types of Informed Consent Action Network jobs are:

What states have the most Remote Informed Consent Action Network jobs?

States with the most job openings for Remote Informed Consent Action Network jobs include:

Infographic showing various Remote Informed Consent Action Network job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 11% Part Time, and 7% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution.

Clinical Research Coordinator III

System One

Carnegie, PA • Remote

$24.75 - $33/hr

Contractor

Re-posted 29 days ago


Job description

Job Title: Clinical Research Coordinator III Location: Pittsburgh, PA, Hybrid: Combination of On-Campus or Remote determined by the department. Schedule: Varied based on participants schedule Type: Direct Hire or 6 -12 month Contract based on department needs Overview: A top-ranked research university is currently searching for a Clinical Research Coordinator III for one of its growing departments to be for all study-related activities including screening & consent and enrollments, data collection/entry, and compliance with the regulatory process. Responsibilities:
  • Will work closely with the Principal Investigators (PIs), study staff and clinical staff.
  • Responsibilities include but are not limited to screening patients to determine eligibility/verification of enrollments, facilitating study activities, coordinating/conducting informed consent discussions, assisting with consent issues, and monitoring patients for complications and outcomes.
  • Conduct and is responsible for all study-related activities including screening & consent and enrollments, data collection/entry, and compliance with the regulatory process.
  • Encouraged to prepare strategies to improve enrollment/retention. May need to maintain and order supplies as needed.
  • Will Assess protocol feasibility and establish protocol-specific recruitment plans.
  • May be required to train junior staff and oversee the work of others as directed.
  • Will be required to communicate effectively with study participants and potential community recruits.
  • Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols.
  • Recruits research subjects and conducts interviews and research assessments.
Requirements:
  • Minimum Education Requirement: Bachelor’s Degree
  • Experience Requirement: At least 3-5 years of clinical trial/clinical research experience within industry/sponsor trials
  • Education/Experience Substitution: A combination of relevant education and experience will be considered in place of the specified educational and/or experience requirements.
  • Preferred Certification: CRC certification is preferred but not required.

#M3

Ref: #558-Scientific