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Weekend Clinical Trial Educator Jobs (NOW HIRING)

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 ...

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 ...

Prometrika LLC

Clinical Trial Associate II

Cambridge, MA · On-site

$75K - $90K/yr

The Clinical Trial Associate II (CTA II) supports, coordinates, and implements clinical research ... Perform other duties as required EDUCATION * Bachelor's degree in a scientific or health related ...

PTC Therapeutics

Clinical Trial Associate I

Warren, NJ · On-site

$34.75 - $47.50/hr

The Clinical Trial Associate I (CTA) is a key support role within the Clinical Operations ... Minimum level of education and years of relevant work experience. * Bachelor's degree in a relevant ...

Spyglass Pharma

Clinical Trial Associate

Aliso Viejo, CA

$35.50 - $48.50/hr

We are seeking a Clinical Trial Associate (CTA) / Senior CTA to join our team at SpyGlass Pharma ... of education and experience will be considered.) * Some experience in a cross-functional ...

Verastem

Clinical Trial Associate

Boston, MA · On-site

$86K - $100K/yr

... clinical trial processes in accordance with regulatory guidelines and ICH/GCP standards ... education or training, location, and market dynamics. In addition, you will be eligible for an ...

Intuitive

Clinical Trial Manager

Sunnyvale, CA · On-site

The Clinical Trial Manager (CTM) will manage the day-to-day planning and execution of clinical ... Education: Bachelor's degree required in life sciences, biomedical engineering, clinical research ...

Care Access

OR · On-site

Minimum Education: * Bachelor's degree * Minimum Experience: * Must have clinical trial experience. * Must have 5+ years of experience in the clinical trial/pharmaceutical industry. * Must have 2-3+ ...

Prometrika LLC

Clinical Trial Manager

Cambridge, MA · On-site

$140K - $168K/yr

Perform other duties as required EDUCATION * Bachelor's degree in life sciences, nursing, pharmacy ... clinical trial operations * Demonstrated experience managing multiple studies, sites and vendors ...

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Weekend Clinical Trial Educator information

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How much do weekend clinical trial educator jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for weekend 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 cities are hiring for Weekend Clinical Trial Educator jobs? Cities with the most Weekend Clinical Trial Educator job openings:
What are the most commonly searched types of Clinical Trial Educator jobs? The most popular types of Clinical Trial Educator jobs are:
What states have the most Weekend Clinical Trial Educator jobs? States with the most job openings for Weekend Clinical Trial Educator jobs include:
Weekend Clinical Trial Educator jobs near you
Infographic showing various Weekend 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 Associate

Skyhawk Therapeutics

Waltham, MA

$75K - $140K/yr

Full-time

Re-posted 20 days ago

Job description

Clinical Trial Associate/ Senior Clinical Trial Associate

Skyhawk Therapeutics is seeking a highly motivated CTA to provide administrative and operational support to Clinical Operations. 

Responsibilities (including, but not limited to):

  • Organize, participate in, and maintain agendas and meeting minutes for all internal and cross-functional team meetings. Review external meeting minutes as required.
  • Work closely with our clinical operations team to coordinate, track, and manage logistics in support of studies (e.g. review study plans, assist with eTMF reviews).
  • Update and maintain internal trackers (e.g. central enrollment tracker, investigator engagement tracker, bioanalytical sample tracker) and implement updates into ad-hoc presentations and reports as required.
  • Maintain internal Clinical Operations study files and perform periodic reconciliations of documents to ensure all material is present and versioned correctly.
  • Create and maintain study personnel contact lists for all studies and KOLs by disease indication.
  • Assist with the review of study-related documents for clinical studies (e.g. protocol, IB, ICFs).
  • Assist with the facilitation of important external meetings (e.g. Clinical Advisory Board meetings): outreach, scheduling, execution of CDAs and contracts, travel arrangements, presentations, agendas, and minutes.
  • Assist with bioanalytical sample tracking and management of central and third-party labs (sample shipment and analysis timelines).
  • Assist with the review of central and third-party lab documents (e.g. Lab Manual, site flowcharts).
  • Assist with monitoring trip report across the program.

Requirements, Education, Experience & Skills:

  • Relevant education and training required; Bachelor's degree in administrative, science or medical areas of study is a plus.
  • At least 3-5 years of successful administrative experience in biotech/life sciences, health care or clinical study management (title commensurate with experience, with emphasis on eTMF experience)
  • Prefers to contribute as both independent, self-starter, and a collaborative team member.
  • Excellent organizational skills; prefers and can adapt to multiple priorities in a fast-paced and fluid work environment.
  • Excellent verbal and written communication skills.
  • Excellent computer skills, including Microsoft Office Suite: Calendar, Word, Excel, and PowerPoint are essential. SharePoint and SmartSheet preferred.
  • Veeva TMF working knowledge and for senior level, demonstrated knowledge of ICH-GCP, FDA and international regulatory requirements, eTMF management/oversight, and inspection readiness
  • Demonstrated multi-tasking and project management skills.

Skyhawk Therapeutics is committed to pay transparency and equitable compensation practices. The base salary range for the Clinical Trial Associate is $75,000-140,000 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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