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 ...

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 ...

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 ...

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 ...

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 ...

Icon plc

Clinical Trial Manager

Blue Bell, PA

As a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programmes.

Tango Therapeutics

Clinical Trial Leader

Boston, MA · On-site

$160K - $241K/yr

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 ...

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 16, 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

Clinical Trial Associate

Repertoire Immune Medicines

Cambridge, MA • On-site

$36.50 - $49.75/hr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 18 days ago

Job description

Repertoire Immune Medicines is a clinical-stage biotechnology company harnessing the power of the human immune system to develop transformative therapies for cancer and autoimmune disease. Using its proprietary DECODETM platform—which maps the immune synapse between T cell receptors (TCRs) and their antigen targets—Repertoire translates unique biological insights into potent, targeted immune medicines. The company integrates deep protein engineering expertise and has established collaborations with several leading pharmaceutical companies, including Bristol Myers Squibb, Genentech, Eli Lilly, and Pfizer.
Repertoire is advancing a pipeline of TCR bispecific immunotherapies with the potential to address a broad range of cancers and autoimmune disorders. The company’s lead oncology program, RPTR-1-201, a TCR bispecific, is currently in a Phase 1/2 clinical trial across multiple solid tumor indications. Repertoire plans to advance additional TCR bispecific therapies into clinical trials over the next 12–18 months. The Clinical Trial Associate will play a central role in supporting these programs.Position SummaryRepertoire Immune Medicines is seeking a highly motivated Clinical Trial Associate (CTA) to join our Clinical Operations team and support the execution of early-phase oncology clinical trials. The CTA will provide critical operational support in execution of clinical trials across trial start-up, conduct, maintenance, and close-out activities. In this role, the CTA will work closely with the Director of Clinical Operations and the Clinical Trial Manager, cross-functional team members, CROs, vendors, and clinical sites to help ensure timely, high-quality operational execution of clinical trial activities in compliance with ICH-GCP, applicable FDA and global regulatory requirements, GDPR/HIPAA where relevant, and Repertoire SOPs.
The ideal candidate is detail-oriented, highly organized, proactive, and comfortable working in a fast-paced biotech sponsor environment, with experience supporting oncology and early-phase clinical trials preferred.
The successful candidate will also value a highly collaborative, in-person team culture and be expected to work on-site in our Cambridge office three or more days per week.Key Responsibilities
Clinical Trial Execution and Operational Support
  • Support operational full life cycle execution of early-phase oncology clinical trials in accordance with protocol requirements, ICH-GCP, applicable global regulations, and company SOPs.
  • Coordinate trial activities across multiple functional areas, CROs, vendors, and clinical sites to support timely execution of trial deliverables and milestones.
  • Identify operational issues, assess potential impact to trial timelines or compliance, and escalate risks or mitigation recommendations to Clinical Operations leadership as appropriate.
  • Support site activation, readiness for investigational product release, trial supply coordination, and issue resolution activities.
  • Maintain trial trackers, distribution lists, reports, and clinical systems.
  • Track trial progress, including key milestones, vendor deliverables, enrollment, monitoring activities, and trial action items.
Regulatory, Trial Master File (TMF), and Compliance Support
  • Manage, organize, and maintain trial documentation to support inspection readiness and perform TMF quality checks including identification and resolution of documentation gaps, inconsistencies, and compliance risks.
  • Support preparation, review, tracking, and maintenance of regulatory and IRB/IEC documentation in collaboration with internal and external stakeholders.
  • Support audit and inspection readiness activities, including document retrieval, issue tracking, and follow-up coordination.
  • Track protocol deviations, operational issues, and compliance concerns, including escalation of significant risks to trial leadership.
Cross-Functional Coordination and Trial Oversight
  • Serve as an operational contact for CROs, vendors, and clinical sites under the direction of Clinical Trial Manager.
  • Coordinate trial meetings, prepare agendas and minutes, document key decisions and action items, and support timely follow-up and resolution of operational priorities.
  • Support operational oversight of CRO and vendor deliverables, timelines, and issue escalation activities.
  • Coordinate exchange of trial information and materials across cross-functional stakeholders to support execution and inspection readiness.
  • Exercise independent judgment in prioritizing competing operational activities and managing multiple trial deliverables.
Qualifications
  • Bachelor’s degree in life sciences, health sciences, nursing, public health, or related field.
  • Minimum of 2 years of experience supporting clinical operations, clinical research, or clinical trial execution activities.
  • Working knowledge of ICH-GCP, FDA regulations, and clinical trial processes within a biotech, sponsor, CRO, or research environment.
  • Experience with clinical systems and tools such as eTMF, EDC, CTMS, Smartsheet, Box, and Microsoft Office applications.
  • Strong organizational, analytical, and problem-solving skills with demonstrated ability to prioritize competing activities and manage multiple deliverables.
  • Ability to identify operational risks, support issue resolution, and escalate quality or compliance concerns appropriately.
  • Strong communication and cross-functional collaboration skills with internal and external stakeholders.
  • Experience supporting oncology or early-phase clinical trials is preferred.
The base salary for this role ranges from $62,000 to $86,000 and is determined based on a candidate’s skills, experience, and internal equity. In addition to a competitive base salary, Repertoire offers a broad range of benefits designed to attract, retain, and motivate top talent, including medical, dental, vision, and life insurance, flexible time off, a 401(k) retirement plan, and short- and long-term incentive opportunities. Compensation and benefits are based on Repertoire’s good faith estimate at the time of publication and may be updated in the future.
 
Repertoire is committed to building an inclusive culture.  Much as the power of the immune system lies in the diversity of T and B cells, we believe our best work comes from a diverse workforce—and we are committed to pursuing that in all facets of the work experience.
Repertoire is proud to be an Equal Opportunity Employer.  

Recruitment & Staffing Agencies: Repertoire Immune Medicines (“Repertoire”) does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Repertoire or its employees is strictly prohibited unless contacted directly by Repertoire’s internal Human Resources team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Repertoire, and Repertoire will not owe any referral or other fees with respect thereto.

Powered by JazzHR

o2iNhCDhfn