Top 201 Clinical trials 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
Clinical Data Scientist - AI Trainer
DataAnnotation —California
- $70.78 - $141.56 an hour
- Part-time
- Remote
- Computer Science
- Writing skills
- English
- Flexible schedule
Quick Apply
11d
Special Agent: Healthcare Services/Medical Background
Federal Bureau of Investigation —San Diego, CA
- $103,326 - $133,200 a year
- Full-time
- Research
- Mid-level
- Bachelor's degree
Clinical Research Coordinator
Medical Research Team- San Diego —San Diego, CA
- $30 - $75 an hour
- Part-time
- Hybrid work
- Mid-level
- Analysis skills
- Supervising experience
- Tuition reimbursement
- Professional development assistance
Quick Apply
1d
Clinical Research Associate
USC —San Diego, CA
- $36.36 - $50.90 an hour
- Background check
- Mid-level
- Bachelor's degree
Associate Specialist, Clinical Trials Operations
Neurocrine Bioscience —San Diego, CA
- $35.35 - $47.34 an hour
- Full-time
- Psychiatry
- Computer literacy
- Bachelor of Science
- Paid holidays
- Health 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
7d
Clinical Research Coordinator I
CAMRIS International, LLC —San Diego, CA
- $70,304 - $73,000 a year
- Full-time
- 5 years
- Bachelor of Science
- Mid-level
- Health savings account
- AD&D 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
11d
Clinical Research Assistant - Oncology
Scripps Health —La Jolla, CA
- $28.05 - $37.65 an hour
- Full-time
- Hospital
- Bachelor of Science
- BLS Certification
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
Clinical Research Coordinator (Non-RN) - Hematology/Oncology Research Resources
Rady Children's Health —San Diego, CA
- $34.14 - $46.94 an hour
- Vital signs
- Management
- Word processing
Clinical Research Coordinator
ALLIANCE CLINICAL LLC —San Diego, CA
- $28 - $30 an hour
- Temporary
- CPR Certification
- Microsoft Excel
- BLS Certification
Quick Apply
13h
Associate Manager / Manager, Project Services - Laboratories (Remote - West Coast)
IQVIA —San Diego, CA
- $64,200 - $173,000 a year
- Full-time
- Remote
- Microsoft Excel
- Computer literacy
- Data analysis skills
- Work from home
Clinical Research Coordinator
Medical Oncology Associates of San Diego —San Diego, CA
- $70,000 - $80,000 a year
- 8 hour shift
- Patient monitoring
- Bachelor of Science
- HIPAA
- Health insurance
- Dental insurance
Quick Apply
Assistant Research Administrator
USC —San Diego, CA
- $36.94 - $47.00 an hour
- Background check
- Microsoft Excel
- Microsoft Access
Senior Clinical Research Associate (level dependent on experience)
CTI Clinical Trial Services, Inc —San Diego, CA
- Hybrid work
- Nursing
- Mid-level
- Master's degree
- Paid parental leave
- Tuition reimbursement
Quick Apply
Clinical Research Coordinator
Odyssey Consulting —Naval Medical Center San Diego, CA
- $80,000 - $90,793 a year
- Weekends as needed
- Hybrid work
- Mid-level
- Office
- 3 years
- Health savings account
- Paid holidays
14d
Staff Research Associate- PATHOLOGY
UC San Diego Health —San Diego, CA
- $30.12 - $35.93 an hour
- 8 hour shift
- Microsoft Excel
- Pass drug screening
- English
7d
Clinical Research Coordinator
Erick H Alayo —Chula Vista, CA
- $25 - $40 a year
- Part-time
- Spanish
- Patient monitoring
- Mid-level
Quick Apply
11d

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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

clinical trials jobs in san diego ca

Clinical Research Coordinator

Clinical Data Scientist - AI Trainer

Special Agent: Healthcare Services/Medical Background

Clinical Research Coordinator

Clinical Research Associate

Associate Specialist, Clinical Trials Operations

Assistant Clinical Research Coordinator - Psych

Clinical Research Coordinator I

Research Assistant - Medicine

Clinical Research Assistant - Oncology

Anxiety and Stress Staff Research Associate

Clinical Research Coordinator (Non-RN) - Hematology/Oncology Research Resources

Clinical Research Coordinator

Associate Manager / Manager, Project Services - Laboratories (Remote - West Coast)

Clinical Research Coordinator

Assistant Research Administrator

Senior Clinical Research Associate (level dependent on experience)

Clinical Research Coordinator

Staff Research Associate- PATHOLOGY

Clinical Research Coordinator

I want to receive the latest job alert for clinical trials in san diego ca

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