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Weekend Clinical Trial Educator Jobs (NOW HIRING)

IQVIA

Clinical Trial Rater

Atlanta, GA · 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

Durham, 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

Houston, TX · 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

New York, NY · 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

Boston, 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 ...

IQVIA

Clinical Trial Rater

Chicago, IL · 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

New Providence, NJ · 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

Dallas, TX · 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

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 ...

Coloplast

Clinical Trial Administrator

Minneapolis, MN · On-site

$65 - $85/hr

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 ...

New

Aerogen

Clinical Trial Manager

Morrisville, NC · On-site

$90 - $120/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 ...

New

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

As of Sep 2, 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.

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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, 72% Full Time, 18% Part Time, and 7% 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

Kailera Therapeutics, Inc.

Waltham, MA • On-site

Full-time

Posted 29 days ago

Job description

What You'll Do:

The Clinical Trial Manager will provide project support to team members by leading and/or participating in the daily management of clinical trial activities. Successful candidate will be working closely with and will be responsible for oversight of study activities through our CROs and service providers, including study start-up, conduct, and completion.
This position provides an opportunity to join a rapidly growing Clinical Operations organization and contribute substantially to the building of the department and the successful implementation of trials. 

Required location: Waltham, MA (hub-based, onsite 3-4 days per week)

Responsibilities:

  • Perform as the lead interface with the CRO regarding status of project activities and deliverables (including but not limited to site identification and selection, pre-study activities, enrollment, management/conduct, database lock, post-study activities)
  • Collaborate with the cross-functional clinical trial team to review and prepare various clinical study documents including but not limited to study protocol, model informed consent forms, and study plans
  • Lead day-to-day management of external vendors, as needed, to support the trial design and implementation
  • Review and approve internal and external vendor study plans and processes, as applicable
  • Review monitoring reports and interact with CRO to ensure the quality of monitoring and site management
  • Work with cross-functional team to ensure data query management and data retrieval is taking place in a timely manner
  • Review deviation listings and site audit reports and work with team to resolve site issues (e.g., staff retraining, additional resources)
  • Maintain and ensure the quality and completeness of study master files in compliance with GCP
  • Lead Clinical Study Team meetings internally, and/or with CRO and service providers

Required Qualifications:

  • Work experience to include a minimum of 6 years clinical trial experience with a solid understanding of functional area responsibilities associated with the clinical development process
  • Good working knowledge of ICH-GCP guidelines and regulatory requirements for clinical trial management
  • Must have strong clinical study management, communication (oral and written), and analytical skills
  • Excellent interpersonal skills, with a demonstrated ability to work in a team environment as well as independently
  • Additional attributes include an ability to multi-task, be flexible, and to thrive in a fast-paced environment
  • Demonstrated ability to effectively manage external vendors & CROs
  • Advanced proficiency in Microsoft Office and Microsoft Project or other Project Management software
  • Demonstrated strong written and verbal communication skills
  • Must be able to travel 

 

Education:

  • BA/BS; Life Science degree a plus

Apply