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Informed Consent Action Network Jobs (NOW HIRING)

Covenant Health

Clin Research Nurse Coord

Knoxville, TN · On-site

$65K - $82K/yr

Thompson Cancer Survival Center is our region's largest cancer-fighting network, with more imaging ... Maintains federal guidelines for Informed Consent process by communicating information about the ...

Covenant Health

Clin Research Nurse Coord

Knoxville, TN · On-site

$65K - $82K/yr

Thompson Cancer Survival Center is our region's largest cancer-fighting network, with more imaging ... Maintains federal guidelines for Informed Consent process by communicating information about the ...

MedElite Group, LLC.

Consent Coordinator

Hollywood, FL

$20 - $25/hr

By managing a network of advanced practice providers and specialty clinicians, we deliver high ... MedElite is an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate ...

Medasource

Clinical Research Nurse

Winston Salem, NC · On-site

Review study protocols, schedules of events, informed consent forms, and study manuals to ensure ... action items. * Maintain essential regulatory documents and study files. * Collaborate with ...

Carle Health

Research Regulatory Coordinator

Urbana, IL · On-site

$25.81 - $43.10/hr

Performs Informed Consent review and modifies consent form/HIPAA language while working with ... preventive action plans as needed. Updates and maintains current protocol information on the ...

Carle Health

Research Regulatory Coordinator

Urbana, IL · On-site

$24.50 - $32.50/hr

Performs Informed Consent review and modifies consent form/HIPAA language while working with ... preventive action plans as needed. Updates and maintains current protocol information on the ...

Dartmouth-Hitchcock

OBGYN Physician

Bennington, VT · On-site

$250 - $350/hr

Obtain informed consent for treatment, diagnostic, and therapeutic procedures and studies ... affirmative action and equal opportunity employer. All qualified applicants will receive ...

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How much do informed consent action network jobs pay per year?

As of Sep 5, 2026, the average yearly pay for informed consent action network in the United States is $85,999.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,500.00 and $90,500.00 per year, depending on experience, location, and employer.

What is an Informed Consent Action Network?

A job at the Informed Consent Action Network (ICAN) typically involves advocacy, research, and public outreach related to medical freedom and informed consent in healthcare decisions. Employees may work on legal challenges, policy analysis, communications, or community engagement to support ICAN’s mission. Positions can range from legal and regulatory roles to media and research-focused jobs. The organization aims to provide transparency and accountability in public health policies.

What are the typical daily responsibilities for someone working at the Informed Consent Action Network?

Daily responsibilities typically include conducting and reviewing research, developing and updating educational materials, and responding to inquiries from the public or stakeholders regarding informed consent issues. Team members may also coordinate with medical and legal experts, participate in outreach activities, and help organize events or campaigns to raise public awareness. Your work often involves close collaboration with advocacy, communications, and research staff to ensure information is accurate, accessible, and aligned with organizational goals. This role is well-suited for individuals who are detail-oriented and passionate about health communication and patient rights.

What are the key skills and qualifications needed to thrive in the Informed Consent Action Network position, and why are they important?

To thrive in a position at the Informed Consent Action Network, individuals need a solid background in health communications, research, and nonprofit advocacy, often demonstrated with a related degree and relevant experience. Experience with data management tools, content management systems, and compliance with healthcare regulations such as HIPAA is valuable. Outstanding interpersonal skills, adaptability, and the ability to communicate complex information clearly are essential soft skills. These qualifications are important for effectively educating the public, supporting advocacy efforts, and ensuring clear and ethical communication within the organization.

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Informed Consent Action Network jobs near you
Infographic showing various Informed Consent Action Network job openings in the United States as of August 2026, with employment types broken down into 50% Full Time, and 50% Part Time. Highlights an 100% In-person job distribution, with an average salary of $85,999 per year, or $41.3 per hour.

Clinical Research Coordinator

United Urology Group

Scottsdale, AZ • On-site

$24.50 - $32.50/hr

Full-time

Medical, Dental, Vision

Re-posted 9 days ago

Job description

Why Join Us?
At United Urology Group, our employees are at the heart of our mission and have incredible opportunities to impact our patients' lives with their urologic care.
We foster a culture that thrives on compassion, teamwork, integrity, and diversity, all of which start with our staff! We deliver a cohesive approach to urologic care that provides patients with access to experienced specialists, a superb team of healthcare professionals, and the most advanced technology for patient treatments and therapies. We offer competitive salaries and a great work/life balance: enjoy your weekends! UUG offers outstanding benefits, including tuition reimbursement, health, dental, and vision insurance, corporate discounts, and much more!
Job Description:
The Research Coordinator will screen, enroll, and follow study subjects for Phase I, II, III, and IV clinical trials, ensuring protocol compliance and close monitoring while the subjects are on study.
Responsibilities:
Conducting Clinical Trials
  • Review with the Principal Investigator (PI) the inclusion/exclusion criteria, overall structure, and requirements of each protocol and ensure logistics for site implementation.

  • Review the protocol and the informed consent form for accuracy and clarity.

  • Develop and implement strategies for subject recruitment and ongoing communications with all physicians, research staff, and office staff.

  • Complete new trial feasibilities upon review with potential Investigator and submit to Sponsor/CRO. Complete and submit CDA to Sponsor/CRO in accordance with site Standard Operating Procedures (SOP).

  • Schedule site Sponsor visits in accordance with internal SOP.

  • Prepare study charts, binders, and supplies for offsite storage in conjunction with the Regulatory Specialist, when applicable.

  • Ensure maintenance and calibration of site study required equipment.

Enrollment of Study Subjects
  • Review the study design and inclusion/exclusion criteria with the PI/SI, and if needed the Sponsor to ensure understanding.

  • Review, verify, and record/collect all relevant documentation in the subject's medical record needed to confirm study eligibility.

  • Review the protocol, informed consent form, and follow-up procedures with the potential study subjects.

  • Ensure the current approved informed consent is signed before subjects are screened and enrolled.

  • Inform and document notification of the subject's Primary Care Physician of trial participation if approved by the subject.

  • Perform delegated Protocol specific tasks as assigned by Principal Investigator.

  • Ensure that the randomization procedures are followed and documented per protocol guidelines.

  • Document protocol exemptions and deviations, as appropriate. Ensure duplication of each for filing in the subject source and with the regulatory specialist.

  • Ensure all procedures and documentation of subject participation are kept in accordance with FDA regulations, ICH guidance, and internal SOP.

Follow-Up Procedures
  • Schedule subjects for follow-up visits, collect subjects' responses to therapy, and interview subjects for adverse events and changes to concomitant medications. Ensuring that a review of EMR is made during the subject visit for any notable medical/medication changes from the last research visit.

  • Review laboratory data and communicate abnormal values to the PI/SI and as needed, primary care provider or specialist if additional medical attention is needed.

  • Assess and document subject compliance and accountability with Investigational Product (IP). Document re-education when appropriate.

  • Communicate with research staff to ensure timely and accurate study drug distribution when applicable.

  • Administer study drug therapy as needed and maintain the study drug dispensing log if a pharmacist is not involved.
  • Perform venipuncture and collect specimen collection.

  • Record all Adverse Events outlined in protocol and review them with the PI/SI.

  • Report all Serious Adverse Events to the principal investigator, sponsor, and IRB as outlined in the protocol and site SOP. If need be, contact the subject's primary care physician or specialist.

Administrative/Clerical
  • Reporting all Deviations/Adverse/SAE within Sponsor/IRB's timeframe and in accordance with site SOP.

  • Follow SOPs/GCPs/HIPPA according to the site, sponsor, ICH, and FDA.

  • Maintenance of accurate and complete documentation, including but not limited to signed informed consent forms, source documentation, drug dispensing logs, subject logs, and study-related communications.

  • Follow up and document outstanding action items on Monitoring reports, ensure PI/SI oversight, and that the site Regulatory Specialist receives reviewed/corrected/signed copy of the report.

  • File appropriate regulatory or Sponsor communications with the site Regulatory Specialist.

  • Create and maintain Master Subject Log and Visit Log.

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities required of the employee for this job. Duties, responsibilities, and activities may change at any time, with or without notice.
Qualifications:
  • Minimum High School Diploma or GED required.

  • Minimum of two (2) years of clinical research experience.

  • Maintained certification of accreditation (CCRC/IATA/CPR/NIH/CITI) required and will be verified prior to employment.

Key Competencies:
  • Exceptional customer service skills.

  • Strong attention to detail, a willingness to learn & the ability to stay organized.

  • Ability to perform clinical assessments.

  • Strong understanding of FDA clinical trial phases I-IV.

  • Strong understanding of GCP set forth by the ICH.

  • Proficient knowledge of medical terminology.

  • Proficient knowledge of Research-related Terminology.

  • Strong communication skills, both verbal & written.

  • Proficient computer software and database skills.

  • Comfortable working in a fast-paced environment.

  • Very comfortable asking probing questions to patients, if applicable.

  • Must demonstrate a caring, compassionate, and patient attitude.

  • Maintain HIPAA compliance.

  • Multitasking and proactive problem-solving.

  • Ability to type a minimum of 40 words per minute.

Job Type: Full-Time
Actual compensation offered to candidates is based on work experience, education, skill level, and geographic location. Compensation may vary depending on the state or region in which the position is located, in accordance with applicable laws.
This position has no close date. Applications will be accepted until an offer has been extended and accepted.
Equal Opportunity Employer: Our Practice is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability, veteran status, or sexual orientation.
The successful candidate(s) for any UUG position will be subject to a pre-employment background check.

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