ZipRecruiter

Log In

1

Research Site Director Jobs (NOW HIRING)

Alcanza

Clinical Research Site Director

Maitland, FL · On-site

The Clinical Site Director is responsible for driving operational performance for of the research site. Provides on-site oversight to help ensure execution and coordination of clinical research ...

Alcanza

Clinical Research Site Director

Orlando, FL · On-site

The Clinical Site Director is responsible for driving operational performance for of the research site. Provides on-site oversight to help ensure execution and coordination of clinical research ...

SQRL

Clinical Research Site Director

Miami, FL · On-site

Direct specialty recruiting strategy * Work closely with the Quality and Risk teams, team leads/site managers and department managers to establish and maintain SOPs and policies and procedures to ...

Evolution Research Group

Site Director

Miami, FL · On-site

$175K - $200K/yr

S. based, privately held, independent clinical research site company, and provider of clinical ... The Site Director is responsible for the profitable management of the clinical research business ...

Green Key Resources

Site Director

Orlando, FL · On-site

The Clinical Site Director is responsible for driving operational performance for of the research site. Provides on-site oversight to help ensure execution and coordination of clinical research ...

next page

Showing results 1-20

All JobsScience JobsResearch JobsResearch Site Director Jobs

Research Site Director information

See salary details

$57.5K

$191.3K

$230.5K

How much do research site director jobs pay per year?

As of Sep 3, 2026, the average yearly pay for research site director in the United States is $191,320.00, according to ZipRecruiter salary data. Most workers in this role earn between $135,500.00 and $229,000.00 per year, depending on experience, location, and employer.

What is a research site director?

Research Site Directors are professionals responsible for overseeing the operations and management of research facilities or sites, typically in clinical trials or scientific studies. They ensure that research protocols are followed, supervise staff, manage budgets, and maintain compliance with regulations and ethical guidelines. Their role is crucial in ensuring the integrity and success of research projects by coordinating logistics, maintaining quality standards, and serving as the primary point of contact between the research site and sponsors or regulatory bodies.

What are the key skills and qualifications needed to thrive as a research site director?

To thrive as a Research Site Director, you need strong leadership abilities, project management experience, and a background in clinical research, typically supported by an advanced degree in a scientific or healthcare field. Familiarity with regulatory compliance systems, electronic data capture (EDC) tools, and certifications like GCP (Good Clinical Practice) are essential. Excellent communication, problem-solving skills, and the ability to build effective teams set standout directors apart. These skills ensure regulatory adherence, efficient study execution, and high-quality research outcomes at the site level.

What are some common challenges a research site director may face in managing multiple clinical trials simultaneously?

A Research Site Director often juggles several clinical trials at once, which can present challenges such as coordinating cross-functional teams, ensuring regulatory compliance, and managing competing timelines. Balancing the needs of different sponsors while maintaining high-quality data and patient safety standards requires strong organizational skills and adaptability. Clear communication with investigators, study coordinators, and sponsors is essential to resolve issues quickly and keep all studies on track.

What is the difference between Research Site Director vs Research Coordinator?

AspectResearch Site DirectorResearch Coordinator
CredentialsBachelor's or higher in related field, often with management experienceBachelor's degree, often in health or science fields
Work EnvironmentOversees entire research site, manages staff, budgets, and complianceAssists with daily research activities, data collection, and participant coordination
Employer & Industry UsageUsed in clinical research, academic, and industry settingsCommon in clinical trials and research institutions
Search & Comparison IntentUnderstanding leadership roles in research sitesFocus on research support and coordination tasks

The Research Site Director typically holds a leadership role overseeing the entire research site, managing staff, budgets, and compliance. In contrast, the Research Coordinator focuses on supporting research activities, data collection, and participant management. Both roles are essential in clinical research but differ in scope, responsibilities, and level of oversight.

What cities are hiring for Research Site Director jobs?

Cities with the most Research Site Director job openings:

What states have the most Research Site Director jobs?

States with the most job openings for Research Site Director jobs include:

Infographic showing various Research Site Director job openings in the United States as of August 2026, with employment types broken down into 97% Full Time, and 3% Part Time. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $191,320 per year, or $92 per hour.

Clinical Research Site Director

DM Clinical Research

Oakland, CA

Full-time

Re-posted yesterday

Job description

Clinical Research Site Director

DM Clinical Research, the largest privately-owned research management organization in the Houston area and one of the top 50 CROs in the country, is looking for an experienced Clinical Research Site Director to join our team of professionals. This role will be responsible for managing clinical trials from startup to closeout by coordinating site operations.
Responsibilities and Duties:
  • Completing all the DMCR-required training, including but not limited to ICH-GCP Certification and IATA Certification on a timely basis.
  • Maintaining a working knowledge of current FDA regulations, ICH-GCP guidelines, all the organizational SOPs, all the guidance documents and assigned study protocol(s).
  • Responsible for immediate supervision and performance of the assigned site staff.
  • Completing all the relevant training prior to study-start and on a continued basis in a timely manner. This will include, but is not limited to:
    • Sponsor provided and IRB approved Protocol Training
    • All relevant Protocol Amendments Training
    • Any study specific Manuals Training as applicable
    • Sponsor-specified EDC and/or IVRS and any other relevant Electronic Systems training.
It is the responsibility of the Site Director to make sure all the relevant training is completed prior to performing any applicable tasks on the assigned study.
  • Working knowledge of the recruitment and relevant cross functional departmental processes for their assigned protocol(s) at their respective site(s).
  • Ensuring visit preparedness for all the relevant sponsor and CRO visits for their assigned protocol(s) and appropriate as well as timely follow up on the action items, at their respective sites.
  • Making sure that the most recent versions of the Protocol, Informed Consents, Study Manuals and all the other relevant study related documents are utilized and implemented at all times for the assigned protocol(s) at their respective site(s).
  • Working with the Regulatory Team to ensure maintenance of Essential Clinical Trial Documents and maintenance of the Investigator Site Binders for their as for their assigned protocol(s) at their respective site(s)
  • Working with the cross functional team(s) and site team(s) to ensure study start readiness on all the aspects and adequate training completed by all the relevant site staff prior to FPFV.
  • Ensuring clinical trial management from FPFV to study close out with strict adherence to study protocol, adherence to all other relevant study manuals, study documents, ICH-GCP Guidelines, FDA Regulations, and ALCOA-C standards, organizational SOPs and guidance documents.
  • Responsible for providing guidance to the site team on planning and monitoring the conduct of the clinical trials.
  • Accomplishing site objectives by managing staff; facilitating staff training as applicable; communicating job expectations
  • Coaching, counseling and disciplining the employees as applicable.
  • Collaborating with both internal and external cross-functional stakeholders for the successful conduct and management of assigned protocol(s) at their respective sites.
  • To develop, coordinate, and enforce site specific systems, policies, procedures, and productivity standards.
  • Communicating and effective implementation of strategic goals from senior management
  • Striving to meet Sponsor subject enrollment goals for their assigned protocols at their respective site(s).
  • Striving to ensure weekly, monthly and quarterly assigned goals are met for their respective site(s).
  • Being prepared for and available at all required company meetings.
  • Submitting required administrative paperwork per company timelines.
  • Occasionally attending out-of-town Investigator Meetings.
  • Any other matters as assigned by management.
Experience and Skill Requirements:
  • Minimum of 8-years experience in Clinical Research.
  • 5 years Experience Managing Multiple Clinical Trials
  • Experience Managing Teams

Apply