Top 9461 Science general Jobs

Clinical Research Coordinator
Paradigm Clinical Research Center —Modesto, CA
- $55,000 - $65,000 a year
- Part-time
- Background check
- Mid-level
- Master's degree
- Health insurance
- Dental insurance
Quick Apply
Organizational Psychologist
Central Intelligence Agency —Washington, DC
- $179,891 - $288,000 a year
- Full-time
- 5 years
- Doctor of Philosophy
- Travel
- Health insurance
- Dental insurance
Associate Director, Ingredient Development
HelloFresh —New York, NY
- $140,700 - $190,000 a year
- Full-time
- Google Workspace
- 8 years
- Analysis skills
- Health insurance
- Tuition reimbursement
Medical Laboratory Scientist - Weekend Overnight
MedStar Health —Baltimore, MD
- $35.68 - $64.71 an hour
- Part-time
- Mid-level
- Computer skills
- Associate's degree
Medical Laboratory Scientist Non-Certified - Rapid Response Laboratory - Evening
Wellspan Health —Lebanon, PA
- Full-time
- Acute care
- Surgery
- Hospital
- Paid parental leave
- Health insurance
Research Associate, Healthcare Innovations
American Institutes for Research —Remote
- $33 - $40 an hour
- Email
- Remote
- Mid-level
- Business development experience
- Bachelor's degree
Research Assistant
University of California San Francisco —San Francisco, CA
- Internal Medicine
- University
- Bachelor's degree
General Interest
Guide Labs —San Francisco, CA
- Full-time
- Hybrid work
- Entry level
Quick Apply
Research Technician I, Biochemistry
UT Southwestern —Dallas, TX
- Full-time
- High school diploma or GED
- Assembly
- Bachelor's degree
- Paid parental leave
- Paid holidays
Biostatistician/Modeler (Epidemiology)
Johns Hopkins University —Baltimore, MD
- $55,800 - $97,600 a year
- Full-time
- Background check
- Mid-level
- Office
Research Associate (General)
Harvard University —Boston, MA
- Full-time
- Hybrid work
- Writing skills
- Mid-level
- Analysis skills
- Commuter assistance
- Health insurance
Scientist
Meso Scale Diagnostics, LLC. —Gaithersburg, MD
- $101,400 - $154,700 a year
- Microsoft Excel
- Microsoft Outlook
- Public speaking
- Paid parental leave
- AD&D insurance
Quick Apply
Early Career Researchers - Research Associate I, Broad-wide openings
Broad Institute —Cambridge, MA
- $50,000 - $70,000 a year
- Overtime
- In-person
- 1 year
- Entry level
- Health savings account
- Paid holidays
Biology Scientist
Apostle —Pleasanton, CA
- $75,000 - $110,000 a year
- Full-time
- No experience needed
- Doctor of Philosophy
- In-person
ENVIRONMENTAL SCIENTIST
Department of Forestry & Fire Protection —Yolo County, CA
- $4,418 - $9,321 a month
- Overtime
- Hybrid work
- Doctoral degree
- Mid-level
- Office
- Opportunities for advancement
9d
Assistant Geologist
Terracon —Carson, CA
- $26.75 - $37.50 an hour
- Driver's License
- Bachelor's degree
- Military encouraged
- Paid holidays
- Health insurance
Research Technician
California Institute of Technology —Pasadena, CA
- $19.00 - $25.75 an hour
- Overtime
- University
- Bachelor's degree
- Organizational skills
Laboratory Technician
Soil Culture Solutions, LLC (d/b/a Soilcea) —Tampa, FL
- $16 - $23 an hour
- Full-time
- Maintenance
- Research
- In-person
- Health insurance
- Paid time off
Quick Apply
Research Technician
Virginia Tech —Washington, DC
- Overtime
- Project management
- University
- Organizational skills
Research Specialist C
University of Pennsylvania —Philadelphia, PA
- $58,506.00 - $67,794.79 a year
- Full-time
- Background check
- Bachelor of Science
- Mid-level
- Health insurance
- Dental insurance

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Clinical Research Coordinator

Paradigm Clinical Research Center -
Modesto, CA

Quick Apply

Job Details

Part-time | Full-time
$55,000 - $65,000 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: $55,000.00 - $65,000.00 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

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Clinical Research Coordinator

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