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Clinical Trials Coordinator Jobs (NOW HIRING)

Stamford Health

Clinical Trials Manager-B

Stamford, CT · On-site

The department manager manages staff including clinical trials coordinators, data specialists, finance analysts, regulatory coordinators and research assistants, and any other staff deemed necessary ...

NY SCIENTIFIC CORP

Clinical Trials Recruiter

Brooklyn, NY · On-site +1

$20 - $30/hr

Clinical Trials Recruiter Location: Brooklyn, NY / [On-site and Remote] Compensation: based on ... Collaborate with study coordinators and investigators to ensure smooth enrollment. * Develop and ...

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How much do clinical trials coordinator jobs pay per year?

As of Aug 15, 2026, the average yearly pay for clinical trials coordinator in the United States is $67,542.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,500.00 and $78,500.00 per year, depending on experience, location, and employer.

What are some common challenges faced by clinical trials coordinators, and how can they be effectively managed?

Clinical Trials Coordinators often encounter challenges such as strict regulatory compliance, managing multiple timelines, and coordinating communication among diverse stakeholders. Navigating complex protocols and ensuring accurate documentation are also critical aspects of the role. To effectively manage these challenges, coordinators benefit from strong organizational skills, attention to detail, and proactive communication with the research team, sponsors, and participants. Staying current with regulatory requirements and utilizing project management tools can also help streamline processes and reduce errors.

What is a clinical trials coordinator?

Clinical Trials Coordinators are professionals who manage and oversee the daily operations of clinical research studies. They ensure that studies are conducted according to regulatory guidelines, protocols, and ethical standards. Their responsibilities include recruiting and screening participants, collecting and managing study data, coordinating with investigators and sponsors, and ensuring compliance with protocols. They play a vital role in advancing medical research by facilitating the safe and effective testing of new treatments and therapies.

What are the key skills and qualifications needed to thrive as a clinical trials coordinator?

To thrive as a Clinical Trials Coordinator, you need strong organizational skills, knowledge of clinical research protocols, and a background in life sciences or a related field, often supported by a bachelor's degree. Familiarity with clinical trial management systems (CTMS), regulatory compliance tools, and certifications such as Good Clinical Practice (GCP) are highly valued. Attention to detail, effective communication, and problem-solving abilities help ensure smooth collaboration among stakeholders and adherence to protocols. These skills are essential for ensuring regulatory compliance, data integrity, and the successful execution of clinical trials.
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Clinical Trials Coordinator jobs near you
Infographic showing various Clinical Trials Coordinator 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 $67,542 per year, or $32.5 per hour.

Clinical Trials Coordinator (1272)

LIFESTREAM BEHAVIORAL CENTER

Leesburg, FL • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 25 days ago

Job description

Job Purpose:
- The Clinical Trials Coordinator at LIFESTREAM BEHAVIORAL CENTER will be responsible for managing and overseeing clinical trials within the organization. This role is critical in ensuring that all clinical trials are conducted in accordance with regulatory requirements and organizational standards, while also maintaining the highest level of ethical standards. The coordinator will work closely with research teams, healthcare professionals, and participants to facilitate successful trial outcomes and contribute to the advancement of behavioral health research.
Key Responsibilities:
- Coordinate and manage all aspects of clinical trials, including planning, execution, and completion.
- Ensure compliance with all regulatory and ethical guidelines, including those set by the Institutional Review Board (IRB).
- Develop and maintain trial documentation, including protocols, consent forms, and case report forms.
- Liaise with investigators, sponsors, and regulatory bodies to facilitate communication and ensure trial objectives are met.
- Recruit, screen, and enroll trial participants, ensuring informed consent is obtained and documented.
- Monitor trial progress, including participant follow-up and data collection, to ensure adherence to study protocols.
- Manage trial budgets and resources, ensuring efficient use of funds and materials.
- Provide training and support to research staff and trial participants as needed.
- Prepare and present trial reports and findings to stakeholders and regulatory bodies.
- Stay informed of industry trends and advancements in clinical trial management and behavioral health research.

Required Education:
- Bachelor's degree in Life Sciences, Nursing, Public Health, or a related field.
Required Experience:
- Minimum of 2 years of experience in clinical trial coordination or a similar role.
- Proven track record of managing multiple clinical trials simultaneously.
- Experience working in a behavioral health setting is preferred.
- Familiarity with regulatory requirements and guidelines in clinical research.
Required Skills and Abilities:
- Strong organizational skills with the ability to prioritize tasks effectively.
- Excellent communication skills, both written and verbal, for interaction with clinical teams and study participants.
- Proficient in using clinical trial management software and databases.
- Ability to work independently and collaboratively in a team-oriented environment.
- Strong attention to detail and accuracy in data collection and reporting.
- Knowledge of Good Clinical Practice (GCP) and ethical guidelines in clinical research.
- Problem-solving skills and the ability to handle challenging situations with professionalism.

LifeStream Benefits 

  • Health/Dental/Vision Insurance 

  • Short Term Disability 

  • Pension Plan 

  • 403(b) 

  • PTO  (Over 4 weeks your 1st year!) 

  • Flexible Work Schedules 

  • Tuition Reimbursement Program 

  • Free Telehealth Services  

  • And More! 

Apply