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Part Time Clinical Research Instructor Jobs (NOW HIRING)

Gavilan College

Part-Time Clinical Instructor

Gilroy, CA · On-site

$74.74 - $100.18/hr

GC Definition PART-TIME INSTRUCTOR (PART-TIME NOT TO EXCEED 67% OF A FULL-TIME LOAD) Part-Time Faculty Salary Schedule Starting Salary Ranges: Lecture: $74.74 - $100.18* Lab: $65.26 - $70.07 *Salary ...

Jefferson College

Clinical Instructor

Hillsboro, MO

$40 - $45/hr

Position Information Position Title Clinical Instructor Department Office of Clinical Coordinator Responsibilities Bi-level Nursing program is seeking part-time Clinical Instructors for the Level I ...

Jefferson College

Clinical Instructor

Hillsboro, MO · On-site

$40 - $45/hr

Position Details Position Information Position Title Clinical Instructor Department Office of Clinical Coordinator Responsibilities Bi-level Nursing program is seeking part-time Clinical Instructors ...

Vermont State University

Clinical Instructor

Randolph, VT · On-site

$62/hr

Vermont State University (VTSU) invites applications for part-time clinical instructors to support clinical, laboratory, and simulation instruction in its prelicensure nursing programs, including the ...

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Part Time Clinical Research Instructor information

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$11K

$123.8K

$190.5K

How much do part time clinical research instructor jobs pay per year?

As of Aug 16, 2026, the average yearly pay for part time clinical research instructor in the United States is $123,840.00, according to ZipRecruiter salary data. Most workers in this role earn between $35,500.00 and $175,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a part time clinical research instructor, and why are they important?

To thrive as a Part Time Clinical Research Instructor, you need a background in clinical research, a relevant advanced degree (such as an MS or PhD), and hands-on experience in research methodologies. Familiarity with learning management systems (LMS), electronic data capture tools, and certifications such as CITI or GCP are typically required. Outstanding communication, mentoring, and organizational skills help instructors effectively convey complex concepts and support diverse learners. These skills and qualifications ensure high-quality instruction, regulatory compliance, and successful student outcomes in clinical research education.

What is a part time clinical research instructor?

A Part Time Clinical Research Instructor is a professional who teaches and guides students or trainees in the principles and practices of clinical research on a part-time basis. They often develop and deliver coursework, mentor students, and provide expertise in research methodologies, regulatory requirements, and ethical considerations. These instructors may work in academic institutions, hospitals, or clinical research organizations, balancing teaching responsibilities with other professional commitments. Their role is crucial in preparing the next generation of clinical researchers.

How does a part time clinical research instructor typically balance teaching responsibilities with research obligations?

Part Time Clinical Research Instructors often divide their time between preparing and delivering instructional content to students and staying current with ongoing research activities. Balancing these responsibilities requires effective time management, as instructors must coordinate class schedules, grade assignments, and mentor students while also contributing to or supervising clinical research projects. Collaboration with full-time faculty and research staff is common, and clear communication helps ensure both teaching and research goals are met. Flexibility and adaptability are key, as clinical schedules and research needs can shift throughout the semester.

What is the difference between Part Time Clinical Research Instructor vs Part Time Clinical Research Coordinator?

AspectPart Time Clinical Research InstructorPart Time Clinical Research Coordinator
CredentialsTypically requires a clinical research background, teaching experience, and relevant certificationsRequires clinical research certifications, experience in study coordination, and knowledge of regulatory requirements
Work EnvironmentEducational settings, training programs, academic institutionsResearch sites, hospitals, clinical trial sites
Employer & IndustryUniversities, training organizations, research institutionsPharmaceutical companies, research organizations, hospitals
Primary FocusTeaching clinical research principles and protocolsManaging and coordinating clinical trial activities

While both roles involve clinical research, the Part Time Clinical Research Instructor focuses on education and training, whereas the Part Time Clinical Research Coordinator handles the operational aspects of clinical trials. They share certifications and industry settings but differ in daily responsibilities and objectives.

What are the most commonly searched types of Clinical Research Instructor jobs?

The most popular types of Clinical Research Instructor jobs are:

What states have the most Part Time Clinical Research Instructor jobs?

States with the most job openings for Part Time Clinical Research Instructor jobs include:

Part Time Clinical Research Instructor jobs near you

Clinical Research Physician - Cardiologist (Part time)

Alcanza Clinical Research

Decatur, GA • On-site

Part-time

Medical, Dental, Vision, Life, Retirement

Re-posted 7 days ago

Job description

Clinical Research Physician - Cardiologist (Part time)
Department: Operations
Employment Type: Part Time
Location: Accel Research Sites - Decatur, GA
Reporting To: Adrienne Hilliard
Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Principal Investigator conducts and coordinates daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes. Working with a local and central team drives clinical oversight and the quality of the assigned studies at the site.
Key Responsibilities
Essential Job Duties:
  • Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes
  • Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance
  • Evaluates and assesses participants to ensure only eligible participants enroll into the trials.
  • Participates and engages in successful delivery and retention of study participants.
  • Interacts positively and collaboratively with sponsors, clients and team members.
  • Practices attention to detail in recording data and participant information, following protocol guidelines and GCPs.
  • Actively involved in protocol training for staff.
  • Participate in Investigator Meetings (IMs), and continuing education activities in order to maintain current knowledge of recruitment affairs and issues.
  • Perform other duties as assigned, requested, or required based on the needs of the participants, protocols and/or company.

Skills, Knowledge and Expertise
Minimum Qualifications: MD or DO degree, an active physician license (in good standing) in the state of practice for this role is required. Board certification is required.
Required Skills:
  • Clinical skills and clinical procedures based in area of specialty.
  • Proficiency with computer applications such as MS Office, electronic health records, and web applications, and the ability to type proficiently (40+ wpm).
  • Must possess strong organizational skills, attention to detail, and math proficiency.
  • Well-developed written and verbal communication skills. Bi-lingual (English / Spanish) proficiency is highly preferred.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, employees, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
  • Ability to be professional, respectful of others, self-motivated, and exemplify a strong work ethic.
  • Must possess a high degree of urgency, self-motivation, integrity and dependability.
  • Ability to work independently to identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.

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