Top 50 Development coordinator Jobs in Turlock, 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
Activity Coordinator
CALIFORNIA PSYCHIATRIC TRANSITIONS —Delhi, CA
- $65,000 - $75,000 a year
- Full-time
- Psychiatry
- Mid-level
- Rehabilitation center
- Health insurance
- Dental insurance
Quick Apply
Training Coordinator
Modesto Irrigation District —Modesto, CA
- $99,694.40 - $127,628.80 a year
- Full-time
- Background check
- Writing skills
- Mid-level
Administrative Support Coordinator I
California State University —Turlock, CA
- Online Application
- Background check
- High school
- Writing skills
- Paid holidays
- Health insurance
2d
Grant Writer (Academic Coordinator II)
University of California Merced —Merced, CA
- $84,246 a year
- Full-time
- Mid-level
- Analysis skills
- University
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
Coordinator, Training
Saputo Inc. —Newman, CA
- $68,820 - $77,275 a year
- Email
- Classroom
- Microsoft Excel
- Bachelor of Science
- Employee stock ownership plan
- Retirement plan
10d
Staffing Coordinator
Doctors Medical Center of Modesto —Modesto, CA
- Per diem
- Acute care
- Psychiatry
- Hospital
- Health savings account
- Health insurance
1d
Reception Coordinator
Coffee Road Surgery Center, LLC (12516) —Modesto, CA
- $25 - $27 an hour
- Full-time
- Bilingual
- Surgery
- High school diploma or GED
Franchise Coordinator
Emergency Gear Direct —Ripon, CA
- Mid-level
Extra-Help Special Projects Coordinator
Merced County, CA —Merced County, CA
- $16.90 - $60.00 an hour
- Overtime
- System design
- Office
- IT
- Paid jury duty
- Paid holidays
9d
Program Coordinator (SSP IV)
California State University —Turlock, CA
- Weekends as needed
- Background check
- Doctoral degree
- Databases
- Paid holidays
- Health insurance
Program Coordinator (SSP IV)
California State University Stanislaus —Turlock, CA
- $6,320 - $9,014 a month
- Weekends as needed
- Background check
- Doctoral degree
- Databases
- Paid holidays
- Health insurance
Business Office Coordinator
Coffee Road Surgery Center, LLC (12516) —Modesto, CA
- $28.96 - $35.48 an hour
- Full-time
- Mid-level
- Office
- Administrative experience
- Free parking
- Health savings account
Marketing Events Coordinator
Bath Concepts Independent Dealers —Modesto, CA
- Weekends as needed
- Research
- Mid-level
- Recruiting
Quick Apply
Production Scheduler and Logistics Coordinator
SUPHERB FARMS —Turlock, CA
- $29.72 - $39.24 an hour
- ERP systems
- Pass drug screening
- Data analysis skills
Quick Apply
2d
Building Safety Program Coordinator
City of Modesto, CA —Modesto, CA
- $110,968.00 - $141,627.20 a year
- Overtime
- Word processing
- Research
- Mid-level
6d
Testing Initiative Coordinator
CALIFORNIA RURAL LEGAL ASSISTANCE INC —Modesto, CA
- $69,000 - $95,000 a year
- Full-time
- Hybrid work
- Mid-level
- Organizational skills
- Training & development
Quick Apply
Communications & Outreach Coordinator (Academic Coordinator 1)
University of California Merced —Merced, CA
- $64,228 a year
- Full-time
- Spanish
- English
- Mid-level
Office Coordinator
Maxim Healthcare —Modesto, CA
- $23 - $25 an hour
- Full-time
- HIPAA
- Office
- Administrative experience
- Profit sharing
- Commuter assistance
Quick Apply
13h

I want to receive the latest job alert for development coordinator in turlock, ca

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

development coordinator jobs near turlock, ca

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

development coordinator jobs in turlock, ca

Clinical Research Coordinator

Activity Coordinator

Training Coordinator

Administrative Support Coordinator I

Grant Writer (Academic Coordinator II)

Administrative Support Coordinator I

Coordinator, Training

Staffing Coordinator

Reception Coordinator

Franchise Coordinator

Extra-Help Special Projects Coordinator

Program Coordinator (SSP IV)

Program Coordinator (SSP IV)

Business Office Coordinator

Marketing Events Coordinator

Production Scheduler and Logistics Coordinator

Building Safety Program Coordinator

Testing Initiative Coordinator

Communications & Outreach Coordinator (Academic Coordinator 1)

Office Coordinator

I want to receive the latest job alert for development coordinator in turlock, ca

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected