Top 4 Sleep lab Jobs in Redwood City, Ca

Clinical Research Coordinator Associate
Stanford University —Stanford, CA
- Full-time
- Hybrid work
- Psychiatry
- Bachelor of Science
- Mid-level
11d
Polysomnographic Technologist II, Sleep Lab
Sutter Health —Fremont, CA
- $50.65 - $70.90 an hour
- Weekends as needed
- Writing skills
- BLS Certification
- Data analysis skills
Research Associate
Eight Sleep —San Francisco, CA
- $70,000 - $100,000 a year
- Weekends as needed
- Computer Science
- HIPAA
- Mid-level
Clinical Research Manager 1
Stanford University —Stanford, CA
- Full-time
- Management
- 5 years
- HIPAA
2d

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Sleep Technician II
Lucile Packard Children's Hospital Stanford —Mountain View, CA
Knowledge of new technologies (in specific field) and maintain and stay abreast of updates and changes. Any combination of education and experience that would…
$47.85 - $54.26 an hour
6d
Polysomnographic Technologist II - Limited Term
Sutter Health —Redwood City, CA
Basic computer skills are essential for record analysis. Base pay is only one component of Sutter Health’s comprehensive total rewards program.
$50.65 - $70.90 an hour
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Polysomnography Technician Ambulatory Services | Outpatient Care Powell Sleep Lab
The Ohio State University Wexner Medical Center —Powell, OH
The laboratory is the diagnostic area of the Division of Pulmonary and Critical Care. It evaluates all patients suspected of having sleep disorders.
Research Associate- Pulmonary Critical Care and Sleep
The Ohio State University Wexner Medical Center —Columbus, OH
Research Associate who participates in planning, design, execution, and management of research projects in a foundational (basic) biological/health science…
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Clinical Research Coordinator Associate

Stanford University -
Stanford, CA

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Job Details

Full-time
11 days ago

Qualifications

Managing scientific research projects
Managing healthcare project budgets
Project documentation
Bachelor of Science
Filing
Mid-level
Patient safety
Databases
Clinical audit and monitoring
Schedule management
Bachelor's degree
Data management
Project monitoring
Driving
Desktop applications
Research compliance clinical trial records management
Laboratory specimen handling
Clinical trial patient safety management
Implementing research protocols
Regulatory submission editing and review
Patient recruitment
CCRP
Communication with regulatory authorities for clinical trials
Managing projects
Productivity software
Research participation
Patient data collection
Research budget management
Managing patient records
Ethical review application preparation

Full Job Description

The Division of Sleep Medicine in the Department of Psychiatry & Behavioral Sciences at Stanford University is seeking a fulltime position 100%FTE Clinical Research Coordinator Associate. The Clinical Research Coordinator Associate will work closely with the physicians and staff at the Stanford Sleep Medicine Center to ensure that patients are properly enrolled in the research study, receive complete information about their tests and procedures, have their data from their tests and outcome measures properly collected, and are provided access to their results. They will coordinate moderately complex aspects of one or more clinical studies and work under close direction of the Division Chief.

DESIRED QUALIFICATIONS:

BA/BS degree in a related science field
Prior experience with project management

PHYSICAL REQUIREMENTS*:

Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.
Ability to drive day or night, if applicable.

WORKING CONDITIONS:

Occasional evening and weekend hours.

Core Duties :

Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through closeout.
Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.
Coordinate collection of study specimens and processing.
Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure Institutional Review Board renewals are completed.
Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.

Minimum Education and Experience

Two-year college degree and two years related work experience or a bachelor’s degree in a related field or an equivalent combination of related education and relevant experience.

Knowledge, Skills and Abilities :

Strong interpersonal skills.
Proficiency with Microsoft Office.

Certificates and Licenses Required

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.

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sleep lab jobs in redwood city, ca

Clinical Research Coordinator Associate

Polysomnographic Technologist II, Sleep Lab

Research Associate

Clinical Research Manager 1

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