Top 26362 Assistant program coordinator 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
Nitrogen Assistant Coordinator/Dispatcher
Copper Tip Energy Services Inc —Williston, ND
- $90,000 - $120,000 a year
- Full-time
- Background check
- Management
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Credentialing Coordinator
Alumni Healthcare Staffing —Bridgewater, NJ
- From $48,000 a year
- Full-time
- Hybrid work
- Background check
- Customer service
- Word processing
- Paid holidays
- Health insurance
Quick Apply
Assistant Director of Training
Local 290 Training Center —Tualatin, OR
- $3,571.60 a week
- Full-time
- Mid-level
- Office
- Ability to lift 50 pounds
- Health insurance
- Dental insurance
Quick Apply
Student Program Coordinator
Clinic for the Rehabilitation of Wildlife —Sanibel, FL
- Email
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Intake Assistant
Services For The Underserved, Inc. —New York, NY
- $55,000 - $60,000 a year
- Full-time
- Remote
- Writing skills
- Office
- Residential
- Paid time off
Program Implementation Coordinator
AMOpportunities —Remote
- $55,000 - $65,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Customer service
- Commuter assistance
- Loan repayment program
Quick Apply
Program Coordinator / Executive Assistant
CGC —Washington, DC
- $117,715 - $132,549 a year
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- 401(k)
Quick Apply
Program Coordinator
NYU Langone Health —New York, NY
- $66,300 - $71,380 a year
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Wellness program
Assistant Program Coordinator - School of Medicine Neurobehavior
Emory University —Atlanta, GA
- Full-time
- Hybrid work
- Research
- Databases
- University
Faculty Assistant and Program Coordinator
Harvard University —Cambridge, MA
- Full-time
- Hybrid work
- Google Workspace
- Microsoft Outlook
- Customer service
- Travel reimbursement
- Commuter assistance
Practice Assistant
K&L Gates —Washington, DC
- $79,000 - $119,000 a year
- Overtime
- Remote
- Background check
- Microsoft Outlook
- Addiction Medicine
- Profit sharing
- Wellness program
HR Coordinator / Administrative Assistant
Rose Cartage Service, Inc. —Griffith, IN
- $22 - $25 an hour
- Online Application
- Background check
- Writing skills
- Pass drug screening
- Health insurance
- 401(k)
Quick Apply
Research Administrative Coordinator
Cardiovascular Associates of America —Remote
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Customer service
Quick Apply
Community and Citizenship Assistant Coordinator
Turner Construction Company —New York, NY
- $80,000 - $90,000 a year
- Microsoft Outlook
- Marketing
- Mid-level
Program Coordinator
Georgetown University —Washington, DC
- $20.16 - $31.30 an hour
- Full-time
- Mid-level
- University
- Bachelor's degree
- Disability insurance
- Health insurance
13d
Program Coordinator
Harvard University —Cambridge, MA
- Overtime
- Hybrid work
- Public speaking
- Mid-level
- Office
- Commuter assistance
- Health insurance
Academic Program Assistant
USC —Los Angeles, CA
- $25.32 - $33.95 an hour
- Hybrid work
- Psychiatry
- Customer service
- Mid-level
Regulatory Coordinator Assistant
RCCA MSO LLC —Teaneck, NJ
- $27.09 - $36.54 an hour
- Full-time
- Microsoft Word
- Mid-level
- High school diploma or GED
- Wellness program
- Health savings account
Quick Apply
Assistant Coordinator
Carnival Cruise Line —Miami, FL
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Employee stock purchase plan
- Paid holidays

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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

assistant program coordinator jobs

Clinical Research Coordinator

Nitrogen Assistant Coordinator/Dispatcher

Credentialing Coordinator

Assistant Director of Training

Student Program Coordinator

Intake Assistant

Program Implementation Coordinator

Program Coordinator / Executive Assistant

Program Coordinator

Assistant Program Coordinator - School of Medicine Neurobehavior

Faculty Assistant and Program Coordinator

Practice Assistant

HR Coordinator / Administrative Assistant

Research Administrative Coordinator

Community and Citizenship Assistant Coordinator

Program Coordinator

Program Coordinator

Academic Program Assistant

Regulatory Coordinator Assistant

Assistant Coordinator

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