Top 106 Head collection development Jobs in Los Angeles, Ca

Clinical Research Coordinator II – Head & Neck (Hybrid Role)
CEDARS-SINAI —Beverly Hills, CA
- Full-time
- Hybrid work
- HIPAA
- Mid-level
- High school diploma or GED
Facilities Coordinator
Housing Authority City of Los Angeles —Los Angeles, CA
- $95,305.60 - $117,228.80 a year
- Full-time
- Writing skills
- Mid-level
- Office
- Disability insurance
- Health insurance
Service Area Supervisor
Pacific Clinics —Los Angeles, CA
- From $71,760 a year
- Classroom
- CPR Certification
- Bachelor of Science
- Health insurance
- Dental insurance
CSPP Program Specialist
Human Services Association —South Gate, CA
- $37 - $41 an hour
- Weekends as needed
- Background check
- CPR Certification
- Management
- Health insurance
- Dental insurance
Quick Apply
Economic Development & Housing Manager
City of Bell —Bell, CA
- $105,000 - $120,000 a year
- Full-time
- Customer service
- 5 years
- Word processing
- Health insurance
- Dental insurance
Quick Apply
Head of Brand
Our Place —Los Angeles, CA
- $150,000 - $200,000 a year
- Full-time
- Hybrid work
- Research
- Office
- In-person
- Store discount
- Health insurance
Stylist
Fendi —Los Angeles, CA
- $40 an hour
- Full-time
- 5 years
- Merchandising
- Mid-level
- Paid holidays
- Disability insurance
13d
Affordable Housing Community Manager
Asset Living —Los Angeles, CA
- $29 an hour
- On call
- Mid-level
- High school diploma or GED
- Bachelor's degree
- Paid holidays
- Disability insurance
Quick Apply
Governance, Risk & Compliance (GRC) Manager
Northwood Space —Los Angeles, CA
- Full-time
- AWS
- Senior level
12d
Case Manager - Master's Degree
STG International, Inc. —Los Angeles, CA
- From $30 an hour
- Addiction Medicine
- Mid-level
- Driver's License
- Health insurance
- Dental insurance
Quick Apply
RBT
California Behavioral Care —Los Angeles, CA
- $23 - $25 an hour
- Part-time
- Bilingual
- Background check
- CPR Certification
Quick Apply
13d
Project/Administrative III
J. Paul Getty Trust, The —Los Angeles, CA
- $28.05 - $35.76 an hour
- Full-time
- Hybrid work
- Microsoft Outlook
- Mid-level
- Office
- Paid holidays
- Health insurance
Product Manager, New Business
Feit Electric —Pico Rivera, CA
- $120,000 - $150,000 a year
- Email
- Mid-level
- Office
- Residential
- Health insurance
- Dental insurance
7d
Production Coordinator
Company3 —Hollywood, CA
- $24 - $26 an hour
- Overtime
- Mid-level
- Office
- Travel
- Health insurance
- Paid time off
Head of Merchandising
JustFab —El Segundo, CA
- $150,000 - $200,000 a year
- Full-time
- Marketing
- Merchandising
- English
Director of Energy and Environmental Services
PACE —Los Angeles, CA
- $160,000 - $200,000 a year
- Online Application
- 5 years
- Ability to sit for extended periods
- Organizational skills
- Paid holidays
- Health insurance
QIDP (Quality Intellectual Disability Professional)
Bloomfield West —Lynwood, CA
- $28 - $32 an hour
- Full-time
- Psychiatry
- Mid-level
- Bachelor's degree
Quick Apply
5d
Global Head of Sales Apparel
blackcrows —Los Angeles, CA
- Full-time
- Hybrid work
- Inventory management
- English
- 8 years
- Disability insurance
- Dental insurance
OPTICAL SALES ASSOCIATE (ALL GENDERS) | BEVERLY HILLS, LOS ANGELES
MYKITA GmbH —Los Angeles, CA
- Weekends as needed
- Customer service
- 1 year
- Communication skills
- Health insurance
- Paid time off
Campaign Organizer
Sierra Club —Los Angeles, CA
- $68,500 - $70,000 a year
- Full-time
- Remote
- Google Workspace
- Mid-level
- Organizational skills
- Health insurance
- Dental insurance
Quick Apply
7d

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Clinical Research Coordinator II – Head & Neck (Hybrid Role)

CEDARS-SINAI -
Beverly Hills, CA

Apply Now

Job Details

Full-time

Qualifications

High school diploma or GED

Full Job Description

Job Description

The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents information at regular research staff meetings. May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying new research opportunities. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).

This role follows a hybrid work schedule; however, we can only consider applicants who will be able to commute to our Los Angeles work location a few times per week. If hired you must reside in the commutable area.

Primary Duties and Responsibilities

Independent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process.
Schedules patients for research visits and procedures.
In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug.
Maintains accurate source documents related to all research procedures.
Responsible for accurate and timely data collection, documentation, entry, and reporting including timely response to sponsor queries.
Schedules and participates in monitoring and auditing activities.
Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information; present this information at regular research staff meetings.
Notifies direct supervisor about concerns regarding data quality and study conduct.
Works closely with a regulatory coordinator or directly with the Institutional Review Board (IRB) to submit Adverse Events, Serious Adverse Events, protocol deviations, and Safety Letters in accordance with local and federal guidelines.
May perform other regulatory / Institutional Review Board duties, budgeting duties, and assisting with patient research billing and reconciliation.
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA and local Institutional Review Board.
Maintains research practices using Good Clinical Practice (GCP) guidelines.
Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
May coordinate training and education of other personnel.
May participate in centralized activities such as auditing, Standard Operating Procedure development, etc.
May plan and coordinate strategies for increasing patient enrollment, and/or improving clinical research efficiency. Primary Duties and Responsibilities
May identify quality and performance improvement opportunities and collaborate with staff in the development of action plans to improve quality.
May identify new research opportunities and present to investigators
Participates in required training and education programs.

Department / Unit Responsibilities

Verifies specimen identification and assesses the appropriateness of test orders and specimen quality by recognizing factors that may affect procedures or results; takes corrective action when necessary.
Ensures accurate patient and specimen identification through strict adherence to established procedures; labels all samples accurately and completely.
Reports test results to the appropriate individuals and maintains strict professional discretion with all patient information.

Neuroscience

Transports research medications in accordance with established protocols.
Performs research-related assessments and administers study questionnaires.
Assists with prescreening of potential research participants for various clinical trials.
Participates in research meetings and monthly sponsor conference calls for study updates.
Maintains well-organized paper and electronic research files.
Conducts all data collection and data entry activities for department clinical trials.
Assists in preparing manuscripts, letters, and other research documents as needed.
Responds to sponsor inquiries regarding protocol start-up and participant recruitment activities.
Conducts literature reviews to support research activities.

Hepatology Transplant Research

Assists with budget development and negotiation in collaboration with CTAO and study sponsors, ensuring full compliance with all CSMC policies.
May support the training and education of other personnel as needed.

Qualifications

Job Minimum Qualifications:

High School Diploma/GED required. Bachelors Degree preferred.
2 years Clinical research related experience required.

Apply Now

Refine Your Search

head collection development jobs in los angeles, ca

Clinical Research Coordinator II – Head & Neck (Hybrid Role)

Facilities Coordinator

Service Area Supervisor

CSPP Program Specialist

Economic Development & Housing Manager

Head of Brand

Stylist

Affordable Housing Community Manager

Governance, Risk & Compliance (GRC) Manager

Case Manager - Master's Degree

RBT

Project/Administrative III

Product Manager, New Business

Production Coordinator

Head of Merchandising

Director of Energy and Environmental Services

QIDP (Quality Intellectual Disability Professional)

Global Head of Sales Apparel

OPTICAL SALES ASSOCIATE (ALL GENDERS) | BEVERLY HILLS, LOS ANGELES

Campaign Organizer

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