ZipRecruiter

Log In

1

Clinical Research Director Jobs (NOW HIRING)

University of Chicago Library

Job Summary The Clinical Research Nurse works in the Department of Pediatrics under the supervision of the Clinical Research Director, Department of Pediatrics Medical Director, and the Principal ...

Vitalief

Clinical Research Nurse

New Brunswick, NJ · On-site

Under the direction of the Clinical Research Director, support primarily Medical Oncology interventional studies (Phase II-III). Studies are largely drug and biologic trials, with limited device ...

Phsorg

The Director of Clinical Research is the senior executive responsible for the strategic, operational, and regulatory leadership of the Presbyterian Healthcare Services clinical research enterprise.

previous page

Showing results 41-60

All JobsClinical Research JobsClinical Research Director Jobs

Clinical Research Director information

See salary details

$10

$54

$116

How much do clinical research director jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for clinical research 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 are the key skills and qualifications needed to thrive as a clinical research director, and why are they important?

To thrive as a Clinical Research Director, you need advanced knowledge of clinical trial design, regulatory compliance, and data analysis, typically supported by a medical, pharmaceutical, or life sciences degree along with significant experience in clinical research. Expertise in systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and familiarity with GCP, FDA, and ICH guidelines are essential, and certifications like CCRP or CCRA are highly valued. Leadership, strategic thinking, and strong communication skills distinguish top performers by enabling effective team management and stakeholder engagement. These competencies ensure that clinical trials are conducted ethically, efficiently, and in compliance with all regulatory standards, driving successful research outcomes.

What are the responsibilities of a clinical research director?

A Clinical Research Director oversees the planning, coordination, and management of clinical trials and research projects within healthcare or pharmaceutical organizations. They ensure studies comply with regulatory requirements, establish research protocols, manage budgets, and supervise research teams. Additionally, they collaborate with stakeholders, analyze data, and ensure that clinical trials are conducted ethically and efficiently to advance medical knowledge and patient care.

What are some of the main challenges a clinical research director faces when overseeing multiple clinical trials simultaneously?

One of the primary challenges for a Clinical Research Director managing multiple trials is ensuring consistent protocol adherence across diverse study sites while maintaining strict regulatory compliance. Balancing resource allocation, addressing unforeseen issues such as patient recruitment delays, and effectively communicating with cross-functional teams also require strong organizational and leadership skills. Additionally, the director must stay updated on evolving industry standards and regulatory requirements to mitigate risks and ensure the integrity of all ongoing studies.

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

AspectClinical Research DirectorClinical Research Manager
ResponsibilitiesOversees multiple projects, strategic planning, and department leadershipManages daily operations of clinical trials, supervises teams, and ensures compliance
Required CredentialsTypically requires a PhD, MD, or advanced degree, along with extensive experienceUsually requires a bachelor's or master's degree in life sciences, with relevant experience
Work EnvironmentSenior leadership in pharmaceutical or biotech companies, overseeing multiple teamsOperational setting within research sites or CROs, directly managing trial teams
Industry UsageCommonly found in large organizations with multiple projectsFound in both large and small organizations, focusing on trial execution

The Clinical Research Director focuses on strategic oversight and leadership of research programs, while the Clinical Research Manager handles day-to-day trial management. Both roles require relevant experience, but the director's role is more senior and strategic.

What does a clinical research director do?

A clinical research director manages medical or pharmaceutical research projects. In this role, you may oversee a research department at a university or medical facility. Your specific job duties vary, depending on the type of project you work on, but your general responsibilities include overseeing the planning stages of each research project or clinical trial, discussing outcomes and expectations with researchers, making sure that research staff members provide the proper care to participants in the trial or research project, and ensuring that data is documented properly. Clinical research directors also hire and train new staff members and check that the project follows all governmental and industry guidelines.

More about Clinical Research Director jobs
What cities are hiring for Clinical Research Director jobs? Cities with the most Clinical Research Director job openings:
What are the most commonly searched types of Clinical Research jobs? The most popular types of Clinical Research jobs are:
Who are the top companies hiring for Clinical Research Director jobs? The top employers for Clinical Research Director jobs are:
What states have the most Clinical Research Director jobs? States with the most job openings for Clinical Research Director jobs include:
What job categories do people searching Clinical Research Director jobs look for? The top searched job categories for Clinical Research Director jobs are:
Clinical Research Director jobs near you
Infographic showing various Clinical Research Director job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% 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.

Clinical Research Coordinator

American Oncology Management Company

Hot Springs, AR • On-site

$53K - $93K/yr

Other

Posted 19 days ago

Job description

Location:

Genesis Cancer and Blood Institute

Pay Range:

$53,040.00 - $93,267.20 Position Summary

The Clinical Research Coordinator functions as an integral part of the Research Team in clinical trial management at Oncology Consultants. The Clinical Research Coordinator is involved in multiple aspects of the research process under the general supervision of the Clinical Research Manager and the Research Director.

Key Performance Areas

KPA 1 - Study Start-Up, Regulatory & Site Initiation

Responsible for supporting study feasibility, regulatory submissions, and study initiation activities to ensure compliance with protocols, regulatory requirements, and institutional policies.

  • Applies knowledge of study design to evaluate protocol feasibility at the site.

  • Assists Regulatory staff in preparing and submitting documents to Institutional Review Board (IRB).

  • Participates in study site initiation activities.

  • Attends and participates in investigator meetings and clinical trial conferences as directed.

  • Documents protocol deviations and exemptions.

  • Prepares for and participates in FDA inspections.

  • Communicates effectively with IRBs, sponsors, investigators, and research team members.

KPA 2 - Patient Recruitment, Screening & Enrollment

Responsible for patient recruitment, screening, eligibility verification, and enrollment activities in accordance with study protocols.

  • Participates in subject/patient recruitment and evaluation of eligibility.

  • Reviews and verifies required source documents to confirm study eligibility.

  • Reviews inclusion/exclusion criteria with investigator to assure subject eligibility.

  • Conducts interviews to assess subject ability and willingness to complete study procedures.

  • Maintains patient screening and enrollment logs.

  • Reviews protocol requirements, informed consent, and follow-up procedures with potential study subjects.

  • Follows randomization procedures per protocol.

  • Demonstrates commitment to superior customer service and patient-centered communication.

KPA 3 - Clinical Trial Coordination & Patient Care Activities

Responsible for coordinating study visits, performing clinical procedures, and ensuring protocol compliance throughout the research process.

  • Ensures study drugs are dispensed per protocol and maintains drug accountability records.

  • Reviews returned drugs for compliance and documents findings.

  • Provides direct care in study compliance throughout the research experience.

  • Performs peripheral venipuncture per organizational standards.

  • Ensures proper specimen collection, batching, processing, and shipping per protocol.

  • Works collaboratively with site staff to process specimens.

  • Prepares and ships study-required specimens per protocol manual.

  • Obtains test results and reports to the physician investigator.

  • Attends clinic visits with the investigator and assists in following study guidelines.

KPA 4 - Data Management, Documentation & Monitoring Support

Responsible for maintaining accurate study documentation, source documentation, and supporting sponsor monitoring and audit activities.

  • Obtains and reviews original source documents (recordings, scans, test results, procedure reports).

  • Abstracts data from medical records and other documentation to study forms and flow sheets.

  • Completes and maintains study documentation and case report forms.

  • Resolves data queries.

  • Schedules sponsor monitoring visits.

  • Prepares case report forms and source documents for sponsor and audit review.

  • Assists with audit preparation and monitoring visits.

KPA 5 - Research Program Support, Education & Administrative Support

Responsible for supporting research department operations, education, budgeting support, and departmental coordination activities.

  • Participates in educational and training activities and continuing education.

  • Supports and assists management team with department projects.

  • Assists in maintenance of budgetary data for each clinical trial.

  • Assists in planning department coverage for clinic visits, data management, and meetings.

  • Maintains professional communication with internal and external customers.

  • Demonstrates strong verbal and written communication skills.

Position Qualifications

Education

  • Degree in the life sciences or health sciences such as Registered Nurse (R.N.), Doctor in Philosophy (Ph.D.), Medical Doctorate (M.D.), or other related degree.

Minimum Relevant Experience

  • 2 or more years of clinical research experience.

Certifications/Licenses

  • Continuing education participation is expected, and research certification through a recognized national organization (SOCRA, ACRP) is encouraged.

  • NIH protection of Human subjects online course will be required annually.

  • IATA training will be required every 2 years.

Travel: 0 - 25%

#AONA

#LI-ONSITE

Apply