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Part Time Clinical Research Director information

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How much do part time clinical research director jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for part time 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 is the difference between Part Time Clinical Research Director vs Clinical Research Coordinator?

AspectPart Time Clinical Research DirectorClinical Research Coordinator
CredentialsAdvanced degrees (e.g., MS, PhD), industry experienceBachelor's degree, relevant certifications
Work EnvironmentOversees multiple studies, strategic planningManages daily study activities, data collection
Employer & Industry UsagePharmaceutical companies, research institutionsHospitals, clinics, research sites

The Part Time Clinical Research Director focuses on overseeing research programs and strategic decisions, often working part-time, while the Clinical Research Coordinator handles daily study operations and participant management. Both roles require relevant industry experience but differ in scope and responsibilities.

What cities are hiring for Part Time Clinical Research Director jobs? Cities with the most Part Time Clinical Research Director job openings:
What are the most commonly searched types of Part Time Clinical Research jobs? The most popular types of Part Time Clinical Research jobs are:
What states have the most Part Time Clinical Research Director jobs? States with the most job openings for Part Time Clinical Research Director jobs include:
Part Time Clinical Research Director jobs near you

Clinical Research Assistant (Must Live in Los Angeles and Speak Spanish)

Angel City VA

Los Angeles, CA • On-site

Part-time

Re-posted 22 days ago

Job description

Title: Part time Clinical Research assistant
Job Summary:
The Research Assistant I provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Essential Responsibilities and Duties:
• Creating and maintaining patient charts for all assigned studies.
• Preparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Filing of lab results, EKG results, and other communication in designated patient charts.
• Maintaining inventory of study specific supplies including lab kits, assessments and participant facing materials.
• Timely completion of data entry and query resolution for all CRFs, based on sponsor specific timelines and deadlines established in contract or other communication.
• Assisting Coordinators in assessments, blood pressure, urine collection, draw labs
• Communicating with study participants, caregivers, third party vendors and laboratories as needed.
• Assisting Coordinators with scheduling, copying, faxing, and other clerical tasks.
• Aiding Coordinators in the facilitation of study monitoring visits.
• Completion of daily responsibilities delegated by CRC as they pertain to the study and/or participants.
• Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
• Office/administrative tasks assigned ie: resupplying exam rooms, ordering office supplies, answering phone calls, etc.
Education/Experience/Skills:
• High school graduate or equivalent. Bac
• Excellent computer skills and advanced knowledge of electronic equipment (i.e., e-mail, computer, fax machine, copier, etc.).
• Skilled in organization and record maintenance.
• Strong personal initiative and attention to detail.
• Ability to clearly communicate both orally and verbally.
• Prior experience in healthcare, research, or clinical settings is a plus.
• Basic knowledge of clinical research processes and regulations (GCP, FDA, IRB) is a plus.

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