Top 75 Scientist 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
Research Associate
Certified Group —Turlock, CA
- $21 - $23 an hour
- Monday to Friday
- Microsoft Excel
- Computer literacy
- Bachelor of Science
Quick Apply
Research Data Scientist - AI Trainer
DataAnnotation —Aurora, CA
- $50.00 - $140.56 an hour
- Part-time
- Remote
- Computer Science
- English
- Mid-level
- Flexible schedule
Quick Apply
12d
Research Data Scientist - 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
Applied Scientist - AI Trainer
DataAnnotation —California
- $70.78 - $141.56 an hour
- Part-time
- Remote
- Computer Science
- Writing skills
- English
- Flexible schedule
Quick Apply
9d
Clinical Lab Scientist (CLS)
Emanuel Medical Ctr —Turlock, CA
- Full-time
- Acute care
- Hospital
- Mid-level
- Health savings account
- Health insurance
10d
QC Technician I
Sensient Technologies Corporation —Turlock, CA
- $24.80 an hour
- High school diploma or GED
- US work authorization
- Entry level
Clinical Laboratory Scientist, Float Pool
Sutter Health —Modesto, CA
- $66.15 - $92.61 an hour
- 8 hour shift
- Float pool
- Hospital
- Mid-level
As-Needed Lab Biologist
Dudek —Tracy, CA
- $31 an hour
- Part-time
- Microsoft Word
- Background check
- Microsoft Excel
- Employee assistance program
- Employee stock ownership plan
Seasonal Seed Health Lab Technician
Limagrain —Modesto, CA
- $18.50 - $23.00 an hour
- Seasonal
- Bachelor of Science
- Ability to lift 50 pounds
- Associate's degree
Clinical Lab Scientist (CLS)
Doctors Hospital of Manteca —Manteca, CA
- PRN
- Hospital
- Writing skills
- HIPAA
- Health savings account
- Health insurance
Process Validation Scientist
Certified Group —Turlock, CA
- $29 - $39 an hour
- Monday to Friday
- Microsoft Excel
- 3 years
- Analysis skills
Quick Apply
12d
FIELD ARCHAEOLOGISTS - (Southern California)
SummitWest Environmental —California
- $27 - $32 an hour
- Part-time
- Microsoft Word
- Background check
- Clean driving record
- Health insurance
- Dental insurance
Quick Apply
8d
FIELD ARCHAEOLOGISTS - (Central California)
SummitWest Environmental —California
- $27 - $32 an hour
- Part-time
- Microsoft Word
- Background check
- Clean driving record
- Health insurance
- Dental insurance
Quick Apply
7d
FIELD ARCHAEOLOGISTS - (Northern California)
SummitWest Environmental —California
- $27 - $32 an hour
- Part-time
- Microsoft Word
- Background check
- Clean driving record
- Health insurance
- Dental insurance
Quick Apply
8d
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
9d
Product Researcher (Dairy & Feed Expert)
Cattle Care —California
- $60,000 - $120,000 a year
- Part-time
- English
- Mid-level
- Analysis skills
Quick Apply
Marine Biologist
AIS Inc —California
- $5,100 - $8,100 a month
- Full-time
- Heavy lifting
- Laboratory experience
- Mid-level
- Paid training
- Health savings account
Quick Apply
Tribal NEPA Specialist
Onterris —California
- $70,500 - $95,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Analysis skills
Manager Environmental Services
Global Medical Response —California
- $102,000 - $115,000 a year
- Full-time
- Project management
- Bachelor's degree
- Travel

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scientist jobs near modesto, 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

scientist jobs in modesto, ca

Clinical Research Coordinator

Research Associate

Research Data Scientist - AI Trainer

Research Data Scientist - AI Trainer

Applied Scientist - AI Trainer

Clinical Lab Scientist (CLS)

QC Technician I

Clinical Laboratory Scientist, Float Pool

As-Needed Lab Biologist

Seasonal Seed Health Lab Technician

Clinical Lab Scientist (CLS)

Process Validation Scientist

FIELD ARCHAEOLOGISTS - (Southern California)

FIELD ARCHAEOLOGISTS - (Central California)

FIELD ARCHAEOLOGISTS - (Northern California)

Clinical Data Scientist - AI Trainer

Product Researcher (Dairy & Feed Expert)

Marine Biologist

Tribal NEPA Specialist

Manager Environmental Services

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