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Clinical research • chula vista ca

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Clinical Research Coordinator 1

Clinical Research Coordinator 1

MPF FederalSan Diego, CA, US
[job_card.full_time]
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Clinical Research Coordinator I.Naval Health Research Center (NHRC).Patient Recruitment and Consent : Identifies,.Help lead recruitment efforts, developing and refining strategies to meet enrollment...[show_more][last_updated.last_updated_30]
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Research Assistant

Research Assistant

TradeJobsWorkForce92163 San Diego, CA, US
[job_card.full_time]
Research Assistant Job Duties : Generates hypotheses and designs and performs experiments to test th...[show_more][last_updated.last_updated_30]
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Assistant Clinical Research Coordinator

Assistant Clinical Research Coordinator

UC San DiegoSan Diego, CA, United States
[job_card.temporary]
Gilman Drive, San Diego, CA 92093, United States.TP138562 Assistant Clinical Research Coordinator.Filing Deadline : Fri 2 / 27 / 2026. UC San Diego values and welcomes people from all backgrounds.If you ...[show_more][last_updated.last_updated_variable_days]
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Assistant Clinical Research Coordinator

Assistant Clinical Research Coordinator

University of California San DiegoSan Diego, CA, United States
[job_card.temporary]
MEDICINE / Cardiology Hiring Pay Scale.East Campus (La Jolla) Appointment Type : .Days, 8 hrs / day, Monday-Friday.Assistant Clinical Research Coordinator. UC San Diego values and welcomes people from all...[show_more][last_updated.last_updated_variable_days]
Clinical Research Coordinator

Clinical Research Coordinator

The Fountain GroupSan Diego, CA
[job_card.temporary]
Details for the position are as follows : .Conducts and coordinates tasks involved with the execution of the in-house clinical research projects in accordance with the clinical protocol, Clinical Aff...[show_more][last_updated.last_updated_30]
Clinical Research Coordinator- Bilingual

Clinical Research Coordinator- Bilingual

No-Resistance Consulting GroupSan Diego, CA, USA
[job_card.full_time]
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Candidates must be fluent in Spanish and English in both reading and writing in order to consent participants.Headquartered in Birmingham, No Resistance is a clinical trial site management organiza...[show_more][last_updated.last_updated_variable_days]
In-house Clinical Research Associate

In-house Clinical Research Associate

Solomon PageSan Diego, CA
[job_card.full_time]
A clinical-stage biopharmaceutical company in San Diego, California is seeking an experienced Contract Clinical Research Associate (CRA) to support ongoing clinical trials.This is an in-house clini...[show_more][last_updated.last_updated_30]
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Clinical Research Assistant - Biorepository - Per Diem - Grant Funded - Torrey Pines

Clinical Research Assistant - Biorepository - Per Diem - Grant Funded - Torrey Pines

Scripps HealthSan Diego, CA, United States
[job_card.full_time]
This is a casual / per diem, non-benefited position with day shifts, up to 20 hours / week.Hours would be Monday through Friday between the hours of 0800-1700. This position is grant funded through 9 / 20...[show_more][last_updated.last_updated_variable_days]
Senior Clinical Research Associate (West Coast-CA)

Senior Clinical Research Associate (West Coast-CA)

Alexion PharmaceuticalsUS,San Diego,CA
[job_card.full_time] +1
The Senior Clinical Research Associate (Sr.CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s).CRA works in clos...[show_more][last_updated.last_updated_variable_days]
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Clinical Research Assistant / Interviewer - French

Clinical Research Assistant / Interviewer - French

University of CaliforniaSan Diego, CA, United States
[job_card.full_time]
UCSD Layoff from Career Appointment.Apply by 2 / 4 / 2026 for consideration with preference for rehire.All layoff applicants should contact their Employment Advisor. Eligible Reassignment clients should...[show_more][last_updated.last_updated_variable_days]
Clinical Research Program Administrator – Alzheimer’s Clinical Trials Consortium–Down Syndrome (ACTC-DS)

Clinical Research Program Administrator – Alzheimer’s Clinical Trials Consortium–Down Syndrome (ACTC-DS)

Keck School of MedicineSan Diego, California
[job_card.full_time]
San Diego – hybrid work schedule.The Program Administrator will provide comprehensive administrative and programmatic support for the Alzheimer’s Clinical Trials Consortium–Down Syndrome (ACTC-DS),...[show_more][last_updated.last_updated_30]
Clinical Research Coordinator I

Clinical Research Coordinator I

CamrisSan Diego, CA, US
[job_card.full_time]
Clinical Research Coordinator I.Naval Health Research Center (NHRC), Operational Infectious Diseases (OID) Directorate.The OID Directorate conducts ongoing, laboratory-based surveillance of US mili...[show_more][last_updated.last_updated_variable_days]
Senior Clinical Research Director (SCRD)

Senior Clinical Research Director (SCRD)

Odyssey SystemsSan Diego, CA, US
[job_card.full_time]
ISR, C2, and warfighter readiness capabilities.Odyssey meets the military’s operational needs by integrating layered defense systems from equipment, technology, and services to data, information, a...[show_more][last_updated.last_updated_30]
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Research Associate

Research Associate

InsideHigherEdSan Diego, California, United States
[job_card.full_time]
New employees will begin on Step C ($5,557.Salary negotiation is not allowed.Promoted or transferred employees will be placed as specified in the CBA. This position is FLSA Non-exempt (may accrue ov...[show_more][last_updated.last_updated_variable_days]
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Clinical Logistics Manager

Clinical Logistics Manager

Artiva BiotherapeuticsSan Diego, CA, United States
[job_card.full_time]
Artiva is clinical-stage, publicly-traded biotechnology company focused on developing natural killer (NK) cell-based therapies for patients suffering from devastating autoimmune diseases and cancer...[show_more][last_updated.last_updated_variable_days]
Clinical-Scientific - Bench Scientist

Clinical-Scientific - Bench Scientist

MindlanceSan diego, CA
[job_card.full_time]
Clinical-Scientific - Bench Scientist.Troubleshoot and resolve technical issues with NMR spectrometers.Solve complex regio- and stereoisomer structures by NMR. Lead and coordinate NMR lab relocation...[show_more][last_updated.last_updated_30]
Cardiovascular Clinical Research Coordinator RN

Cardiovascular Clinical Research Coordinator RN

San Diego Cardiac Center Medical Group IncSan Diego, CA, USA
[job_card.full_time]
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The position of Cardiovascular Clinical Research Coordinator.Promotes the ethical conduct of research.Facilitates and coordinates the daily clinical trial activities and plays a critical role in th...[show_more][last_updated.last_updated_30]
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Clinical Psychologist On Site in Iwakuni or Sasebo, Japan

Clinical Psychologist On Site in Iwakuni or Sasebo, Japan

Arcetyp LLCSan Diego, CA, United States
[job_card.full_time] +1
Arcetyp LLC is a growing small business that provides a broad range of consulting services to US Federal Government, US Military, and Commercial clients. Services include Management & IT Consulting,...[show_more][last_updated.last_updated_variable_days]
Clinical Research Associate (Traumatic Brain Injury studies)

Clinical Research Associate (Traumatic Brain Injury studies)

GDITDiego, San, CA, USA
[job_card.full_time]
GDIT's Military Health Team is hiring a Clinical Research Associate to support clinical investigations for the Traumatic Brain Injury Center of Excellence (TBICoE) located at the Naval Medical Cent...[show_more][last_updated.last_updated_30]
Clinical Research Coordinator 1

Clinical Research Coordinator 1

MPF FederalSan Diego, CA, US
[job_card.30_days_ago]
[job_preview.job_type]
  • [job_card.full_time]
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[job_card.job_description]

MPF Federal seeks a Clinical Research Coordinator I to support the Naval Health Research Center (NHRC).

Compensation :   $68,000-$73,000 annually

Primary Responsibilities

  • Patient Recruitment and Consent : Identifies, and obtains informed consent from potential study participants in compliance with study protocols and ethical guidelines.
  • Help lead recruitment efforts, developing and refining strategies to meet enrollment targets.
  • Make independent decisions about how to target and select participants, and whether a potential participant meets eligibility criteria.
  • Manage and coordinate complex biosurveillance.
  • Study Protocol Design and Oversight : Interprets study protocols, assessing feasibility, and modifying procedures to align with the objectives of clinical trials.
  • Study Visits : Coordinates and conducts study visits, including patient interviews, sample collection, and other protocol-driven procedures.
  • Data Collection and Entry : Accurately collects, records, and manages study data. Ensures timely data entry into the Clinical Trial Management System (CTMS).
  • Data Analysis and Reporting : Interprets data to make recommendations on the direction of the research and adjusts study parameters based on preliminary findings.
  • Query Resolution : Works with the study team to resolve data queries and discrepancies in accordance with Good Clinical Practice (GCP) guidelines.
  • Compliance and Regulatory Decisions : Interprets and applies regulatory requirements, ensuring trials comply with legal, ethical, and institutional standards, and addressing issues without minimal supervision by the Clinical Program Manager.

Regulatory Management

  • Assists with Institutional Review Board (IRB) submissions and protocol amendments.
  • Collaborate with principal investigators and sponsors and provide insights based on field experience.
  • Recommend changes to improve study feasibility and evaluate the implications of protocol adjustments on ongoing activities.
  • Ensures compliance with all regulatory requirements, including study registrations in the electronic IRB (eIRB) system.

    • Compliance and Monitoring

  • Maintains accurate study documentation and ensures that study protocols are adhered to throughout the study lifecycle.
  • Ensure that the research team follows procedures. Troubleshoot and resolve any deviations or challenges that may arise.
  • Develop and implement quality control procedures, identify areas for improvement, and resolve any issues that could impact the validity or integrity of the study outcomes.
  • Prepares for and participates in monitoring visits, audits, and inspections by regulatory agencies.

    • Regulatory Responsibilities

  • Prepares and submits initial and continuing IRB applications, study amendments, and adverse event reports in compliance with NHRC and sponsor requirements.
  • Ensures all study-related documents are appropriately filed and accessible for audits.
  • Manages study registrations and updates in the Clinical Trial Management System and eIRB system.

    • Other Responsibilities

  • May be required to provide oversight and guidance to Assistant Clinical Research Coordinators and other support personnel.
  • Remote and On-Site Study Leadership :
  • Conduct research activities in varied environments, such as on naval ships or other remote sites, which may involve travel.
  • Coordinate logistics, including equipment and resource allocation, and serve as a research team representative on-site.
  • Make real-time decisions regarding study operations and troubleshoot unexpected scenarios to ensure study fidelity and safety.
  • Performs other duties as assigned.

    • Requirements

    Required

  • A BA / BS in biological sciences, public health, or equivalent OR five (5) plus years of infectious disease Biosurveillance experience.
  • Familiarity with regulatory requirements for clinical trials, including IRB submissions and reporting processes.
  • Proficiency in Clinical Trial Management Systems (CTMS) and electronic IRB systems.
  • Strong organizational, communication, and problem-solving skills.
  • Ability to work both independently and collaboratively in a research setting.
  • US Citizenship and the ability to obtain and maintain a T3 / Secret Clearance.

    • Preferred

  • Certification in clinical research (such as CCRC or CCRP).
  • Experience with infectious disease studies or military health research.

    • Benefits

    MPF Federal is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status or on the basis of disability. We offer a competitive compensation package including a competitive salary, medical benefits, PTO, holiday pay and more.