ZipRecruiter

Log In

1

Clinical Trial Jobs (NOW HIRING)

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 clinical trials under the direction of the Vice President, Development Operations, with day-to-day ...

Viking Therapeutics

Clinical Trial Manager

San Diego, CA · On-site

$110K - $140K/yr

The Clinical Trials Manager (CTM) will support the conduct of clinical trials and data collection and review, monitoring adherence to protocols, and all activities related to trial completion. The ...

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 clinical trials under the direction of the Vice President, Development Operations, with day-to-day ...

WEP Clinical

Clinical Trial Project Manager

Act as the primary client contact for clinical trial operations, deliverables, and issue resolution. * Lead internal and external meetings, ensuring alignment on project status, risks, and timelines.

Tango Therapeutics

Clinical Trial Leader

Boston, MA · Hybrid

Summary We are seeking a Clinical Trial Leader (CTL) to lead cross-functional clinical trial teams (CTTs) in the execution of clinical trials of Tango's portfolio. This role will chair the CTT and ...

4D Molecular Therapeutics

Clinical Trial Manager

The Clinical Trial Manager will support the Company's clinical trial activities. This position reports to the Director of Clinical Operations. This will be responsible for management of the day to ...

Galderma

Clinical Trial Manager

Boston, MA · On-site

Position Summary The Clinical Trial Manager (CTM) plans and manages overall activities for assigned global clinical trial(s). This includes timelines, budgets, resources, investigational sites ...

Immatics NV

Clinical Trial Manager

$130K - $150K/yr

We are seeking a Clinical Trial Manager (CTM) to support our U.S. Clinical Operations team. The CTM will oversee site management, monitoring oversight, and clinical trial operations activities to ...

next page

Showing results 1-20

All JobsClinical Trial Jobs

Clinical Trial information

See salary details

$28

$62

$96

How much do clinical trial jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for clinical trial in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What qualifications do you need to work in clinical trials?

To work in clinical trials, candidates typically need a relevant educational background such as a bachelor's degree in health sciences, biology, or a related field. Additional qualifications may include experience with Good Clinical Practice (GCP) guidelines, strong organizational skills, and sometimes certifications like Certified Clinical Research Professional (CCRP). Specific roles may require advanced degrees or specialized training depending on responsibilities.

What are clinical trials?

Clinical trials are research studies that involve human participants and are designed to evaluate the safety and effectiveness of new medical treatments, drugs, or devices. These trials follow a carefully controlled protocol and are conducted in phases to systematically assess outcomes. Participants may include patients with specific medical conditions or healthy volunteers, depending on the study's goals. The results from clinical trials help inform medical decisions and regulatory approvals for new therapies.

What are the key skills and qualifications needed to thrive in a Clinical Trial role, and why are they important?

To thrive in a Clinical Trial role, you need a solid understanding of clinical research principles, regulatory compliance, and data management, usually supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Strong attention to detail, organizational abilities, and effective communication skills help professionals coordinate complex processes and collaborate with interdisciplinary teams. These competencies are vital to ensure trials are conducted ethically, efficiently, and in compliance with regulatory standards.

What job makes $10,000 a month without a degree?

In the field of clinical trials, roles such as clinical research coordinators or project managers can earn around $10,000 per month with extensive experience and specialized skills, often without requiring a traditional degree but sometimes needing certifications. These positions typically involve managing trial processes, ensuring compliance, and coordinating between teams, often requiring knowledge of regulatory standards and trial protocols.

What are some common challenges faced by professionals working in clinical trial management, and how can they be addressed?

Professionals in clinical trial management often encounter challenges such as adhering to strict regulatory requirements, managing complex timelines, and ensuring effective communication among multidisciplinary teams. Overcoming these challenges typically involves thorough planning, continuous training on regulatory updates, and the use of project management tools to track progress and coordinate tasks. Building strong relationships with investigators and fostering open communication can also help address issues quickly and maintain trial integrity.

How much money can I make doing clinical trials?

Clinical trial participants can earn anywhere from $50 to $500 per visit, depending on the study's complexity, duration, and location. Compensation varies based on factors such as the type of trial, required procedures, and whether the participant is a healthy volunteer or has a specific condition. Participants often need to meet certain health criteria and may undergo medical assessments before enrollment.

What jobs pay 2000 a day?

In the context of clinical trials, highly specialized roles such as principal investigators, clinical trial consultants, or senior contract research organization (CRO) executives can earn around $2,000 per day, especially for large or complex studies. These positions typically require extensive experience, advanced degrees, and often involve managing trial operations, data analysis, or regulatory compliance.
More about Clinical Trial jobs
What cities are hiring for Clinical Trial jobs? Cities with the most Clinical Trial job openings:
What are the most commonly searched types of Clinical Trial jobs? The most popular types of Clinical Trial jobs are:
What states have the most Clinical Trial jobs? States with the most job openings for Clinical Trial jobs include:
What job categories do people searching Clinical Trial jobs look for? The top searched job categories for Clinical Trial jobs are:
Clinical Trial jobs near you
Infographic showing various Clinical Trial job openings in the United States as of June 2026, with employment types broken down into 21% As Needed, 17% Full Time, 2% Part Time, 2% Temporary, 56% Contract, and 2% Nights. Highlights an 70% Physical, 6% Hybrid, and 24% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Associate

Summit Clinical Research Solutions

San Antonio, TX • On-site

$28.75 - $39.25/hr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Job Title: Clinical Trial Associate

Reports To: PM Manager

Department: Operations

FLSA Status: Exempt

Business Unit: IRO


Summary: The Clinical Trial Associate assists the Summit Project Management team with operational planning, scheduling, and managing of deliverables associated with sponsor protocols and clinical trial sites. The Clinical Trial Associate will work with sponsor requirements utilizing the project specific SOW, protocols, and other data to identify requirements to assist with planning, budgeting, estimating enrollment requirements and forecasting.

The Clinical Trial Associate will work in close collaboration with the Project Management team of SUMMIT


Duties and Responsibilities:


  • Assist in the preparation, handling, distribution, filing, and tracking of clinical documentation and reports
  • Assist in preparation and documentation of internal and external meetings by preparing agendas and minutes
  • Assist in updates for all clinical trials tracking tools
  • Assist in maintaining internal trackers for clinical study activities and study documents
  • Serve as administrative point of contact for internal teams and for external sponsors and CROs
  • Coordinates distribution and shipment of study-related materials
  • Provides general support to the Project Management team on other clinical trial related duties and tasks, as required
  • Maintains central registry of contact information for clinical sites, CROs, vendors and sponsors
  • Assists with the organization of internal team meetings, and other trial-specific meetings
  • Assist with and track Start-up items such as regulatory completion and IRB submission if needed, as well as to provide escalation support for Sponsor, CRO, and sites.
  • Track completion of study set-up items such as Lab kits, IRT, EDC, trainings, SIVs, and vendor qualifications.
  • Other duties as assigned


Qualifications:
  • 2 years of experience in Clinical Research


Knowledge, Skills, and Other Abilities:
  • Ability to synthesize data, with strong attention to detail and accuracy
  • Strong knowledge and understanding of ICH Guidelines, FDA regulations, and GCPs
  • Excellent written and verbal communication skills. Capable of developing precise, accurate written and verbal communications
  • Ability to effectively work across multiple projects, and with multiple organizations in a professional manner
  • Excellent reporting skills
Competencies:

• Excellent written and oral communication skills

• Organizational skills

• Ability to pay attention to detail

• People skills including possessing a positive, friendly, and professional demeanor

• Ability to be flexible with changing priorities

• Ability to communicate in a diplomatic and professional manner

• Strong interpersonal skills

• Strong mathematical knowledge

• Excellent computer skills

• Knowledge of Microsoft Office, internet browsers, and web-based enterprise solutions software.


Work Environment and Physical Demands: The work environment and physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
  • Work may be performed in an office environment.
  • Occasional domestic and/or international travel may be required (20%).