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Clinical Trials Director Jobs (NOW HIRING)

Clinical Trials Monitor

Chicago, IL ยท On-site

  • Medical

  • Retirement

  • PTO

... direct costs in peer-reviewed cancer research grants, and $24 million in non-peer-reviewed grants ... The UCCCC has one of the largest cancer clinical trials programs in the country and in the Chicago ...

... the new clinical trials, accrual performance for all trials within the portfolio, escalating ... The Manager will work in collaboration with the Research Division Medical Director, HRI Directors ...

... the new clinical trials, accrual performance for all trials within the portfolio, escalating ... The Manager will work in collaboration with the Research Division Medical Director, HRI Directors ...

$77K - $116K/yr

The Manager, Clinical Trials Projects, leads and oversees the Project Management Team for the URCC ... Reporting to the Executive Director of Research Operations, this role supervises the Project ...

Clinical Trials & Strategy Medical Director

Waltham, MA ยท On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

With supervision, oversees the direction, planning, execution and interpretation of clinical trials ... Qualifications Medical Director Qualifications * Medical Doctor (M.D.), Doctor of Osteopathy (D.O ...

Under the direction of the Director of the Office of Research, the manager oversees all aspects of the department as they relate to management of Oncology and non-Oncology Clinical Trials. The ...

Clinical Trials Manager-B

Stamford, CT ยท On-site

  • Medical

  • Retirement

  • PTO

Under the direction of the Director of the Office of Research, the manager oversees all aspects of the department as they relate to management of Oncology and non-Oncology Clinical Trials. The ...

Under the direction of the Director of the Office of Research, the manager oversees all aspects of the department as they relate to management of Oncology and non-Oncology Clinical Trials. The ...

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Clinical Trials Director information

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$10

$54

$116

How much do clinical trials director jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for clinical trials director in the United States is $54.33, according to ZipRecruiter salary data. Most workers in this role earn between $32.45 and $71.63 per hour, depending on experience, location, and employer.

What is the difference between Clinical Trials Director vs Clinical Research Manager?

AspectClinical Trials DirectorClinical Research Manager
ResponsibilitiesOversees entire clinical trial programs, manages teams, and ensures regulatory complianceManages daily operations of clinical research projects, coordinates activities, and supports trial execution
Required CredentialsTypically requires a clinical research or life sciences degree, with extensive experienceRequires similar degrees and experience, often with less strategic oversight
Work EnvironmentSenior leadership in pharmaceutical or biotech companies, overseeing multiple projectsOperational roles within research sites or CROs, focusing on project execution

The Clinical Trials Director focuses on strategic oversight and leadership of clinical trial programs, while the Clinical Research Manager handles day-to-day project management. Both roles require relevant credentials and industry experience, but differ in scope and level of responsibility.

What are some common challenges faced by a clinical trials director and how can they be managed?

Clinical Trials Directors often encounter challenges such as coordinating large, cross-functional teams, ensuring strict regulatory compliance, and managing tight timelines for multiple studies. Effective communication, strong leadership, and proactive risk management are essential to address these issues. Staying updated on regulatory changes and fostering collaboration between departments can also help streamline processes and ensure trials run efficiently.

What does a clinical trials director do?

A Clinical Trials Director oversees the planning, execution, and management of clinical research trials to ensure they are conducted ethically, safely, and in compliance with regulatory standards. They coordinate with cross-functional teams, manage budgets and timelines, and ensure that trials meet scientific and operational objectives. Their responsibilities also include liaising with regulatory agencies, monitoring trial progress, and addressing any issues that arise during the study.

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

To thrive as a Clinical Trials Director, you need a strong background in clinical research, regulatory compliance, and project management, typically supported by an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and certifications like ACRP or SOCRA are commonly required. Exceptional leadership, strategic thinking, and communication skills are crucial for managing cross-functional teams and stakeholder relationships. These competencies ensure successful trial execution, regulatory adherence, and the delivery of safe and effective clinical outcomes.
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What cities are hiring for Clinical Trials Director jobs?

Cities with the most Clinical Trials Director job openings:

What are the most commonly searched types of Clinical Trials jobs?

The most popular types of Clinical Trials jobs are:

What states have the most Clinical Trials Director jobs?

States with the most job openings for Clinical Trials Director jobs include:

Infographic showing various Clinical Trials Director 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 $113,010 per year, or $54.3 per hour.

Assistant Director for Clinical Trials

Stony Brook University Medical

Stony Brook, NY โ€ข On-site

Full-time

Posted 24 days ago


Job description

Required Qualifications (as evidenced by an attached resume):
Bachelor's degree (foreign equivalent or higher) plus three (3) years of full-time experience in clinical research with two (2) years of this working with sponsored clinical trials. Administrative and managerial experience working with research projects and clinical trials involving an external sponsor. Supervisory experience to include supervising research coordinators. Experience working with research protocols and budget preparation and negotiation with the sponsor.
Preferred Qualifications:ย 
Master's degree (foreign equivalent or higher). Four (4) or more years of full-time experience in clinical research involving sponsored clinical trials. Proficient in ONCOR Clinical Trials Management System. Bilingual in Spanish.
Brief Description of Duties:
The incumbent directs the day-to-day operations of the Clinical Research Core, developing, managing, and evaluating all administrative and financial policies and procedures of the office. Responsible for developing position descriptions, hiring, training, supervising, performing yearly reviews, etc. Provides expertise, training, and mentoring to research staff, not limited to Investigators and Study Coordinators. Facilitates study start up (budget development, contract negotiation, administrative approvals, etc.), as well as manages financial aspects of industry funded clinical trials for a number of departments within the SOM. Establishes collaborative processes and shared resources among other SUNY campuses with the goal of identifying common needs. Reports directly to the Associate Director for Clinical Trials at Stony Brook School of Medicine.
ย 

Duties:

Staff/Personnel Responsibilities:

ย ย ย ย ย ย ย ย  Supervises CRC staff, providing specific work assignments to staff in order to facilitate research at SBU, performing QA on assigned work, carrying out performance programs reviews and evaluations, managing time off requests, etc.

ย ย ย ย ย ย ย ย  Ensure that policies and procedures are adhered to.

ย ย ย ย ย ย ย ย  Trains and mentors' staff (PI's, department administrators, Study Coordinators, etc.) on research-related practices.

ย ย ย ย ย ย ย ย  Facilitates educational research training to study coordinators throughout the year.

Financial Responsibilities:

ย ย ย ย ย ย ย ย  Budget development and negotiation for industry-funded clinical trials for SOM.

ย ย ย ย ย ย ย ย  Payment Terms negotiation with sponsors.

ย ย ย ย ย ย ย ย  Management of Clinical Conductor Clinical Trails Management System (CTMS). Creation of new studies and their negotiated budget

ย ย ย ย ย ย ย ย  Training of Study Coordinators on the use of the CTMS.

ย ย ย ย ย ย ย ย  Provide technical support to users of CTMS.

ย ย ย ย ย ย ย ย  Run monthly financial reports and queries for data entry.

ย ย ย ย ย ย ย ย  Study invoicing, payments, accounts reconciliation, and closeout.

Other:

ย ย ย ย ย ย ย ย  Oversees regulatory aspects of studies, such as IRB submission and ClinicalTrials.gov entries for research compliance.

ย ย ย ย ย ย ย ย  Day-to-Day study coordination, including patient recruitment and consent, study visits, collection, preparation, shipping of human samples, and data entry.

ย ย ย ย ย ย ย ย ย  Preparation of necessary documents, figures, and tables for research presentations, Data and Safety Monitoring Board meetings, and sponsor audits.

Other Duties as assigned


Special Notes:
The Research Foundation of SUNY is a private educational corporation. Employment is subject to the Research Foundation policies and procedures, sponsor guidelines and the availability of funding. FLSA Exempt position, not eligible for the overtime provisions of the FLSA. Minimum salary threshold must be met to maintain FLSA exemption.

Essential Position: This has been designated as an essential position based on the duties of the job and the functions performed. Positions that are designated as such may be required to report to work/remain at work even if classes are canceled, and the campus is working on limited operations in an emergency.

For this position, we are unable to sponsor candidates for work visas.
Resume/CV and cover letter should be included with the online application.
Stony Brook University is committed to excellence in diversity and the creation of an inclusive learning, and working environment. All qualified applicants will receive consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, familial status, sexual orientation, gender identity or expression, age, disability, genetic information, veteran status and all other protected classes under federal or state laws.
If you need a disability-related accommodation, please call the university Office of Equity and Access (OEA) at (631) 632-6280 or visit OEA.
In accordance with the Title II Crime Awareness and Security Act a copy of our crime statistics can be viewed here.
Visit our WHY WORK HERE page to learn about the total rewards we offer.
SUNY Research Foundation: A Great Place to Work.
The starting salary range (or hiring range) to be offered for this position is noted below, it represents SBU's good faith and reasonable estimate of the range of possible compensation at the time of posting.

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