Top 113 Background investigator Jobs in San Diego Ca

Clinical Research Coordinator
Paradigm Clinical Research Center —San Diego, CA
- $60,000 - $75,000 a year
- Temporary
- Background check
- Mid-level
- Master's degree
- Health insurance
- Dental insurance
Quick Apply
Public Health Field Investigator
Council For Logistics Research Inc —San Diego, CA
- $85,000 - $105,000 a year
- Full-time
- Nursing
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
Research Assistant - Medicine
UC San Diego Health —San Diego, CA
- $30.12 - $35.93 an hour
- 8 hour shift
- Word processing
- Pass drug screening
- Mid-level
5d
Assistant Research Administrator
USC —San Diego, CA
- $36.94 - $47.00 an hour
- Background check
- Microsoft Excel
- Microsoft Access
Anxiety and Stress Staff Research Associate
UC San Diego Health —San Diego, CA
- $30.12 - $35.93 an hour
- 8 hour shift
- Microsoft Excel
- Psychiatry
- Pass drug screening
Genetics Staff Research Associate - Psychiatry
UC San Diego Health —San Diego, CA
- $30.12 - $35.93 an hour
- Part-time
- Remote
- Microsoft Excel
- Psychiatry
- Addiction Medicine
8d
Animal Health Tech I
Salk Institute for Biological Studies —La Jolla, CA
- $17.75 - $20.00 an hour
- Weekends as needed
- Current TB test
- No experience needed
- High school diploma or GED
- Health insurance
- Dental insurance
Clinical Trials Research Assistant - Medicine
UC San Diego Health —San Diego, CA
- $26.23 - $33.13 an hour
- 8 hour shift
- Microsoft Word
- Microsoft Excel
- Pass drug screening
Lab Assistant II - Psychiatry
UC San Diego Health —San Diego, CA
- $27.54 - $33.13 an hour
- 8 hour shift
- Spanish
- Microsoft Excel
- Psychiatry
6d
Communicable Disease Investigator
County of San Diego —San Diego, CA
- $68,619.20 - $84,281.60 a year
- Full-time
- Background check
- CPR Certification
- LVN
4d
Safety & Security Investigator
Marriott International, Inc —Chula Vista, CA
- $27.75 an hour
- Part-time
- CPR Certification
- BLS Certification
- Mid-level
Staff Research Associate 1
UC San Diego —San Diego, CA
- $30.12 - $35.93 an hour
- Overtime
- Background check
- Bachelor of Science
- Maintenance
13d
Program Coordinator I
San Diego State University Research Foundation —San Diego, CA
- $5,875 a month
- Full-time
- Remote
- Background check
- Spanish
- 5 years
Research Administrative Assistant
VENESCO, LLC —San Diego, CA
- $24 - $29 an hour
- Full-time
- Hybrid work
- Background check
- Microsoft Excel
- Microsoft Outlook
Quick Apply
Executive Operations Coordinator - ACTRI - Hybrid
UC San Diego Health —San Diego, CA
- $32.75 - $50.62 an hour
- 8 hour shift
- Hybrid work
- Writing skills
- Pass drug screening
- Mid-level
- Travel reimbursement
9d
Research Administrator 2
UC San Diego —San Diego, CA
- $35.99 - $52.42 an hour
- Overtime
- Hybrid work
- Background check
- Oracle
- Mid-level
14d
Research Assistant I - Dr. Thales Papagiannakopoulos
Salk Institute for Biological Studies —La Jolla, CA
- $18 - $21 an hour
- Analysis skills
- Bachelor's degree
- 2 years
- Health insurance
- Dental insurance
Assistant Clinical Research Coordinator - Psych
UC San Diego Health —San Diego, CA
- $36.31 - $58.41 an hour
- 8 hour shift
- Microsoft Word
- Psychiatry
- Addiction Medicine
1d
Social Media Investigator
Digistream Investigations —San Diego, CA
- $22 an hour
- Full-time
- Communication skills
- Entry level
- Health insurance
- Dental insurance
Quick Apply
4d
RESEARCH TECHNICIAN - Lippi Lab
Scripps Research —San Diego, CA
- $18.67 - $24.00 an hour
- 3 years
- Bachelor's degree
- Entry level
- Free parking
- Health savings account

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Clinical Research Coordinator

Paradigm Clinical Research Center -
San Diego, CA

Quick Apply

Job Details

Temporary | Part-time | Full-time
$60,000 - $75,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance

Qualifications

CCRC
Clinical research

Full Job Description

Overview
We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team. This role is integral to the successful execution of clinical trials, ensuring that all research activities are conducted in compliance with regulatory standards and Good Clinical Practice (GCP). The ideal candidate will have a strong background in clinical research and possess excellent organizational skills to manage various aspects of study coordination. This role may require occasional local travel between clinic locations.

Responsibilities

Coordinate clinical research studies from start to finish, including study start-up, recruitment, screening, enrollment, treatment, follow-up, and close-out.
Develop and maintain study documents, including study protocols, informed consent forms, case report forms, and study manuals.
Obtain and maintain regulatory approvals, including Institutional Review Board (IRB) approvals and other required regulatory documentation.
Screen and enroll eligible study participants according to study protocols and ensure that participants receive appropriate study treatments and follow-up care.
Collect and manage study data using electronic data capture systems and ensure the accuracy and completeness of study data
Develop and maintain study databases, conduct quality control checks, and generate study reports as required.
Work closely with study sponsors and other stakeholders to ensure the successful completion of clinical research studies.
Train and supervise research staff, including research assistants and volunteers, and ensure compliance with study protocols and regulatory requirements.
Communicate study progress and results to study sponsors, regulatory authorities, and other stakeholders.
Participate in the development and implementation of new clinical research studies and initiatives.
Coordinate study activities with other departments and external partners.
Monitor study progress and works to identify research related issues and discrepancies when evident, and appropriately escalates to site manager, director, or investigator for resolution as needed.
Ensure compliance with study protocols, GCP guidelines, and regulatory requirements.
Train and supervise junior research staff as required.
Assist with collecting training forms, collection and or preparation of essential documents and obtaining required signatures from all applicable research personnel for regulatory/essential documents throughout the duration of a study including, but not limited, to Food and Drug administration (FDA) form 1572, CV, professional licensure, financial disclosure form (FDF), and Institutional Review Board (IRB) submission forms.
Communicate with study participants and their families to provide study-related information and to ensure study visit schedules are met.
Adheres to standard operating procedures (SOP).
Participate in study team meetings and attend required training and educational sessions.
Maintain study supplies and equipment and ensure that they are stored and maintained in accordance with regulatory requirements.
Trains under the guidance of direct supervisor and other site personnel to promote participation in research studies including mail-outs and other marketing programs as applicable.
Assist with general managed site projects and workload sharing as assigned by direct supervisor.
Travel locally between clinic locations as needed to support study operations.

Experience

CCRC Preferred
Bachelor or master’s degree in a health-related field such as biology, or public health
preferred.
Proficient knowledge of GCP guidelines, regulatory requirements, and clinical trial
operations
> 4 years’ experience working in clinical research environment.
Excellent organizational and communication skills.
Ability to work independently and as part of a team.
Strong organizational skills and attention to detail, with the ability to manage multiple tasks and priorities simultaneously.
Excellent communication skills, with the ability to communicate effectively with study sponsors, regulatory authorities, research staff, and study participants.
Proficient in the use of electronic data capture systems and database management tools.
Ability to work independently and as part of a team in a fast-paced, deadline-driven environment.
Willingness to learn new skills and take on new responsibilities as needed.

If you are passionate about advancing medical research and have the necessary skills to excel as a Clinical Research Coordinator, we encourage you to apply for this exciting opportunity.

Pay: $60,000.00 - $75,000.00 per year

Benefits:

401(k)
Dental insurance
Health insurance
Paid time off
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

background investigator jobs in san diego ca

Clinical Research Coordinator

Public Health Field Investigator

Research Assistant - Medicine

Assistant Research Administrator

Anxiety and Stress Staff Research Associate

Genetics Staff Research Associate - Psychiatry

Animal Health Tech I

Clinical Trials Research Assistant - Medicine

Lab Assistant II - Psychiatry

Communicable Disease Investigator

Safety & Security Investigator

Staff Research Associate 1

Program Coordinator I

Research Administrative Assistant

Executive Operations Coordinator - ACTRI - Hybrid

Research Administrator 2

Research Assistant I - Dr. Thales Papagiannakopoulos

Assistant Clinical Research Coordinator - Psych

Social Media Investigator

RESEARCH TECHNICIAN - Lippi Lab

I want to receive the latest job alert for background investigator in san diego ca

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