Top 180 Clinical trial assistant Jobs in Stanford, Ca

Assistant Clinical Research Coordinator
Stanford University —Redwood City, CA
- Extended hours
- Hybrid work
- Vital signs
- Office
- Administrative experience
Assistant Clinical Research Coordinator (50% FTE)
Stanford University —Stanford, CA
- Part-time
- Hybrid work
- Experience working with individuals with developmental disabilities
- Vital signs
- Writing skills
2d
Clinical Trial Assistant
Intuitive Surgical —Sunnyvale, CA
- $34 - $46 an hour
- Day shift
- Surgery
- Mid-level
- Office
Assistant Clinical Research Coordinator, Emergency Medicine (Hybrid Opportunity)
Stanford University —Stanford, CA
- Full-time
- Hybrid work
- Vital signs
- Addiction Medicine
- University
11d
Clinical Trial Assistant
Sagimet Biosciences —Foster City, CA
- Hybrid work
- Mid-level
- Bachelor's degree
- Organizational skills
Clinical Research Coordinator Associate
Stanford University —Redwood City, CA
- Full-time
- Hybrid work
- Psychiatry
- Mid-level
- Databases
Clinical Research Assistant – Health Educator
PAVIR —Menlo Park, CA
- From $31.25 an hour
- Temporary
- Background check
- Master's degree
- Bachelor's degree
- Wellness program
- Commuter assistance
Quick Apply
8h
Assistant Clinical Research Coordinator (12-Month Fixed-Term)
Stanford University —Stanford, CA
- Full-time
- Vital signs
- Inpatient
- Outpatient experience
11d
Clinical Trial Associate
Karius —Redwood City, CA
- $60,842 - $91,264 a year
- Full-time
- Remote
- Google Workspace
- Mid-level
- Bachelor's degree
Quick Apply
4d
Clinical Research Coordinator I – The Nallamshetty Lab
PAVIR —Palo Alto, CA
- $35.19 - $45.67 an hour
- Full-time
- Background check
- HIPAA
- Laboratory experience
- Wellness program
- Commuter assistance
Quick Apply
3d
Neuroimaging Research Assistant
Stanford University —Stanford, CA
- $38.55 - $46.68 an hour
- Extended hours
- English
- Mid-level
- Databases
Clinical Research Coordinator II
Stanford University —Stanford, CA
- $86,248 - $100,158 a year
- Extended hours
- Hybrid work
- HIPAA
- Mid-level
- University
Clinical Research Coordinator Associate (2 Vacancies) (On-Site)
Stanford University —Stanford, CA
- Full-time
- HIPAA
- Mid-level
- Databases
Research Specialist
RDE Logistics —Palo Alto, CA
- $37 - $44 an hour
- Full-time
- Mid-level
- Databases
- In-person
Quick Apply
Social Science Research Coordinator
Stanford University —Stanford, CA
- $30 - $40 an hour
- Full-time
- Hybrid work
- Management
- Computer literacy
- Mid-level
3d
Cancer Clinical Research Coordinator Associate - GynOncology(Hybrid)
Stanford University —Stanford, CA
- Extended hours
- Hybrid work
- Databases
- University
- Bachelor's degree
7d
Clinical Research Associate II
Imperative Care —Campbell, CA
- $101,000 - $106,000 a year
- Full-time
- Mid-level
- Office
- Bachelor's degree
- Health insurance
- 401(k)
Clinical Trials Regulatory Specialist 1
Stanford University —Stanford, CA
- Full-time
- Hybrid work
- Customer service
- Microsoft Office
- 3 years
4d
FSP CRA II - Alzheimer's Experience - US West
Thermo Fisher Scientific —California
- $88,600 - $132,000 a year
- Full-time
- RN License
- Writing skills
- English
- Commuter assistance
- Paid parental leave
Clinical Research Associate II
Corcept Therapeutics —Redwood City, CA
- $129,400 - $152,300 a year
- Bachelor of Science
- Mid-level
- 3 years
Quick Apply

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Assistant Clinical Research Coordinator

Stanford University -
Redwood City, CA

Apply Now

Job Details

Full-time

Qualifications

Biology
Bachelor's degree in biological science
Vital signs
Regulatory documents
Safety protocol adherence
EKG
AI tools proficiency
Project coordination
Phlebotomy specimen handling
Administrative experience
Social Sciences
Research project coordination
Medical administrative support
Bachelor's degree
Non-CDL Class C
Informed consent procedures implementation
Compliance documentation
Medical record abstraction
Desktop applications
Organizational skills
Telephone interviewing
Biological sampling
Implementing research protocols
Patient recruitment
Clerical experience
1 year
Research participation
Data accuracy checks
Clinical research documentation
Ordering supplies

Full Job Description

Stanford University’s Department of Dermatology is seeking an Assistant Clinical Research Coordinator (ACRC) to perform administrative support duties related to the collection of clinical data and the coordination of clinical studies. This position is hybrid and requires at least 3 days in the office a week at the Redwood City Campus. In this role, the ACRC will work under the supervision of the principal investigator and the clinical research manager.

Interested candidates, please apply with your resume and a cover letter.

DESIRED QUALIFICATIONS:

A Bachelor’s degree with an educational background in medicine and/or scientific field (biological sciences, social sciences, etc.)
Proven ability to work independently and take ownership of a project.
Proven ability to work collaboratively and cooperatively in a team environment.
Ability to work effectively in a fast-paced environment and balance multiple projects and timelines at one time.
Strong oral and written communication skills.
Detail-oriented with excellent organizational skills.

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.

* - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.

WORKING CONDITIONS:

Position may at times require the employee to work with or be in areas where hazardous materials and/or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious diseases and infections.

WORK STANDARDS:

Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, http://adminguide.stanford.edu .

Core Duties :

Schedule and/or call subjects for appointments; contact participants with reminders or other requirements.
Prepare, distribute, and process questionnaires.
Perform clerical duties in the preparation of regulatory documents. Maintain all forms and documents, including consent forms and master subject logs. File all appropriate correspondence.
Assist with the screening, recruiting, and obtaining consent of study participants. Review medical records and/or perform telephone or in-person interviews to gather data, as needed.
Administer standard study questionnaires and tests, score test measurements and questionnaires, and code data for computer entry. Perform quantitative review of forms, tests, and other measurements for completeness and accuracy.
Extract data from source documents for research studies as directed. Collect data and complete case report forms.
Perform basic measurements and tests on patients according to protocol, such as obtaining vital signs and performing phlebotomy and EKG, after appropriate training/certification. Collect study specimens according to protocol.
Prepare, process, and ship specimens/samples accurately under well-defined requirements.
Order and maintain equipment and supplies.

Minimum Education and Experience

Two-year college degree and one year of relevant experience or an equivalent combination of experience, education, and training.

Knowledge, Skills and Abilities :

General knowledge of medical terminology.

Certificates and Licenses Required

Working toward certification(s) to perform basic patient measurements and tests, such as phlebotomy and EKG.

Must possess and maintain a valid California non-commercial Class C Driver's License, if applicable.

Apply Now

Refine Your Search

clinical trial assistant jobs in stanford, ca

Assistant Clinical Research Coordinator

Assistant Clinical Research Coordinator (50% FTE)

Clinical Trial Assistant

Assistant Clinical Research Coordinator, Emergency Medicine (Hybrid Opportunity)

Clinical Trial Assistant

Clinical Research Coordinator Associate

Clinical Research Assistant – Health Educator

Assistant Clinical Research Coordinator (12-Month Fixed-Term)

Clinical Trial Associate

Clinical Research Coordinator I – The Nallamshetty Lab

Neuroimaging Research Assistant

Clinical Research Coordinator II

Clinical Research Coordinator Associate (2 Vacancies) (On-Site)

Research Specialist

Social Science Research Coordinator

Cancer Clinical Research Coordinator Associate - GynOncology(Hybrid)

Clinical Research Associate II

Clinical Trials Regulatory Specialist 1

FSP CRA II - Alzheimer's Experience - US West

Clinical Research Associate II

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