Top 18 Cra Jobs in Redwood City, Ca

Clinical Trial Assistant
Intuitive Surgical —Sunnyvale, CA
- $34 - $46 an hour
- Day shift
- Surgery
- Mid-level
- Office
Clinical Research Associate II
Corcept Therapeutics —Redwood City, CA
- $129,400 - $152,300 a year
- Bachelor of Science
- Mid-level
- 3 years
Quick Apply
On-site Clinical Research Associate
Protagonist Therapeutics —Newark, CA
- $125,000 - $135,000 a year
- English
- Mid-level
- Office
Quick Apply
Clinical Research Coordinator
viva —Palo Alto, CA
- $46.72 - $51.72 an hour
- Full-time
- HIPAA
- Mid-level
- Bachelor's degree
Clinical Research Associate II
Abbott Laboratories —Alameda, CA
- $81,500 - $141,300 a year
- Full-time
- Up to 50% travel
- Bachelor of Science
- Writing skills
- Health insurance
- Tuition reimbursement
CRA 2, Early Clinical Development
IQVIA —San Francisco, CA
- $90,200 - $150,400 a year
- Full-time
- Mid-level
- Bachelor's degree
- Travel
Senior Clinical Research Associate
Protagonist Therapeutics —Newark, CA
- $135,000 - $150,000 a year
- English
- Office
- Bachelor's degree
Quick Apply
Development Business Operations Associate
MEDVACON Life Sciences —Foster City, CA
- Contract
- Hybrid work
- PMP
- Bachelor of Science
- Mid-level
Quick Apply
Director of Clinical Studies
Pendulum™ —San Francisco, CA
- $223,200 - $248,000 a year
- Full-time
- Hybrid work
- Nursing
- 3 years
- Bachelor's degree
- Commuter assistance
- Disability insurance
Quick Apply
Clinical Trial Manager (CTM)
Corcept Therapeutics —Redwood City, CA
- $156,600 - $184,300 a year
- Hybrid work
- Nursing
- 6 years
- Bachelor of Science
Quick Apply
Senior Manager Clinical Affairs
Intuitive Surgical —Sunnyvale, CA
- $157,800 - $278,400 a year
- Day shift
- Medicine
- Surgery
- 5 years
CLIN RSCH SUPV 1
University of California San Francisco —San Francisco, CA
- 3 years
- Analysis skills
- University
Subject Mater Expert, Clinical Trials
HCT Healthcare Transformation —San Jose, CA
- $150,000 - $160,000 a year
- Nursing
- RN License
- Hospital
Senior Global Clinical Study Manager
IQVIA —San Francisco, CA
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Mentoring
- Work from home

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On-site Clinical Research Associate
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Clinical Trial Assistant
Intuitive Surgical —Sunnyvale, CA
Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export…
$34 - $46 an hour

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Clinical Trial Assistant

Intuitive Surgical -
Sunnyvale, CA

Apply Now

Job Details

$34 - $46 an hour

Qualifications

High school diploma or GED
Video conferences (communication methods)

Full Job Description

Sunnyvale, CA, United States
Not Remote
Clinical & Medical Affairs
JOB217293

Company Description

It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive. As a global leader in robotic-assisted surgery and minimally invasive care, our technologies—like the da Vinci surgical system and Ion—have transformed how care is delivered for millions of patients worldwide.

We’re a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world.

The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful—because every improvement we make has the potential to change a life.

If you’re ready to contribute to something bigger than yourself and help transform the future of healthcare, you’ll find your purpose here.

Job Description

Primary Function of Position:

The Clinical Trial Assistant will play a key role to provide operational support to coordinate the conduct and management of clinical studies to ensure compliance with Intuitive standard operating procedures, Good Clinical Practices (GCP), good documentation practices, and applicable regulations. The ideal candidate will have good understanding of clinical trials regulatory requirements. This position is based at the Intuitive Surgical Headquarters in Sunnyvale, California.

Roles & Responsibilities:

Coordinate and manage the ordering, shipping, labeling and tracking of study supplies (including investigational products) with limited supervision
Establish, organize and maintain trial master file and clinical trial management system to ensure regulatory and protocol compliance including maintenance of study essential documentation (e.g., correspondence, CRFs, study approval documents, curriculum vita, etc…), trip reports, site contact documentation, monthly status reports (e.g., enrollment, adverse events, budget, etc.)
Contribute to operational excellence and continuous improvement
Maintain, track and facilitate routing for approval and signature of clinical study documents including protocols, case report forms, Informed consents, Clinical trial agreements, non-disclosure agreements, etc
Create purchase requests and process invoices
Support clinical study manager with study budget tracking and payments of clinical sites and vendors
Prepare and ship site binders and patient binders as necessary
Contribute to creating clinical study informational materials such as newsletters, recruitment materials, etc.
Collaborate with Clinical Study Managers (CSM) to develop clinical study informational materials such as newsletters, recruitment materials, etc
Collaborate with Clinical Research Associates (CRA), Clinical Study Managers (CSM) and Clinical Managers to support study execution
Provide administrative support to coordinate, schedule and plan study and investigators meetings, teleconferences, distributing agendas and meeting minutes

Qualifications

Skills, Experience, Education, & Training:

Excellent communication, organization and interpersonal skills with strong attention to detail
Strong ability to organize, prioritize and manage multiple priorities
Prior experience in medical device clinical trials, regulatory support, clinical project coordination
Proficient in MS Office suite, Adobe, video and web conferencing solutions
Clinically savvy & good knowledge of basic medical terminology preferred
Possess working knowledge of Good Clinical Practice as detailed in 21CFR and ISO 14155, and regulation such as 21 CFR Part 812
Minimum of 2-4 years of related experience in clinical research with high school diploma or secondary education or equivalent
Minimum Bachelor’s degree is a plus
Research/clinical trial management certification/ education is a plus
Able to travel up to 10%
We provide market-competitive compensation packages, inclusive of base pay, incentives, benefits and equity, and the anticipated pay rate for this position is $70,000 to $94,800
It would not be typical for someone to be hired at the top end of range for the role, as actual pay will be determined based on several factors, including location, skills, and experience level

Additional Information

Due to the nature of our business and the role, please note that Intuitive and/or your customer(s) may require that you show current proof of vaccination against certain diseases including COVID-19. Details can vary by role.

Intuitive is an Equal Opportunity Employer. We provide equal employment opportunities to all qualified applicants and employees, and prohibit discrimination and harassment of any type, without regard to race, sex, pregnancy, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, genetic information or any other status protected under federal, state, or local applicable laws.

Mandatory Notices

U.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status.

Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government’s licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan (“TCP”) (note: typically adds 2 weeks to the hiring process).

For any Intuitive role subject to export controls, final offers are contingent upon obtaining an approved export license and/or an executed TCP prior to the prospective employee’s start date, which may or may not be flexible, and within a timeframe that does not unreasonably impede the hiring need. If applicable, candidates will be notified and instructed on any requirements for these purposes.

We will consider for employment qualified applicants with arrest and conviction records in accordance with fair chance laws.

Preference will be given to qualified candidates who do not reside, or plan to reside, in Alabama, Arkansas, Delaware, Florida, Indiana, Iowa, Louisiana, Maryland, Mississippi, Missouri, Oklahoma, Pennsylvania, South Carolina, or Tennessee.

This position may be filled at a different job level than listed here depending on
business need and/or on the selected candidate’s experience, knowledge and skills.
Compensation will be based primarily on the job level at which the role is filled and the
candidate’s qualifications, consistent with applicable law.

We provide market-competitive compensation packages, inclusive of base pay, incentives, benefits, and equity. It would not be typical for someone to be hired at the top end of range for the role, as actual pay will be determined based on several factors, including experience, skills, and qualifications. The target compensation ranges are listed.

Base Compensation Range Region 1: $40 USD - $54 USD
Base Compensation Range Region 2: $34 USD - $46 USD
Shift: Day
Workplace Type: Onsite - This job is fully onsite.

Apply Now

Refine Your Search

cra jobs in redwood city, ca

Clinical Trial Assistant

Clinical Research Associate II

On-site Clinical Research Associate

Clinical Research Coordinator

Clinical Research Associate II

CRA 2, Early Clinical Development

Senior Clinical Research Associate

Development Business Operations Associate

Director of Clinical Studies

Clinical Trial Manager (CTM)

Senior Manager Clinical Affairs

CLIN RSCH SUPV 1

Subject Mater Expert, Clinical Trials

Senior Global Clinical Study Manager

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