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Assistant Clinical Trial Monitor Jobs (NOW HIRING)

Socket.dev

Sr./Clinical Trial Manager

San Diego, CA · On-site

$120 - $150/hr

... monitoring adherence to protocols, and all activities related to trial completion. The Sr./CTM ... CRO Selection: Assist with review of proposals from CROs, review CROs' SOPs, prepare and recommend ...

New

Viking Therapeutics

Sr./Clinical Trial Manager

San Diego, CA · On-site

$120K - $150K/yr

... monitoring adherence to protocols, and all activities related to trial completion. The Sr./CTM ... CRO Selection: Assist with review of proposals from CROs, review CROs' SOPs, prepare and recommend ...

Icon plc

Clinical Trial Assistant

San Francisco, CA · Hybrid

$56K - $70K/yr

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... Support oversight of monitoring visit report review. Activities include updating MVR trackers and ...

Icon plc

Clinical Trial Assistant

San Francisco, CA · Hybrid

$56K - $70K/yr

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... Support oversight of monitoring visit report review. Activities include updating MVR trackers and ...

ICON

Clinical Trial Assistant

San Francisco, CA · On-site

$56K - $70K/yr

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical ... Support oversight of monitoring visit report review. Activities include updating MVR trackers and ...

Cellectis

Clinical Trial Associate

Manhattan, NY · On-site

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... * Assist with review of monitoring visit reports (initiation, routine monitoring, and close-out ...

Cellectis

Clinical Trial Associate

Manhattan, NY

$36.75 - $50.25/hr

The Clinical Trial Associate (CTA) supports clinical study teams in the execution and oversight of ... * Assist with review of monitoring visit reports (initiation, routine monitoring, and close-out ...

Ardelyx

Clinical Trial Associate

Newark, CA · On-site

$86 - $105/hr

Provide operational support for assigned clinical trial(s) across all phases of the study lifecycle, including start‑up, conduct and close‑out activities. * Assist Clinical Trial Managers (CTMs ...

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Assistant Clinical Trial Monitor information

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$37

$68

How much do assistant clinical trial monitor jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for assistant clinical trial monitor in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What is the difference between Assistant Clinical Trial Monitor vs Clinical Trial Monitor?

AspectAssistant Clinical Trial MonitorClinical Trial Monitor
CredentialsOften requires a bachelor's degree in life sciences or related field; certifications like SOCRA or ACRP are commonTypically requires similar degrees and certifications, with more experience
Work EnvironmentSupports monitoring activities under supervision, often in office or site settingsLeads monitoring visits, oversees site compliance, and makes independent assessments
ResponsibilitiesAssists with data collection, site communication, and documentationPerforms site visits, verifies data accuracy, and ensures protocol adherence

The main difference is that the Assistant Clinical Trial Monitor supports and assists in monitoring activities, often under supervision, while the Clinical Trial Monitor takes on more independent responsibilities, leading site visits and ensuring compliance. Both roles require similar credentials and work in comparable environments, but the level of responsibility distinguishes them.

What cities are hiring for Assistant Clinical Trial Monitor jobs?

Cities with the most Assistant Clinical Trial Monitor job openings:

What are the most commonly searched types of Clinical Trial Monitor jobs?

The most popular types of Clinical Trial Monitor jobs are:

What states have the most Assistant Clinical Trial Monitor jobs?

States with the most job openings for Assistant Clinical Trial Monitor jobs include:

Assistant Clinical Trial Monitor jobs near you
Infographic showing various Assistant Clinical Trial Monitor job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, 1% Temporary, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $78,347 per year, or $37.7 per hour.

Assistant Clinical Trial Navigator

Javara

Savannah, GA • On-site

Full-time

Posted 8 days ago

Job description

Job Description:
As an Assistant Clinical Trial Navigator with Javara, you will assist with the coordination and administration of clinical trials and report to the Manager of Site Operations and the Principal Investigator or designee. You will participate in achieving and exceeding patient enrollment goals with a dedication to quality and integrity. With a guiding principle of research participant safety, you will assist with implementing and coordinating research study procedures for the successful management of clinical trials.
Essential Responsibilities:
  • Seek to improve the patient's experience, never compromising on safety.
  • Provide excellent customer service to patients and participants, healthcare partner and practice stat investigators, sponsors, and vendors.
  • Support enrollment goals by contributing to enrollment strategies, striving to provide exceptional experiences for patients, and building relationships with local patient populations.
  • Assist with patient identification and recruitment as needed.
  • Assist in strengthening efficient working relationships with colleagues, patients, investigators, and other internal and external partners.
  • Ensure scientific integrity of data and record source data appropriately and accurately inclusive of patient visit data within source, CTMS, electronic reporting systems, completing the sponsor's case report form, and timely query resolution.
  • Assist with ensuring study documentation is up to date and audit ready.
  • Adhere to all Standard Operating Procedures (SOPs), Good Clinical Practices (GCPs), protocols, OSHA, proper PPE usage and other regulatory authority requirements.
  • Assist with conducting and documenting the informed consent process.
  • Demonstrate continuous commitment to learning and developing skill sets and knowledge base as it relates to clinical trial operations and the patient experience.
  • Coordinate and schedule patient visits and conduct visits per protocols.
  • Assist with performing clinical and laboratory skills such as therapeutic area specifics, obtaining vitals, EKGs, and collecting, processing, and shipping bodily samples.
  • Demonstrate our Core Values such as fostering teamwork and collaboration and cultivating relationships with healthcare system representatives.
  • Additional tasks as assigned.

Qualifications:
  • Associates or Bachelor's Degree in related field or equivalent experience highly beneficial.

Work Environment:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job.
  • This job operates in a professional environment.
  • The noise level in this work environment is usually light to moderate.

Physical Demands:
The physical demands described here are representative of those that must be met to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this job.
  • The employee will regularly use hands to reach, handle or feel objects, tools, or controls and talk and hear.
  • The employee may frequently stand, walk and sit.
  • The employee may occasionally lift and/or move up to 25 pounds.
  • Specific vision abilities required include close vision, distance vision and the ability to adjust focus.

Travel: This position may require up to 30% travel regionally but may occasionally include travel to other regions or Javara headquarters in Winston-Salem, NC.
Pre-Employment Screening: Drug screen and background check required.
This job description covers the most essential functions of this position and is not designed to contain a comprehensive listing of activities, duties or responsibilities that are required of the employee in this job. Duties, responsibilities, and activities may change at any time with or without notice.
Javara is an integrated research organization (IRO) that advances value by integrating clinical research within the healthcare ecosystem. Javara brings better outcomes for patient centered care, better economic results, improved access to cutting edge therapies and a more predictable research delivery model to the biopharmaceutical sector.
Equal Employment Opportunity Statement: Javara provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

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