Top 1268 Principal program Jobs in San Francisco, Ca

Clinical Research Coordinator
West Coast Retina Medical Group, Inc. —San Francisco, CA
- $25 - $50 an hour
- Full-time
- Patient monitoring
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Middle School Program Director
The Richmond Neighborhood Center —San Francisco, CA
- $123,600 - $129,780 a year
- Weekends as needed
- Background check
- School experience
- Classroom
- Health insurance
- Dental insurance
Quick Apply
Category Leader, Principal
PG&E Corporation —Oakland, CA
- $128,000 - $190,000 a year
- Hybrid work
- Master's degree
- 8 years
- Analysis skills
Principal Quality Operations Specialist
PG&E Corporation —Oakland, CA
- $125,000 - $226,000 a year
- Hybrid work
- PMP
- Bachelor of Science
- Office
23h
Principal Data Architect
Delta Dental —Oakland, CA
- $123,624 - $267,751 a year
- Full-time
- Hybrid work
- Background check
- Azure
- System design
- Paid holidays
- Health insurance
Administrative Assistant
University of California San Francisco —San Francisco, CA
- Full-time
- Internal Medicine
- Organizational skills
- Communication skills
9d
Shuttle Driver
University of California San Francisco —San Francisco, CA
- Full-time
- CDL B
- Background check
- Basic math
Program Manager, Principal- Short-Term Opportunity
Blue Shield of California —Oakland, CA
- $137,720 - $206,690 a year
- Full-time
- Hybrid work
- Background check
- 5 years
- Writing skills
- Dental insurance
- Work from home
3d
Principal, Internal Communications
ActBlue —San Francisco, CA
- $144,000 - $216,000 a year
- Full-time
- Remote
- Background check
- Travel
- Organizational skills
- AD&D insurance
- Disability insurance
1d
Principal Technical Program Manager
Early Warning Services —San Francisco, CA
- $206,000 - $258,000 a year
- Full-time
- Hybrid work
- Computer Science
- Pass drug screening
- Office
- Paid parental leave
- Health savings account
Health IT - Principal Trainer
University of California San Francisco —San Francisco, CA
- Full-time
- Computer science
- Computer Science
- Customer service
4d
Principal Program Manager
Intercom —San Francisco, CA
- $189,000 - $225,750 a year
- Hybrid work
- Office
- 8 years
- Mentoring
- Paid parental leave
- Health insurance
Staff/Principal Technical Program Manager
Rippling —San Francisco, CA
- $150,000 - $262,500 a year
- Full-time
- Hybrid work
- Computer science
- 7 years
- Computer Science
Principal Technical Program Manager
Hayden AI —San Francisco, CA
- $213,743 - $277,866 a year
- Full-time
- Hybrid work
- Bachelor of Science
- Office
- Machine learning
- Health insurance
- Dental insurance
Technical Program Manager, Principal
Blue Shield of California —Oakland, CA
- $137,720 - $206,690 a year
- Full-time
- Hybrid work
- Background check
- Engineering
- Pass drug screening
- Work from home
1d
Executive Protection Operator
OpenAI —San Francisco, CA
- $203,000 - $275,000 a year
- Full-time
- Hybrid work
- Office
- Residential
- Continuous improvement
- Flexible schedule
Safety Advisor
University of California San Francisco —San Francisco, CA
- 3 years
- University
- Bachelor's degree
Admitting Worker, Principal
University of California San Francisco —San Francisco, CA
- Monday to Friday
- Bilingual
- Computer literacy
- Writing skills
2d
Principal Regulatory Writer (Temporary)
Vir Biotechnology —San Francisco, CA
- $180 - $200 a day
- Temporary
- Remote
- 11+ years
- Project management
- Bachelor's degree
Quick Apply
8d
Principal Admitting Worker
University of California San Francisco —San Francisco, CA
- Bilingual
- Computer literacy
- Writing skills

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Clinical Research Coordinator

West Coast Retina Medical Group, Inc. -
San Francisco, CA

Quick Apply

Job Details

Full-time
$25 - $50 an hour

Benefits

Health insurance
Dental insurance
401(k)
Flexible spending account
Paid time off
Parental leave
Employee assistance program
Vision insurance
Employee discount
Professional development assistance
Flexible schedule
Life insurance
Retirement plan

Qualifications

Collaborate with healthcare professionals
Patient question and concern management
Clinical research
Electronic health records (EHR) management
Research ethical considerations
Research project coordination
Bachelor's degree
Clinical trials
Clinical quality assurance standards
Associate's degree
Documentation review
FDA regulations

Full Job Description

Position Summary:

The Clinical Research Coordinator (CRC) is responsible for the coordination and administration of clinical trials under the direction of the Clinical Research Manager, the Principal Investigator, and the Medical Director. The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials. The CRC will perform diverse administrative duties requiring analysis, sound judgment, and a high level of knowledge of study-specific protocols.

Duties and Responsibilities:

Administratively and clinically manage an average of four to five clinical trials

Adhere to research SOPs

Adhere to Good Clinical Practices and study protocols

Ensure the scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials

Discuss study protocols with patients and verify the information consent documentation

Provide patient with written communication of their participation (i.e. copy of the signed informed consent)

Ensure the patient’s referring physician receives the notification of the patient’s participation in studies as requested by the patient

Meet with the patient for each visit and maintain accessibility to discuss any questions/concerns regarding the study

Dispense study medication in a professional and accountable manner following protocol requirements

Collect, process, and ship blood/urine specimens at scheduled patient visits Perform ECGs and obtain vital signs of patients

Schedule all patient research visits and procedures consistent with the protocol requirements

Complete and maintain case report forms per FDA guidelines and review them against the patient’s medical record for completeness and accuracy

Administer questionnaires/diaries per protocol

Ensure that non-serious and serious adverse events are properly documented and reported

Screen laboratory results when received and follow protocol procedure regarding abnormal results

Ensure all laboratory results are given to appropriate doctors for review of clinical significance, then file results in the patient study binder

Submit patient reimbursement requests at the conclusion of patient’s participation in the protocol

Ensure the filing and maintenance of all regulatory documents

Schedule monitor visits and set up for monitoring visits before the monitor’s arrival

Participate in site assessments, pre-trial assessments, site initiation, subject recruitment and retention, monitoring, and close-out of clinical activities

Other duties as assigned

Education & Experience

Minimum associate degree in a health-related field

Minimum of two years of experience with clinical trial management

Qualifications & Requirements

Able to read, analyze, and interpret information from professional journals, technical procedures, or governmental regulations

Able to effectively present information and respond to questions from physicians, staff, and patients

Knowledge of Good Clinical Practices and the regulations necessary for the protection of human subjects and the conduct of clinical research required.

Knowledge of EHR systems

Able to function effectively in a team setting

Needs to demonstrate consistent professional conduct and meticulous attention to detail

Must possess excellent verbal and written communication skills as well as excellent interpersonal skills with patients, staff, and other health care professionals

Required to sit for CCRC after two years’ experience

Travel to any of the other West Coast Retina locations may be necessary upon request.

Travel within the USA for 2-3-day trips may be required for education conferences and networking events

Job Type: Full-time

Pay: $25.00 - $50.00 per hour

Benefits:

401(k)
Dental insurance
Employee assistance program
Employee discount
Flexible schedule
Flexible spending account
Health insurance
Life insurance
Paid time off
Parental leave
Professional development assistance
Retirement plan
Vision insurance

Education:

Bachelor's (Required)

Experience:

Clinical Trials Coordination: 3 years (Required)

Location:

San Francisco, CA 94109 (Preferred)

Ability to Commute:

San Francisco, CA 94109 (Required)

Work Location: In person

Quick Apply

Refine Your Search

principal program jobs in san francisco, ca

Clinical Research Coordinator

Middle School Program Director

Category Leader, Principal

Principal Quality Operations Specialist

Principal Data Architect

Administrative Assistant

Shuttle Driver

Program Manager, Principal- Short-Term Opportunity

Principal, Internal Communications

Principal Technical Program Manager

Health IT - Principal Trainer

Principal Program Manager

Staff/Principal Technical Program Manager

Principal Technical Program Manager

Technical Program Manager, Principal

Executive Protection Operator

Safety Advisor

Admitting Worker, Principal

Principal Regulatory Writer (Temporary)

Principal Admitting Worker

I want to receive the latest job alert for principal program in san francisco, ca

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