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Patient Informed Consent Specialist Jobs (NOW HIRING)

Site Start-Up Specialist based in Switzerland

$35.50 - $47.75/hr

As a Site Start-Up Specialist (location: Switzerland, Home-based), you will play a pivotal role in ... Ability to review and adapt patient informed consent forms to meet local and protocol-specific ...

MN · On-site

$40 - $41/hr

Experience managing Patient Informed Consent documentation within the US * Strong document management and adherence to standard operating procedures * Ability to work with cross-functional teams and ...

RN Anesthesia

Hays, KS · On-site

$30 - $46/hr

... patient informed consent. * Analyzes all patients schedule for surgery and ensures all medical and cardiac clearance are ordered and reviewed. * Follows approved anesthesia protocols in regards to ...

... patient informed consent. * Analyzes all patients schedule for surgery and ensures all medical and cardiac clearance are ordered and reviewed. * Follows approved anesthesia protocols in regards to ...

... patient informed consent. * Analyzes all patients schedule for surgery and ensures all medical and cardiac clearance are ordered and reviewed. * Follows approved anesthesia protocols in regards to ...

Oncology Patient Navigator

Austin, TX · On-site

$150 - $250/hr

The Oncology Patient Navigator is a patient-facing support role within a structured clinical trial ... physician informed-consent counseling. • Conducting the study site's informed consent session ...

Conducting the study site's informed consent session. * Creating verbatim conversation transcripts or storing non-relevant patient information. What We're Looking For * Qualified oncologist (MD or ...

... patient informed consent when indicated. * Documents and communicates all required components of patient care. Qualifications: Required: * High School Diploma or GED * BLS Certification * Licensed ...

RN

Hays, KS · On-site

$25 - $36/hr

... verifies patient informed consent when indicated. * Documents and communicates all required components of patient care. * Provides direct patient care in the inpatient Med/Surg setting.

RN

Hays, KS · On-site

$25 - $36/hr

... verifies patient informed consent when indicated. * Documents and communicates all required components of patient care. * Provides direct patient care in the inpatient Med/Surg setting.

RN

Hays, KS · On-site

... verifies patient informed consent when indicated. * Documents and communicates all required components of patient care. * Provides direct patient care in the inpatient Med/Surg setting.

RN

Hays, KS · On-site

... verifies patient informed consent when indicated. * Documents and communicates all required components of patient care. * Provides direct patient care in the inpatient Med/Surg setting.

RN

Hays, KS · On-site

... verifies patient informed consent when indicated. * Documents and communicates all required components of patient care. * Provides direct patient care in the inpatient Med/Surg setting.

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Patient Informed Consent Specialist information

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How much do patient informed consent specialist jobs pay per hour?

As of Aug 31, 2026, the average hourly pay for patient informed consent specialist in the United States is $21.56, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $22.12 per hour, depending on experience, location, and employer.

What is a patient informed consent specialist?

A Patient Informed Consent Specialist is a healthcare professional responsible for ensuring that patients fully understand the details, risks, and benefits of clinical trials or medical procedures before agreeing to participate. They explain complex medical information in a clear and compassionate way, answer patients’ questions, and document the consent process. Their role helps protect patient rights and ensures legal and ethical compliance in healthcare settings, particularly in research and clinical trials.

What skills and qualifications are needed to be a patient informed consent specialist?

To thrive as a Patient Informed Consent Specialist, you need a solid understanding of clinical research protocols, regulatory requirements, and patient privacy laws, typically supported by a degree in health sciences or a related field. Familiarity with electronic consent management systems, clinical trial databases, and compliance software is commonly required. Outstanding communication, attention to detail, and cultural sensitivity are crucial soft skills for effectively educating patients and ensuring ethical practices. These skills ensure patients are fully informed, protected, and able to make voluntary decisions regarding their participation in clinical studies.

What challenges do patient informed consent specialists face during the consent process, and how are they addressed?

Patient Informed Consent Specialists often encounter challenges such as language barriers, varying levels of health literacy, and patient anxiety or misunderstanding about medical procedures. To address these, specialists use clear, plain language, provide translated materials, and employ visual aids or interpreters when necessary. They also dedicate time to answer patient questions and collaborate closely with clinical staff to ensure patients fully understand their rights and the details of the study or procedure. This thorough approach helps build trust and ensures ethical standards are met throughout the consent process.

What is the difference between Patient Informed Consent Specialist vs Medical Records Technician?

AspectPatient Informed Consent SpecialistMedical Records Technician
CredentialsTypically requires healthcare-related certifications or training in patient communicationPost-secondary education, often a certificate or associate degree in health information management
Work EnvironmentHospitals, clinics, or healthcare facilities focusing on patient communication and consent processesMedical record departments, handling patient data and health information documentation
Employer & Industry UsageHealthcare providers, hospitals, clinicsHealthcare facilities, insurance companies, medical offices
Search & Comparison IntentUnderstanding roles related to patient consent and communicationManaging and organizing medical records and health information

The Patient Informed Consent Specialist focuses on ensuring patients understand and sign consent forms, emphasizing communication and compliance. In contrast, the Medical Records Technician manages and maintains patient health records, focusing on data accuracy and confidentiality. While both roles are vital in healthcare settings, they serve distinct functions related to patient information and documentation.

More about Patient Informed Consent Specialist jobs

What cities are hiring for Patient Informed Consent Specialist jobs?

Cities with the most Patient Informed Consent Specialist job openings:

What states have the most Patient Informed Consent Specialist jobs?

States with the most job openings for Patient Informed Consent Specialist jobs include:

Infographic showing various Patient Informed Consent Specialist job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 73% Full Time, 16% Part Time, and 8% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $44,844 per year, or $21.6 per hour.

Site Start-Up Specialist based in Switzerland

Remote


Fortrea
Health Care and Social Assistance • 10K+ employees

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

27th of 74 rated research

People enjoy working here

Good employer

Respectful managers


$35.50 - $47.75/hr

Other

Re-posted 7 days ago


Job description

Join Our Team and Drive Clinical Research Success!

At Fortrea, we are committed to accelerating clinical trials and ensuring regulatory compliance. As a Site Start-Up Specialist (location: Switzerland, Home-based), you will play a pivotal role in coordinating site start-up activities, managing essential documents, and ensuring regulatory submissions are completed efficiently. Your expertise will help bring life-changing treatments to patients faster.

In this role, you will be part of our FSPx team and work directly with one of our renowned key sponsor to advance the development of innovative, life-changing medications.

Key Responsibilities

In this role, you will:

  • Serve as the primary contact for investigative sites during start-up and maintenance activities.
  • Collect, review, and organize essential documents required for regulatory submissions (EC/IRB/Third Body/Regulatory Authority).
  • Ensure compliance with ICH/GCP guidelines, regulatory requirements, and sponsor specifications.
  • Prepare and submit regulatory documents, including country-specific application forms and informed consent forms.
  • Track submission timelines and proactively address potential delays.
  • Collaborate with internal and external stakeholders, including vendors, clinical teams, and regulatory authorities.
  • Ensure all documentation is audit-ready and systems are consistently updated.
  • Assist in the negotiation of site contracts and budgets, if applicable.
  • Provide mentorship and training to new hires and less-experienced colleagues.
Required Qualifications

To succeed in this role, you should have:

  • University/College degree (life sciences preferred) or certification in a related allied health profession.
  • Minimum 2 years of experience in clinical research, regulatory submissions, or site activation.
  • Strong knowledge of ICH/GCP guidelines, RA, IRB/IEC regulations, and start-up processes.
  • Ability to review and adapt patient informed consent forms to meet local and protocol-specific requirements.
  • Experience interacting with regulatory authorities and site start-up teams.
  • Excellent organizational, problem-solving, and communication skills.
  • Proficiency in Microsoft Office and document management systems.
  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
What We Offer
  • Competitive salary and performance-based incentives.
  • Flexible work arrangements (remote/hybrid options).
  • Professional growth opportunities in a collaborative and innovative environment.
  • The opportunity to work on cutting-edge clinical research projects.

Ready to Make an Impact?

Join us in shaping the future of clinical research. Apply today!

Applications are reviewed on a rolling basis—don't miss this opportunity!



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