Top 26 Phlebotomy Jobs in Oakdale, 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
Certified Phlebotomy Technician (CPT) Laboratory Assistant II
Sutter Health —Modesto, CA
- $27.98 - $39.17 an hour
- 8 hour shift
- Mid-level
- High school diploma or GED
- Computer skills
Phlebotomist
Doctors Hospital of Manteca —Manteca, CA
- Per diem
- Hospital
- Critical & Intensive Care
- Organizational skills
- Health savings account
- Health insurance
9h
Certified Phlebotomy Technician
Ansible Government Solutions —Modesto, CA
- $23.56 - $28.49 an hour
- Full-time
- OSHA
- Clinic experience
- Mid-level
Quick Apply
Certified Phlebotomy Technician (CPT) Laboratory Assistant II, Float Pool
Sutter Health —Modesto, CA
- $29.25 - $40.95 an hour
- 8 hour shift
- Float pool
- Hospital
- Mid-level
Plasma Center Technician
Biolife Plasma Services —Modesto, CA
- From $19 an hour
- Part-time
- Vital signs
- Ability to walk for extended periods
- High school diploma or GED
- Paid training
- Paid holidays
Mobile Phlebotomist (Sacramento)
TruArc Health —Modesto, CA
- $22 - $26 an hour
- Part-time
- OSHA
- HIPAA
- Clinic experience
Quick Apply
Mobile Phlebotomist (Independent Contractor)
Biodesix, Inc. —Modesto, CA
- Contract
- Computer skills
- Reliable transportation
- Communication skills
Quick Apply
Lead Mobile Phlebotomist
TridentCare —Manteca, CA
- $21 - $23 an hour
- Clean driving record
- Nursing home
- English
Phlebotomist II Float
Quest Diagnostics —Modesto, CA
- $26.05 - $28.45 an hour
- Full-time
- Private practice
- Customer service
- English
- Employee stock purchase plan
- Disability insurance
Quick Apply
Lab Assistant Lead
Sutter Health —Modesto, CA
- $37.47 - $52.45 an hour
- 8 hour shift
- Anatomy knowledge
- Microsoft Outlook
- Hospital
Medical Laboratory Technician
Sutter Health —Modesto, CA
- $48.03 - $67.23 an hour
- Full-time
- Hospital
- Computer literacy
- Mid-level
Phlebotomy (CPT-1) Didactic Instructor
First Lady Permanente, LLC Education Center —Turlock, CA
- $29 - $32 an hour
- Part-time
- Background check
- Laboratory
- Classroom
- Flexible schedule
Quick Apply
5d
Clinical Laboratory Scientist, Float Pool
Sutter Health —Modesto, CA
- $66.15 - $92.61 an hour
- 8 hour shift
- Float pool
- Hospital
- Mid-level
CT Tech Trainee
NorCal Imaging Centers —Modesto, CA
- $40 - $50 an hour
- Full-time
- BLS Certification
- HIPAA
- Clinic
- Health savings account
- Health insurance
CT Technologist | Bonus + Relocation to Longview, Washington!
PeaceHealth —United States
- $44.29 - $66.93 an hour
- 12 hour shift
- Acute care
- Background check
- Hospital
- Continuing education credits
- 403(b) matching
Quick Apply

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Certified Phlebotomy Technician (CPT) Laboratory Assistant II
Sutter Health —Modesto, CA
Adheres to all local/state/federal regulations, codes, policies and procedures to ensure privacy and safety while delivering optimal patient care.
$27.98 - $39.17 an hour
Certified Phlebotomy Technician (CPT) Laboratory Assistant II, Float Pool
Sutter Health —Modesto, CA
Adheres to all local/state/federal regulations, codes, policies and procedures to ensure privacy and safety while delivering optimal patient care.
$29.25 - $40.95 an hour

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Hometown Urgent Care —Canal Winchester, OH
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Valid Drivers' license with a minimum of 1 year driving experience. Performs basic clerical duties, i.e. filing, faxing, and preparing mail.
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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

phlebotomy jobs in oakdale, ca

Clinical Research Coordinator

Certified Phlebotomy Technician (CPT) Laboratory Assistant II

Phlebotomist

Certified Phlebotomy Technician

Certified Phlebotomy Technician (CPT) Laboratory Assistant II, Float Pool

Plasma Center Technician

Mobile Phlebotomist (Sacramento)

Mobile Phlebotomist (Independent Contractor)

Lead Mobile Phlebotomist

Phlebotomist II Float

Lab Assistant Lead

Medical Laboratory Technician

Phlebotomy (CPT-1) Didactic Instructor

Clinical Laboratory Scientist, Float Pool

CT Tech Trainee

CT Technologist | Bonus + Relocation to Longview, Washington!

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