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Evening Clinical Research Instructor Jobs (NOW HIRING)

San Antonio, TX The Clinical Research Nurse/Registered Nurse II will be responsible for the Nursing ... May require occasional weekend and evening hours * Other duties as assigned Qualifications

San Antonio, TX The Clinical Research Nurse/Registered Nurse II will be responsible for the Nursing ... May require occasional weekend and evening hours * Other duties as assigned Qualifications

BLS - Basic Life Support or Instructor (AHA) - American Heart Association SKILLS AND ABILITIES ... Precepts new clinical research staff in clinical setting. Uses peer-to-peer accountability towards ...

In this role you should plan to work some evening and weekends. Primary Responsibilities: You are ... Clinical Research experience useful, but not required If you are a Gmail user and you chose to ...

Clinical Research Coordinator

Lincoln, NE · On-site

$21 - $28/hr

In this role you should plan to work some evening and weekends. Primary Responsibilities: You are ... Clinical Research experience useful, but not required If you are a Gmail user and you chose to ...

Clinical Research Coordinator

Lincoln, NE · On-site

$21 - $28/hr

In this role you should plan to work some evening and weekends. Primary Responsibilities: You are ... Clinical Research experience useful, but not required If you are a Gmail user and you chose to ...

Clinical Research Coordinator

Palo Alto, CA · On-site

$35 - $70/hr

  • Medical

  • Dental

  • Vision

Clinical Research Coordinator Pay Rate Range: $35.00 - $70.00/hr (DOE, based on experience and ... Occasional evening or weekend hours may be required for study visits or participant needs. * Must ...

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Evening Clinical Research Instructor information

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$31K

$68.7K

$115.5K

How much do evening clinical research instructor jobs pay per year?

As of Aug 15, 2026, the average yearly pay for evening clinical research instructor in the United States is $68,661.00, according to ZipRecruiter salary data. Most workers in this role earn between $49,500.00 and $83,500.00 per year, depending on experience, location, and employer.

What is the difference between Evening Clinical Research Instructor vs Clinical Research Coordinator?

AspectEvening Clinical Research InstructorClinical Research Coordinator
CredentialsTypically requires a degree in health sciences or related field, plus teaching experienceRequires a bachelor's degree, often in health sciences, with certification preferred
Work EnvironmentEducational settings, classrooms, training programs, eveningsClinical sites, hospitals, research facilities, often full-time during regular hours
Employer & IndustryEducational institutions, training organizationsResearch institutions, hospitals, pharmaceutical companies
Primary FocusTeaching clinical research principles and protocols in evening classesManaging and coordinating clinical trials at research sites

The Evening Clinical Research Instructor primarily focuses on teaching and training students in clinical research during evening hours, often within educational settings. In contrast, the Clinical Research Coordinator manages and oversees clinical trials at research sites during regular working hours. Both roles require knowledge of clinical research, but their work environments and responsibilities differ significantly.

What cities are hiring for Evening Clinical Research Instructor jobs?

Cities with the most Evening Clinical Research Instructor job openings:

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 Evening Clinical Research Instructor jobs?

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

Full-time

Posted 15 days ago


Job description

Summary

CHENEGA RELIABLE SERVICES, LLC.

San Antonio, TX

The Clinical Research Nurse/Registered Nurse II will be responsible for the Nursing Department service areas including Trauma, Critical Care, Oncology, Neuroscience, Behavioral Health, Pediatrics, Medical Surgical Specialties, Perioperative Nursing, Interventional Radiology, Diabetes care, Inpatient care services, outpatient clinic and more.


Responsibilities
  • Manages all areas of clinical studies, including protocol development, regulatory submissions, and data management, specifically preparing protocol submissions, informed consent forms, annual reports, and study amendments for appropriate IRBs of record
  • Provides documentation submissions in accordance with federal and local regulations.
  • Manages patients on clinical studies/trials per research protocol, collects and reports adverse events, participates in weekly team meetings, and works with study team to open new clinical studies/trials
  • Educates staff and patients on assigned study protocols/clinical trials.
  • Maintains all clinical research documentation to support ongoing and future studies in support of the principal investigator and the project staff.
  • Responsible for patient evaluations, communications to pharmaceutical sponsors regarding status of enrolled patients, and study data collection results to investigator as applicable (critical lab results, etc.).
  • Instructs and counsels patients in research procedures, to include administration, monitoring, recording and analyzing data.
  • Provides general supervision related to the conduct of all research protocols and reports back to the Principal Investigator(s).
  • Ensures compliance with all federal and local regulations.
  • Supports government executive director(s) in the planning, evaluation, implementation, and documentation of scientific research utilizing specimens for clinical projects.
  • Coordinates clinical experiment scheduling and collection of data; work with clinical research coordinators; recruits and enrolls clinical study participants; provides ethical oversight in support of the clinical study.
  • May be required to collect study samples from patients to support the clinical research effort.
  • Documents results of study participants in accordance with protocols; schedules and coordinates research resources; gathers, compiles, organizes, analyzes and reports research information and study results.
  • Sets up and assigns protocol procedures and preclinical (bench or animal) experiments; monitors budget plans and management
  • Researches and prepares equipment and supplies in accordance with institutional procedures.
  • May require occasional weekend and evening hours
  • Other duties as assigned

Qualifications
  • Associate degree in Nursing (ADN)
  • Possess and maintain an active and unencumbered Registered Nursing (RN) License issued by the state of Texas.
  • Minimum five (5) years clinical/acute care experience
  • Minimum three (3) years’ clinical research experience and research design.

Preferred Qualifications

  • Bachelor of Science in Nursing (BSN)
  • Possess and maintain Certified Clinical Research Coordinator (CCRC).

 

Knowledge, Skills and Abilities

  • Experience in a research and clinical setting
  • Experience in either the military, federal, private or public sector, performing the following types of tasks:
    • Providing comprehensive nursing care to patients
    • Administering oxygen, IV fluid, blood transfusions and prescribed oral, subcutaneous and intramuscular medications
    • Managing nasal-pharyngeal and gastric suction as well as a variety of other drainage tubes
    • Preparing patients for surgical and/or diagnostic procedures
    • Setting up, operating and monitoring specialized equipment such as cardiac monitors, respirators, defibrillators, etc.
    • Providing care in a variety of clinical settings, such as Inpatient Patient Care Units (e.g. oncology, pediatric, neurology, behavioral health), ICU, Operating Room, PACU, Donor Services, Infusion Centers and Ambulatory Clinics.
  • Ability to complete CITI training and remain current.

 

Physical Demands:(The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)

  • While performing the duties of this Job, the employee is regularly required to sit and talk or hear. The employee may use repeated motions that include the arms, wrists, hands and/or fingers. The employee is occasionally required to walk, stand, climb, balance, stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision.

Any estimated salary provided by this job board may not align with Chenega's compensation program. Please apply to connect with a recruiter who can provide more details.

Qualifications:
  • Associate degree in Nursing (ADN)
  • Possess and maintain an active and unencumbered Registered Nursing (RN) License issued by the state of Texas.
  • Minimum five (5) years clinical/acute care experience
  • Minimum three (3) years’ clinical research experience and research design.

Preferred Qualifications

  • Bachelor of Science in Nursing (BSN)
  • Possess and maintain Certified Clinical Research Coordinator (CCRC).

 

Knowledge, Skills and Abilities

  • Experience in a research and clinical setting
  • Experience in either the military, federal, private or public sector, performing the following types of tasks:
    • Providing comprehensive nursing care to patients
    • Administering oxygen, IV fluid, blood transfusions and prescribed oral, subcutaneous and intramuscular medications
    • Managing nasal-pharyngeal and gastric suction as well as a variety of other drainage tubes
    • Preparing patients for surgical and/or diagnostic procedures
    • Setting up, operating and monitoring specialized equipment such as cardiac monitors, respirators, defibrillators, etc.
    • Providing care in a variety of clinical settings, such as Inpatient Patient Care Units (e.g. oncology, pediatric, neurology, behavioral health), ICU, Operating Room, PACU, Donor Services, Infusion Centers and Ambulatory Clinics.
  • Ability to complete CITI training and remain current.

 

Physical Demands:(The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)

  • While performing the duties of this Job, the employee is regularly required to sit and talk or hear. The employee may use repeated motions that include the arms, wrists, hands and/or fingers. The employee is occasionally required to walk, stand, climb, balance, stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision.

Any estimated salary provided by this job board may not align with Chenega's compensation program. Please apply to connect with a recruiter who can provide more details.

Education:UNAVAILABLEEmployment Type: FULL_TIME