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Remote Informed Consent Action Network Jobs (NOW HIRING)

Ambition 24Hours Inc

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

... informed consent forms, and Clinical Study Reports (CSRs) Prepare regulatory submission documents ... remote environment ───── Ideal Candidate Profile ───── Highly experienced ...

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

... informed consent forms, project management and monitoring plans, vendor study documents ... Support the operational strategy related to assigned vendors, data flow, drug supply, remote ...

Care Access

Travel Sub-Investigator

OR · On-site +1

$46K - $47K/yr

Read and understand the informed consent form, protocol, and investigator's brochure. * Be ... Remote within the United States. This is an on-site mixed with remote tele-medicine work position.

Care Access

Travel Sub-Investigator

$47K - $48K/yr

Read and understand the informed consent form, protocol, and investigator's brochure. * Be ... Remote within the United States. This is an on-site mixed with remote tele-medicine work position.

CrowdStrike

Network Engineer III (Remote)

... open-source network OS #LI-LY1 #LI-Remote This role will require the candidate to periodically ... We support veterans and individuals with disabilities through our affirmative action program.

RDI

Clinical Monitoring Standards Lead

Los Angeles, CA · On-site +1

You will dig into the details: reviewing an individual informed consent, checking source against ... Remote candidates will be considered only if they have a proven method for learning our business ...

Scanhealthplan

Senior Actuarial Analyst - Heath Plan

$90K - $120K/yr

Founded in 1977 as the Senior Care Action Network, SCAN began with a simple but radical idea: that ... Mostly Remote * An annual employee bonus program * Robust Wellness Program * Generous paid-time-off ...

Ad Hoc

Senior Cloud Network Engineer

Mclean, VA · Remote

$105K - $144K/yr

Senior Cloud Network Engineer Job Number: 895 This is a remote position. Ad Hoc is a technology ... for informed decision-making, modernize legacy systems, and build the digital service ...

Veterans Health Administration

Audiologist

Saint Louis, MO · On-site +1

$91K - $119K/yr

May be requested to serve on service-level committees or task forces or to represent to service/section on medical center, network, or national committees * Follows applicable informed consent, HIPAA ...

ICON

Senior Clinical Trial Manager

Blue Bell, PA · On-site +1

When necessary initiates corrective and preventive actions (CAPA) when the trial deviates from ... This includes reviewing and managing site specific informed consent forms in accordance with SOPs ...

DecisionPoint | Cortek

Cloud Network Engineer

These positions are fully remote. Duties & Responsibilities The Cloud Network Engineer will ... EEO and Affirmative Action Policy: DecisionPoint Corporation is an Equal Employment Opportunity and ...

VOLT

Remote Recruiter

Stafford Springs, CT · On-site +1

$60K - $65K/yr

Source, recruit, and staff candidates using job boards, databases, networking, social media, and ... actions. * Monitor staffing levels to maintain required headcount and proactively reduce turnover.

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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.

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Remote Informed Consent Action Network jobs near you
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, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution.

Clinical Trial Manager/Senior Clinical Trial Manager - CNS

Cognitive Research Corporation

Remote

Full-time

Posted 12 days ago

Job description

The Clinical Trial Manager (CTM) is responsible for managing the clinical and operational activities of assigned clinical studies. This is accomplished by ensuring all projects are completed on-time and on-budget while following all company policies, Standard Operating Procedures (SOPs) and applicable regulatory guidelines. Plan, develop, and follow systems and procedures to ensure optimum compliance in accordance with GCP/ICH guidelines and FDA regulations. Ensure operating quality and efficiency.
Essential Duties and Responsibilities
  • Support or lead clinical study activities from start-up through closeout, ensuring adherence to timelines, budget, quality standards, SOPs, and regulatory requirements.
  • Oversee development and maintenance of study documentation including informed consent forms, IRB submissions, project plans, tracking tools, financial worksheets, and regulatory files.
  • Engage with investigative sites during start-up to coordinate CDAs, feasibility assessments, budgets, and CTAs.
  • Manage and maintain the Trial Master File (TMF), ensuring accuracy, completeness, and inspection readiness.
  • Oversee monitoring activities, including review and approval of monitoring visit reports, tracking site issues, data queries, protocol deviations, and ensuring timely resolution.
  • Assign, mentor, and support CRAs; lead team training, provide performance feedback, and ensure ongoing staff compliance with required training.
  • Monitor enrollment trends, operational risks, and study metrics; develop mitigation strategies and escalate issues appropriately.
  • Conduct internal team calls, participate in Sponsor meetings, and serve as key contact for site, CRA, and Sponsor inquiries.
  • Coordinate clinical resource planning, monitoring schedules, and budget oversight related to monitoring activities; support PM with grant administration and invoicing.
  • Participate in development/testing of clinical systems and process improvement initiatives.
  • Perform co‑monitoring visits and, when needed, assume CRA responsibilities.
  • Complete vendor reconciliation and support cross-functional collaboration to ensure data quality.

Qualifications
  • Bachelor's degree or RN in a related field or equivalent combination of education, training and experience
  • Supervisory experience preferred
  • Minimum 3 years' experience in clinical research industry
  • Minimum of 2 years' experience as a Clinical Monitor/Clinical Research Associate (CRA) strongly preferred
  • Working knowledge of GCPs, ICH guidelines, FDA and other applicable regulations
  • Specialized knowledge of CNS therapeutic areas
  • Proficiency in Microsoft Word, Excel, Powerpoint and Outlook
  • Proficiency with Teams and Zoom
  • Effective writing and verbal skills, English language
  • Meticulous attention to detail
  • Time management and ability to prioritize
  • Ability to travel 10-20%

Department Clinical Operations Role Clinical Trial Manager Locations Remote, US Remote status Fully Remote Employment type Full-time

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