1

Informed Consent Action Network Jobs (NOW HIRING)

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 ...

Coordinate updates related to study protocols, informed consent forms, investigators, and ... Coordinate meetings, develop agendas, generate meeting minutes, and track action items. * Develop ...

Coordinate updates related to study protocols, informed consent forms, investigators, and ... Coordinate meetings, develop agendas, generate meeting minutes, and track action items. * Develop ...

... informed consent process alongside study staff -- Demonstrates professionalism and collegiality through actions, interactions, and communications with others appropriate to an environment that is ...

... informed consent process alongside study staff -- Demonstrates professionalism and collegiality through actions, interactions, and communications with others appropriate to an environment that is ...

City of Hope's growing national system includes its Los Angeles campus, a network of clinical care ... Responsibilities include patient recruitment, informed consent, trial coordination, data management ...

City of Hope's growing national system includes its Los Angeles campus, a network of clinical care ... Responsibilities include patient recruitment, informed consent, trial coordination, data management ...

City of Hope's growing national system includes its Los Angeles campus, a network of clinical care ... Responsibilities include patient recruitment, informed consent, trial coordination, data management ...

City of Hope's growing national system includes its Los Angeles campus, a network of clinical care ... Responsibilities include patient recruitment, informed consent, trial coordination, data management ...

City of Hope's growing national system includes its Los Angeles campus, a network of clinical care ... Responsibilities include patient recruitment, informed consent, trial coordination, data management ...

Showing results 41-60

Informed Consent Action Network information

See salary details

$76.5K

$86K

$94K

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

As of Aug 13, 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 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.

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 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.

More about Informed Consent Action Network jobs

What cities are hiring for Informed Consent Action Network jobs?

Cities with the most 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 Informed Consent Action Network jobs?

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

What job categories do people searching Informed Consent Action Network jobs look for?

The top searched job categories for Informed Consent Action Network jobs are:

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

Research Regulatory Coordinator

Carle Health

Urbana, IL • On-site

$25.81 - $43.10/hr

Full-time

Re-posted 11 days ago


Carle Health rating

7.5

Company rating: 7.5 out of 10

Based on 213 frontline employees who took The Breakroom Quiz

234th of 887 rated healthcare providers


Job description

Overview
The Clinical Research Regulatory Coordinator is a specialized research professional that facilitates and coordinates the regulatory aspects of a clinical trial and plays a critical role in the conduct of research at Carle. This role is responsible for preparing, completing, and submitting required forms and documents, in consultation with the research team, to meet regulatory, IRB, and HIPAA guidelines and policies, at the time of initial review, modifications, and continuing review. The Clinical Research Regulatory Coordinator performs Informed Consent review and modifies consent form/HIPAA language while working with sponsors and IRBs for all studies to conform to Carle institutional guidelines.
Responsibilities
Prepares, completes, and submits required forms and documents, in consultation with the research team, to meet regulatory, IRB, and HIPAA guidelines and policies, at the time of initial review, modifications, and continuing review.
Performs Informed Consent review and modifies consent form/HIPAA language while working with sponsors and IRBs for all studies to conform to Carle institutional guidelines. Ensures consent language matches the research contract, budget, and protocol.
Completes, submits, and maintains regulatory documents as applicable (including 1572s, Delegation of Authority logs, Financial Disclosure Forms, Consent Forms, and trainings) for industry sponsored as required.
Prepares for and participates in external sponsor/monitor visits. Prepares for and participates in internal/external audits to ensure regulatory compliance and implement corrective and preventive action plans as needed.
Updates and maintains current protocol information on the Research website. Distributes protocol documents to appropriate researcher and PI for review, approval, and implementation.
Tracks study approvals and expirations to ensure uninterrupted project approval. Maintains regulatory database and manages electronic filing of all regulatory documents.
Creates, submits, and maintains complete documentation to comply with research base regulatory requirements for oncology federally funded research projects
Trains/assists new/seasoned Staff on regulatory process including CITI training, Study start-up, IRB submissions, maintaining a Study, and ensuring all essential documents are correct to submit to monitor/sponsor.
Advises on remedies and revisions, in collaboration with the coordinator and/or investigator, and resolves any procedural issues that might arise in order to ensure timely IRB review
Updates and maintains the active informed consent documents and HIPAA authorizations that are being utilized in projects in which subjects are consented (whether Carle research is assisting with consenting or not)
Notifies appropriate staff, physicians, investigators and affiliates of protocol activations and closures in a timely manner
Facilitates study closure in collaboration with investigator, research coordinator, and sponsor
Applies rules and regulations (Carle local, state, federal, industry, sponsor, etc.), in collaboration with the Sr Clinical Research Regulatory Coordinator, and recommends and guides principal investigators (PIs) and research staff in the creation, submission, documenting, reporting, etc. of study activities ensuring appropriate compliance
Monitors Investigator Initiated IRB-deferred studies, exempt and non-engaged projects for by ensuring regulatory documentation is current and maintained , including any IRB approvals
Qualifications
Certifications: Certified Clinical Research Professional (CCRP) within 3 years - Society of Clinical Research Associates (SOCRA)Society of Clinical Research Associates (SOCRA), Education: Experience In Lieu of Education: Related Field; Bachelor's Degree: Related Field, Work Experience: Related field
Carle Health Company Overview
Find it here.
Discover the job, the career, the purpose you were meant for. At Carle Health, we're committed to fostering a workplace where every team member feels valued, respected and empowered, where passion and purpose come together to positively impact the lives of our patients and our communities. Find it all at Carle Health.
Our nearly 17,000 team members and providers work together to support patient care across central and southeastern Illinois. We've grown to include eight, award-winning hospitals and a multispecialty provider group with more than 1,500 doctors and advanced practice providers. We're developing the next generation of providers and healthcare professionals through Carle Illinois College of Medicine, the world's first engineering-based medical school, and Methodist College. Carle BroMenn Medical Center, Carle Foundation Hospital, Carle Health Methodist Hospital, Carle Health Proctor Hospital, Carle Health Pekin Hospital, and Carle Hoopeston Regional Health Center hold Magnet® designations, the nation's highest honor for nursing care. We offer opportunities in several communities throughout central Illinois with potential for growth and life-long careers at Carle Health.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class. Carle Health participates in E-Verify and may provide the Social Security Administration and, if necessary, the Department of Homeland Security with information from each new employee's Form I-9 to confirm work authorization. | For more information: human.resources@carle.com.
Salary Range
The compensation range for this position is $25.81per hour - $43.1per hour. This represents a good faith minimum and maximum range for the role at the time of posting by Carle Health. The actual compensation offered a candidate will be dependent on a variety of factors including, but not limited to, the candidate's experience, qualifications, location, training, licenses, shifts worked and compensation model.
Carle Health offers a comprehensive benefits package for team members and providers. To learn more visit careers.carlehealth.org/benefits.

What Carle Health employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


Carle logo

About Carle

Sourced by ZipRecruiter

Each and every employee at Carle makes us better and stronger, so we can take care of our patients and our community. From clinical to professional and technical careers – our team of employees help us change lives. Carle is proud to be named a Great Place to Work®. Alongside Carle BroMenn Medical Center, Carle Health Methodist Hospital, and Carle Health Proctor Hospital, the Carle Foundation Hospital holds Magnet® designation, the nation’s highest honor for nursing care.

Industry

Health care and social assistance and hospitals

Company size

10,000+ Employees

Headquarters location

Urbana, IL, US