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Clinical Trial Jobs (NOW HIRING)

Candel Therapeutics

Clinical Trial Associate

Needham, MA · On-site

$88K - $100K/yr

The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials. This role includes working on multiple protocols with the potential to cross-train across different ...

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead study-specific meetings (e.g., internal core team meetings, investigator meetings, etc), as needed

Frontier Medicines

Clinical Trial Manager

Boston, MA · Hybrid

$120K - $150K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Frontier Medicines is seeking two Clinical Trial Managers to support the day-to-day execution of our oncology clinical trials as they advance through clinical development. Working under the guidance ...

OCUGEN OPCO INC

Clinical Trial Manager

Malvern, PA · On-site

Position Summary The Clinical Trial Manager (CTM) is responsible for the overall operational management and execution of clinical trials from initiation through close-out. This includes leading the ...

Ardelyx

Clinical Trial Associate

Newark, CA

$86K - $105K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

The Clinical Trial Associate (CTA) supports the Clinical Trial Management team in the execution of assigned clinical trials, ensuring operational excellence, compliance with ICH-GCP and applicable ...

Ocugen Inc

Clinical Trial Manager

Malvern, PA · On-site

Position Summary The Clinical Trial Manager (CTM) is responsible for the overall operational management and execution of clinical trials from initiation through close-out. This includes leading the ...

Frontier Medicines

Clinical Trial Manager

Boston, MA · On-site

$120K - $150K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Frontier Medicines is seeking two Clinical Trial Managers to support the day-to-day execution of our oncology clinical trials as they advance through clinical development. Working under the guidance ...

Icon plc

Clinical Trial Assistant

San Francisco, CA · Hybrid

$56K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

New

Icon plc

Clinical Trial Assistant

San Francisco, CA · Hybrid

$56K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

New

Sagimet Biosciences

Clinical Trial Manager

San Mateo, CA · On-site

$90 - $100/hr

Job Type Contract Description The Clinical Trial Manager manages and leads the day-to-day clinical trial activities related to the development and execution of cross-functional and third-party vendor ...

Summit Therapeutics

Clinical Trial Associate

Palo Alto, CA · On-site

$39.50 - $53.75/hr

SENIOR CLINICAL TRIAL ASSOCIATE Overview of Role: The Senior Clinical Trial Associate (Senior CTA) is an experienced clinical operations professional who is responsible for supporting the daily ...

New

ICON

Clinical Trial Assistant

San Francisco, CA · On-site

$56K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Trial Assistant (San Francisco, CA) ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Sitelabs

Clinical Trial Coordinator

Miami, FL · On-site

$55K - $70K/yr

  • Retirement

  • PTO

Role Overview The Clinical Trial Coordinator is responsible for implementing and supporting multiple clinical trial programs across SiteLabs' decentralized pharmacy network. You will act as the ...

Verastem

Clinical Trial Manager

Boston, MA · On-site

$100K - $125K/yr

We are seeking a Clinical Trial Manager with experience in managing a global Phase 3 clinical trial. Works with senior Clinical Operations members to lead the clinical project team members in the ...

TransMedics

Clinical Trial Manager

Andover, MA · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

POSITION SUMMARY This Clinical Trial Manager role is responsible for leading the end-to-end execution of clinical trials, ensuring studies are delivered on time, within budget, and in compliance with ...

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Clinical Trial information

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How much do clinical trial jobs pay per hour?

As of Aug 15, 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 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?

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 jobs are there in clinical trials?

Jobs in clinical trials include clinical research coordinators, clinical research associates, data managers, regulatory affairs specialists, and study nurses. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically a research site, hospital, or pharmaceutical company, with schedules varying from standard to flexible hours depending on the role.

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 to get into a clinical trial career?

A career in clinical trials typically requires a background in healthcare, life sciences, or related fields, along with knowledge of Good Clinical Practice (GCP) guidelines. Entry-level roles often require a bachelor's degree, and certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects. Gaining experience through internships or entry-level positions in research settings is also beneficial.
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Clinical Trial jobs near you
Infographic showing various Clinical Trial job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Associate

Candel Therapeutics

Needham, MA • On-site

$88K - $100K/yr

Full-time

Re-posted yesterday

Job description

  • Location:Hybrid, Needham, MA
  • Salary: $88k-$100k

Why Work With Us?
At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. Like a team, we show up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day.
Our Science: Advancing Cancer Immunotherapies
Candel is a clinical-stage biopharma company developing off-the-shelf, multimodal immunotherapies that stimulate personalized, systemic anti-tumor responses. Our platforms use genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, it's an exciting time to join us and help bring transformative cancer treatments to patients. Learn more:www.candeltx.com
Position Summary:
The Clinical Trial Associate (CTA) role supports clinical trial execution in Ph 2 and Ph 3 trials. This role includes working on multiple protocols with the potential to cross-train across different oncology indications using a variety of clinical trial databases.
Essential Areas of Responsibility:
  • Execute and support day-to-day clinical trial operations in alignment with protocols, timelines, and regulatory requirements.
  • Participate in reviewing, formatting, and finalizing study-related templates, logs, plans, and manuals and ongoing training of personnel.
  • Assist in collecting and completing essential study-related activities, including data entry into multiple databases.
  • Ensure the quality of data submitted from assigned study tasks and timely data submission, including appropriate progress reporting.
  • Manage imaging vendor and maintain tracking of invoices, sample delivery and recovery from the vendor site.
  • Assist in the planning and organizing study-specific meetings and write and distribute regular updates.
  • Assist the Clinical Trial Manager in select site management activities. This could include a review of monitoring reports and source document review.
  • Maintain study-related trackers that will support Clinical Operations and individual studies.
  • Perform primary review of submitted clinical data, database entry, and source document verification according to established standard operating procedures (SOPs).
  • participate in the review and verification of data for quality control processes.
  • Ensure quality in documentation and archiving of clinical data.
  • Support invoice tracking, purchase order coordination, and budget-related activities for study.

Minimum Education, Experience and Skill Requirements:
Education:
  • Bachelor's degree in a health-related discipline or similar.

Experience:
  • At least 2 years of experience in the clinical research/pharmaceutical/biotech arena and an understanding of clinical research and the requirements of a clinical operations function.
  • Excellent verbal and written communication skills, good organizational and interpersonal skills, and team drive.
  • Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with industry best practices.
  • Able to manage multiple projects independently and use varying databases and management systems.
  • Discretion in handling confidential information.
  • Knowledge of project management tools and practices and proficiency in using normal office software: Microsoft Word, Excel, and PowerPoint.

Must be authorized to work in US. We cannot provide sponsorships.
*** NOTE: We are not accepting resumes from agencies. ***

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