Top 1851 Project Jobs in Modesto, Ca

Clinical Research Coordinator
Paradigm Clinical Research Center —Modesto, CA
- $65,000 - $70,000 a year
- Part-time
- Background check
- Mid-level
- Master's degree
- Health insurance
- Dental insurance
Quick Apply
Purchasing Specialist / Accounts Payable
Cal-Cat Industries —Hughson, CA
- $22 - $25 an hour
- Overtime
- Spanish
- Inventory management
- English
- Health insurance
- Dental insurance
Quick Apply
12d
Research Associate
Certified Group —Turlock, CA
- $21 - $23 an hour
- Monday to Friday
- Microsoft Excel
- Computer literacy
- Bachelor of Science
Quick Apply
AI Data Quality Specialist - AI Trainer
DataAnnotation —Aurora, CA
- $50.00 - $140.56 an hour
- Part-time
- Remote
- Computer Science
- English
- Mid-level
- Flexible schedule
Quick Apply
12d
AI Data Quality Specialist - AI Trainer
DataAnnotation —Sherwood Park, CA
- $50.00 - $140.56 an hour
- Part-time
- Remote
- Computer Science
- English
- Mid-level
- Flexible schedule
Quick Apply
12d
R5: Construction Laborer- Project Based- San Joaquin Valley
Essel —Modesto, CA
- $40,000 - $52,000 a year
- Overtime
- Construction site
- Entry level
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Project Coordinator EBS
Elite Builder Services —Modesto, CA
- $20 - $22 an hour
- Full-time
- Google Workspace
- Inventory management
- Computer literacy
Quick Apply
CSR/Project Specialist
Cencal Mechanical Heating & Air, Inc —Modesto, CA
- $20 - $26 an hour
- Full-time
- Office
- High school diploma or GED
- In-person
- Health insurance
- Paid time off
Quick Apply
10d
Administrative Assistant
BEAM Circular —Modesto, CA
- $54,995 - $67,995 a year
- Full-time
- Hybrid work
- Mid-level
- Office
- Driving
- Work from home
- Professional development assistance
Quick Apply
11d
Administrative Assistant
Sysco —Modesto, CA
- $21.20 - $31.78 an hour
- Microsoft Outlook
- Writing skills
- English
17h
Administrative Services Technician I/II
City of Modesto, CA —Modesto, CA
- $29.65 - $41.77 an hour
- Overtime
- Word processing
- Office
- Finance
14d
Innovation Campus Project Associate
BEAM Circular —Modesto, CA
- $60,000 - $80,000 a year
- Full-time
- Hybrid work
- Mid-level
- Office
- Analysis skills
Quick Apply
Administrative Support Coordinator I
California State University Stanislaus —Turlock, CA
- $4,047 - $5,896 a month
- Online Application
- Background check
- High school
- Writing skills
- Paid holidays
- Health insurance
2d
Executive Assistant - Modesto, CA
The Save Mart Companies —Modesto, CA
- $23.13 - $30.36 an hour
- Overtime
- No high school diploma
- Research
- Mid-level
- AD&D insurance
- Health insurance
Quick Apply
8d
Executive Assistant
HOGAN MFG INC —Escalon, CA
- $70,304 - $95,000 a year
- Microsoft Excel
- Microsoft Outlook
- 5 years
Quick Apply
Dispatcher
Tonys Plumbing Heating & Air LP —Modesto, CA
- $22 - $26 an hour
- Weekends as needed
- Administrative experience
- Typing
- In-person
- Paid training
- Paid holidays
Quick Apply
7d
Program Coordinator II, Diagnostic Imaging Scheduling
Sutter Health —Modesto, CA
- $27.85 - $38.99 an hour
- 8 hour shift
- Microsoft Outlook
- Computer literacy
- High school diploma or GED
UNIT CLERK
Central Valley Specialty Hospital —Modesto, CA
- Part-time
- Hospital
- Writing skills
- BLS Certification
Sales Associate
Ace Hardware —Modesto, CA
- 8 hour shift
- No education required
- Sales
- Ability to lift 50 pounds
- Health insurance
- Dental insurance
Quick Apply
Marketing Communications Specialist
Valley First Credit Union —Modesto, CA
- $32 - $42 an hour
- Full-time
- 7 years
- Marketing
- Office

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Clinical Research Coordinator

Paradigm Clinical Research Center -
Modesto, CA

Quick Apply

Job Details

Part-time | Full-time
$65,000 - $70,000 a year

Benefits

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

Qualifications

CCRC
Phlebotomy
Organizational skills
Pediatrics

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.

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.

Experience

CCRC Required.
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.

Job Types: Full-time, Part-time

Pay: $65,000.00 - $70,000.00 per year

Benefits:

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

Ability to Commute:

Modesto, CA 95357 (Required)

Work Location: In person

Quick Apply

Refine Your Search

project jobs in modesto, ca

Clinical Research Coordinator

Purchasing Specialist / Accounts Payable

Research Associate

AI Data Quality Specialist - AI Trainer

AI Data Quality Specialist - AI Trainer

R5: Construction Laborer- Project Based- San Joaquin Valley

Project Coordinator EBS

CSR/Project Specialist

Administrative Assistant

Administrative Assistant

Administrative Services Technician I/II

Innovation Campus Project Associate

Administrative Support Coordinator I

Executive Assistant - Modesto, CA

Executive Assistant

Dispatcher

Program Coordinator II, Diagnostic Imaging Scheduling

UNIT CLERK

Sales Associate

Marketing Communications Specialist

I want to receive the latest job alert for project in modesto, ca

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