Top 121 Clinical data coordinator Jobs in Thousand Oaks Ca

Clinical Research Coordinator
SCLA Management —Thousand Oaks, CA
- $50,000 - $60,000 a year
- Full-time
- Vital signs
- Computer literacy
- Mid-level
- Paid time off
Quick Apply
2d
Clinical Data Review Coordinator
UCLA Health —Santa Monica, CA
- $95,400 - $208,300 a year
- Nursing
- RN License
- Mid-level
Assistant Clinical Research Coordinator - Pediatrics
UCLA Health —Los Angeles, CA
- $30.74 - $49.46 an hour
- Hybrid work
- Word processing
- Computer literacy
- Neurology
8d
Healthcare Coordinator
PDS Health —Thousand Oaks, CA
- $18.00 - $25.50 an hour
- Part-time
- Dental office
- Computer literacy
- Local
- Health insurance
- Dental insurance
Clinical Research Coordinator
UCLA Health —Los Angeles, CA
- $38.19 - $61.45 an hour
- Word processing
- Computer literacy
- Mid-level
9h
Clinical Research Coordinator - Neurology
UCLA Health —Los Angeles, CA
- $38.19 - $61.45 an hour
- Word processing
- Computer literacy
- Mid-level
5d
Assistant Clinical Research Coordinator - Urology
UCLA Health —Los Angeles, CA
- $30.74 - $49.46 an hour
- Word processing
- Computer literacy
- Data entry
5d
Clinical Research Coordinator - Radiological Sciences
UCLA Health —Los Angeles, CA
- $38.19 - $61.45 an hour
- Word processing
- Computer literacy
- Mid-level
1d
Clinical Research Coordinator
California Retina Consultants —Oxnard, CA
- $25.50 - $31.50 an hour
- Full-time
- Background check
- Anatomy knowledge
- Pass drug screening
- Paid holidays
- Dental insurance
Quick Apply
Assistant Clinical Research Coordinator – Pediatrics
UCLA Health —Los Angeles, CA
- $30.74 - $49.46 an hour
- Weekends as needed
- Spanish
- Computer literacy
- English
8d
Physician needed for Clinical Research MD/DO ONLY
Confidential —West Hills, CA
- $100 - $150 an hour
- Part-time
- CPR Certification
- Medicine
- Patient monitoring
Quick Apply
7d
Registered Nurse Team Lead -Every other Weekend-
Livingston Memorial VNA —Ventura, CA
- $45 - $50 an hour
- Weekends as needed
- Microsoft Word
- Microsoft Excel
- RN License
- Paid training
- Paid holidays
VASH Lead Service Coordinator III
Step Up On Second, INC., —Los Angeles, CA
- $78,000 - $85,000 a year
- Full-time
- Background check
- LMFT
- Master of Social Work
- 403(b) matching
- Paid holidays
Quick Apply
Lead Service Coordinator III, VASH
Step Up on second, INC —Los Angeles, CA
- $78,000 - $85,000 a year
- Full-time
- Hybrid work
- Background check
- LMFT
- Master of Social Work
- 403(b) matching
- Paid holidays
Quick Apply
VASH Assistant Program Manager
Step Up On Second, INC., —Los Angeles, CA
- $86,000 - $92,000 a year
- Full-time
- Background check
- LMFT
- Master of Social Work
- 403(b) matching
- Paid holidays
Quick Apply
MDS Coordinator- RN/LVN
Glenwood Care Center —Oxnard, CA
- $36 - $55 an hour
- Full-time
- Background check
- Nursing
- Skilled nursing facility
Quick Apply
Case Manager Home Health
Alliance Home Health Group —Woodland Hills, CA
- $35 - $38 an hour
- Overtime
- LVN
- RN License
- Mid-level
- Health insurance
- 401(k)
Quick Apply
Clinical Supervisor (BCBA)
Center for Autism and Related Disorders —Northridge, CA
- $76,000 - $116,000 a year
- Full-time
- Microsoft Outlook
- Current TB test
- HIPAA
- Paid training
- Relocation assistance
Quick Apply
Oncology Clinical Research Coordinator, RN
START Center for Cancer Research —Los Angeles, CA
- $55 - $70 an hour
- Monday to Friday
- Nursing
- RN License
- Mid-level
- Health savings account
- Paid holidays
Quick Apply
Data Coordinator
START Center for Cancer Research —Los Angeles, CA
- $25 - $35 an hour
- Monday to Friday
- Mid-level
- Office
- High school diploma or GED
- Health savings account
- Paid holidays
Quick Apply
2d

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Clinical Research Coordinator

SCLA Management
Thousand Oaks, CA

Quick Apply

Job Details

Full-time
$50,000 - $60,000 a year
2 days ago

Benefits

Paid time off

Qualifications

Computer operation
Vital signs
Computer literacy
In-person customer service
Patient demographics
Patient weighing scales
Care documentation
Phlebotomy specimen handling
Mid-level
ECG equipment
Research project coordination
Clinical data entry
Packaging
Informed consent procedures implementation
Compliance documentation
Patient care
Quality control operations
Clinical trial standard operating procedures
Implementing research protocols
Health status assessment
Clinical quality assurance standards
Research participation
Patient education
Clinical trial support in drug product development
Leadership
Standard operating procedures (SOPs)
Medical terminology
Communication skills
Project stakeholder communication
Quality data entry

Full Job Description

The Clinical Research Coordinator (CRC) is responsible for managing clinical trial performance and ensuring the conduct of their clinical trials. The CRC plans, coordinates, evaluates, and manages the care of both the participants and of the data for their assigned trials. The CRC follows study specific protocol guidelines and communicates and interacts with Investigators, clinic staff, CROs and Sponsors to effectively perform clinical research and coordinate research activities. All duties carried out by the CRC are done in accordance with company policies, Standard Operating Procedures (SOP), and Good Clinical Practice (GCP), as well as all applicable local, state and federal regulations.

Primary Responsibilities

Coordinate clinical trials conducted by a supervising Principal Investigator in accordance with FDA, GCP and protocol guidelines.
Identify potential problems or inconsistencies and take action as appropriate.
Collect initial subject health and demographic information by interviewing subjects and accessing other appropriate sources.
Review subject comprehensive medical documentation to determine protocol eligibility under the supervision of the Principal Investigator.
Ensure a flow of communication including telephone conferences between subject, study staff, referral sources and recruitment team, Sponsor and/or CRO, Monitor(s) and Auditors, if applicable.
Perform clinical tasks including, but not limited to: vital signs, height and weight, ECG, phlebotomy, specimen processing and packaging.
Maintain timely internal source documentation as well as sponsor-required information.
Maintain timely EDC data entry and query resolution.
Maintain timely internal study tracking metrics of patient visits and study information.
Complete Verification of subjects before consenting.
Dispense and maintain accurate records of investigational and study product.
Educate subject and family members regarding specific studies and clinical drug trials in general.
Complete all monitor and sponsor queries in a timely manner.
Perform Quality Control (QC) checks on all trials per company SOP and interface with QA Director as needed

Recruitment Responsibilities

Participate in recruitment planning meetings prior to study start
Communicate all updates to Sponsor and recruitment team
Maintain weekly communication with recruitment team in order to maximize recruitment in all enrolling trials

Secondary Responsibilities

Maintains Quality and Accuracy Standards by

Reading, understanding and adhering to organizational Standard Operating Procedures (SOP)
Assisting in establishing and enforcing departmental standards
Contributes to team effort by
Working with practice staff to resolve issues
Exploring new opportunities to add value to the organization and departmental processes
Helping others at the practice to achieve study goals
Performing other duties as assigned
Support the organization’s mission and goals
Maintains Technical and Industry Knowledge by
Attending and participating in Sponsor investigator meetings, recruitment meetings, and trainings

Additional skill set:

Strong motivational skills and abilities
Strong interpersonal and communication skills, both verbal and written
Strong organizational and leadership skills
Goal oriented
Ability to maintain a professional and positive attitude
Detail oriented
Strong critical thinking skills
Strong ability to multi-task
Strong computer skills
Ability to support and demonstrate the mission and goals of the company
Excellent interpersonal and customer service skills
Knowledge of medical terminology and clinical practices

Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.

Report to duty at physical locations other than the primary assigned location(s) on an as-needed basis.

Experience

CRC in clinical research or relevant clinical role preferred but not required

Job Type: Full-time

Pay: $50,000.00 - $60,000.00 per year

Benefits:

Paid time off

Work Location: In person

Quick Apply

Refine Your Search

clinical data coordinator jobs in thousand oaks ca

Clinical Research Coordinator

Clinical Data Review Coordinator

Assistant Clinical Research Coordinator - Pediatrics

Healthcare Coordinator

Clinical Research Coordinator

Clinical Research Coordinator - Neurology

Assistant Clinical Research Coordinator - Urology

Clinical Research Coordinator - Radiological Sciences

Clinical Research Coordinator

Assistant Clinical Research Coordinator – Pediatrics

Physician needed for Clinical Research MD/DO ONLY

Registered Nurse Team Lead -Every other Weekend-

VASH Lead Service Coordinator III

Lead Service Coordinator III, VASH

VASH Assistant Program Manager

MDS Coordinator- RN/LVN

Case Manager Home Health

Clinical Supervisor (BCBA)

Oncology Clinical Research Coordinator, RN

Data Coordinator

I want to receive the latest job alert for clinical data coordinator in thousand oaks ca

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