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Clinical Trial Educator Jobs (NOW HIRING)

IQVIA

Clinical Trial Rater

Raleigh, NC · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign ...

IQVIA

Clinical Trial Rater

Washington, DC · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign ...

IQVIA

Clinical Trial Rater

Springfield, MA · Remote

Clinical Trial Rater - Borderline Personality Disorder (BPD) Location: Remote based in the US Hours ... Education: PhD or PsyD (Psychology, Psychiatry, Health Sciences), Medical Doctor (MD), Foreign ...

Aerogen

Clinical Trial Manager

Morrisville, NC · On-site

$100 - $125/hr

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials ... Education and Experience * RT, RN, or Bachelor's degree in a related field or equivalent ...

Skyhawk Therapeutics

Clinical Trial Manager

Waltham, MA · On-site

$140K - $200K/yr

Clinical Trial Manager Skyhawk Therapeutics seeks an experienced Clinical Trial Manager (title ... Education, Experience & Skills: * Bachelor's degree, or equivalent, in a biomedical, life science ...

Coloplast

Clinical Trial Administrator

Minneapolis, MN · On-site

$65K - $85K/yr

The Clinical Trial Administrator (CTA) fulfils a specialized research role within the Clinical ... Experience managing device or pharmacology trials or evidence of experience/education in clinical ...

Predicine, Inc

Clinical Trial Associate

Hayward, CA · On-site

$38.50 - $52.50/hr

... Education Bachelor's degree in biology, Life Sciences, or related field required; Associate degree in health science field may be considered with relevant clinical trial experience. Advanced degree ...

Verastem

Clinical Trial Manager

Boston, MA · On-site

$100K - $125K/yr

Summary: We are seeking a Clinical Trial Manager with experience in managing a global Phase 3 ... education or training, location, and market dynamics. In addition, you will be eligible for an ...

IQVIA

Clinical Trial Lead

Durham, NC · On-site +1

An education as a physician would be a plus. Minimum of 5 years (or 10 years for Senior CTL role ... clinical operations and trial management with leading a clinical team in a matrix structure ...

Intuitive

Clinical Trial Assistant

Sunnyvale, CA · On-site

$70K - $94K/yr

Research/clinical trial management certification/ education is a plus * Able to travel up to 10% * We provide market-competitive compensation packages, inclusive of base pay, incentives, benefits and ...

IQVIA, Inc.

Clinical Trial Lead

Durham, NC · On-site

An education as a physician would be a plus. • Minimum of 5 years (or 10 years for Senior CTL ... clinical operations and trial management with leading a clinical team in a matrix structure ...

Galderma

Senior Clinical Trial Manager

Boston, MA · On-site

$110K - $135K/yr

The Opportunity The Senior Clinical Trial Manager (CTM) plans and manages overall activities for ... education, certifications, location and applicable geographic pay zones, market conditions ...

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Clinical Trial Educator information

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How much do clinical trial educator jobs pay per hour?

As of Sep 7, 2026, the average hourly pay for clinical trial educator in the United States is $43.95, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $52.40 per hour, depending on experience, location, and employer.

What is a clinical trial educator?

A Clinical Trial Educator (CTE) is a healthcare professional who educates and supports clinical trial sites, patients, and healthcare providers to increase awareness and understanding of clinical studies. They work to improve patient recruitment and retention by providing information on trial protocols, procedures, and potential benefits. CTEs collaborate with investigators and site staff to ensure compliance with study requirements and enhance study execution. Their role helps bridge the gap between clinical research teams and participants, ultimately contributing to the success of clinical trials.

What are the typical daily responsibilities of a clinical trial educator?

A Clinical Trial Educator typically delivers training and support to clinical site staff on study protocols, procedures, and regulatory compliance, both in person and virtually. They regularly assess and address knowledge gaps, answer site staff questions, and help resolve protocol deviations to ensure consistent trial conduct. Collaboration with clinical research associates, trial managers, and sponsor representatives is common, as is maintaining accurate documentation of training activities. This role requires strong organizational skills to balance multiple sites and studies simultaneously, making adaptability and clear communication especially important for success.

What are the key skills and qualifications needed to thrive in the clinical trial educator position, and why are they important?

To thrive as a Clinical Trial Educator, you need a strong background in clinical research, a relevant healthcare or life sciences degree, and comprehensive knowledge of clinical trial protocols and regulatory requirements. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is highly valuable. Exceptional communication, presentation skills, and the ability to educate and motivate clinical staff are key soft skills in this role. These capabilities are critical for ensuring protocol adherence, effective trial site performance, and successful participant engagement throughout the study.

How do you become a clinical trial educator?

To become a clinical trial educator, individuals typically need a background in healthcare, life sciences, or a related field, along with strong communication skills. Relevant experience may include working in clinical research, patient education, or training roles, and certifications such as Good Clinical Practice (GCP) can enhance qualifications.

How much do clinical trial educators make?

Clinical trial educators typically earn between $60,000 and $90,000 annually, depending on experience, location, and employer. Salaries can vary based on certifications, such as GCP or CRA, and the complexity of the trials they oversee.
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Clinical Trial Educator jobs near you
Infographic showing various Clinical Trial Educator job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $91,418 per year, or $44 per hour.

Clinical Trial Manager

Skyhawk Therapeutics

Waltham, MA • On-site, Remote

$140K - $200K/yr

Full-time

Posted 11 days ago

Key responsibilities

  • Manage execution of the clinical study in compliance with applicable regulations and SOPs.

  • Develop, manage, and maintain study deliverables through collaboration with internal and external stakeholders.

  • Assist in managing CRO and vendor activities to ensure timely and on-budget delivery of trial objectives.

Job description

Clinical Trial Manager

Skyhawk Therapeutics seeks an experienced Clinical Trial Manager (title commensurate with experience) who is looking to work in a fast paced, growth mindset organization focused on developing innovative therapies across a broad portfolio of development candidates. Skyhawk's preferred candidate will have Clinical Operations experience preferably supporting rare or CNS trials in a biotech/small pharma setting to join our Clinical Operations group.

Responsibilities:

  • Manage execution of the clinical study in compliance with ICH/GCP, Regulatory Authorities' regulations/guidelines, and applicable SOPs/Work Instructions
  • Development, management, maintenance of study deliverables [i.e. protocols, informed consents, timelines, study plans, etc.] through collaboration with internal and external stakeholders
  • Participation in Vendor and system selection (as applicable), specification development, and management/oversight of key trial vendor/system deliverables, including developing and managing to contracts and budgets
  • Management of study training for study team, investigational sites, and vendors in collaboration with medical and scientific colleagues
  • Contribute to cross functional deliverables across the study team internally. Ensuring timely information sharing and inclusion of relevant expertise areas to deliver trial results on time, efficiently and effectively
  • Assist in managing CRO and other study vendors day-to-day activities working directly with the CRO or vendor trial management team, ensuring contracted deliverables are achieved on time and on budget
  • Contribute to development of proactive strategy to enable timely delivery of study objectives, including but not limited to enrollment projections, cohort planning, identification of potential challenges in study execution and risk management
  • Ensure execution of study in a GxP compliant manner by working closely with QA to develop (as applicable) corrective and preventive action plans (CAPAs) to address trial issues in collaboration with cross functional team
  • Responsible for supporting the management, oversight and maintenance of the Trial Master File (TMF)
  • Contribute to growth and development of clinical operations function via process/SOP review and process improvement initiatives

Requirements, Education, Experience & Skills:

  • Bachelor's degree, or equivalent, in a biomedical, life science or related field of study
  • Minimum of 5+ years of progressively increasing Clinical Operations experience within the biotech/pharma industry; Rare disease or CNS experience preferred (title commensurate with experience)
  • Strong understanding of Global regulatory and ICH-GCP compliance requirements for clinical research
  • Solid teamwork, organizational, interpersonal, and problem-solving skills
  • Ability to influence and collaborate well with colleagues and partners in a fast-paced environment
  • Proven track record (>2 years) of successful remote work in clinical operations if unable to be onsite
  • Ability and willingness to travel up to 25% of time

Skyhawk Therapeutics is committed to pay transparency and equitable compensation practices. The base salary range for the Clinical Trial Manager is $140,000-200,000 annually. This range reflects the minimum and maximum target for such position. Skyhawk Therapeutics will assess the appropriate level for a qualified candidate based on job-related skills, professional experience, and relevant education or training.

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