Top 149 Clinical research associate Jobs in Fremont Ca

Clinical Research Associate
Protagonist Therapeutics —Newark, CA
- $125,000 - $135,000 a year
- English
- Mid-level
- Bachelor's degree
Quick Apply
Clinical Data Manager - II
Apollo Professional Solutions, Inc. —South San Francisco, CA
- $78 - $85 an hour
- Contract
- Hybrid work
- 5 years
- Office
- Continuous improvement
- Dental insurance
- 401(k)
Quick Apply
1d
Senior Clinical Research Associate
Protagonist Therapeutics —Newark, CA
- $135,000 - $150,000 a year
- English
- Mid-level
- Bachelor's degree
Quick Apply
In House Clinical Research Associate
Ardelyx —Newark, CA
- $99,000 - $121,000 a year
- Full-time
- Mid-level
- Analysis skills
- Bachelor's degree
- Paid parental leave
- Paid holidays
Neuroimaging Research Assistant
Stanford University —Stanford, CA
- $38.55 - $46.68 an hour
- Extended hours
- English
- Mid-level
- Databases
Clinical Research Coordinator Associate
Stanford University —Stanford, CA
- $34.79 - $43.68 an hour
- Full-time
- Hybrid work
- Mid-level
- Databases
- University
Clinical Research Coordinator
Stanford University —Stanford, CA
- $86,248 - $100,158 a year
- Extended hours
- HIPAA
- Mid-level
- University
Clinical Research Coordinator II
Stanford University —Stanford, CA
- $86,248 - $100,158 a year
- Extended hours
- HIPAA
- Mid-level
- University
Clinical Data Manager
CliniOps —Fremont, CA
- Mid-level
- Windows
- Analysis skills
Clinical Research Coordinator 2
Stanford University —Stanford, CA
- $86,248 - $100,158 a year
- Extended hours
- HIPAA
- Mid-level
- Databases
Senior Clinical Research Associate
Corcept Therapeutics —Redwood City, CA
- $149,000 - $170,000 a year
- Hybrid work
- Nursing
- Bachelor of Science
- Office
Clinical Trial Manager - Contractor
Arcus Biosciences —Hayward, CA
- Contract
- Office
- Bachelor's degree
- Travel
Associate Director, Clinical Operations
Protagonist Therapeutics —Newark, CA
- $185,000 - $205,000 a year
- 5 years
- English
- Bachelor's degree
Quick Apply
Clinical Research Associate II
Corcept Therapeutics —Redwood City, CA
- $129,400 - $152,300 a year
- Bachelor of Science
- Mid-level
- 3 years
Quick Apply
7d
Clinical Research Manager
Stanford University —Stanford, CA
- $124,521 - $153,615 a year
- Extended hours
- 5 years
- HIPAA
- Master's degree
Clinical Research Associate
Alameda Health System —Oakland, CA
- $49.48 - $60.16 an hour
- Hospital
- BLS Certification
- Mid-level
Quick Apply
Clinical Research Coordinator – Cooperative Studies Program
PAVIR —Palo Alto, CA
- From $35.04 an hour
- Full-time
- Hybrid work
- Background check
- HIPAA
- Mid-level
- Wellness program
- Commuter assistance
Quick Apply
Clinical Research Assistant – Exploratory Therapeutics Laboratory
PAVIR —Palo Alto, CA
- From $34 an hour
- Full-time
- Microsoft Word
- Background check
- Mid-level
- Wellness program
- Commuter assistance
Quick Apply
Clinical Research Data Analyst II – Chronic Liver Diseases
PAVIR —Palo Alto, CA
- $97,407.20 - $100,000.00 a year
- Full-time
- Hybrid work
- Background check
- HIPAA
- Mid-level
- Wellness program
- Commuter assistance
Quick Apply
Clinical Project Manager - Pleasanton, CA
Calyxo —Pleasanton, CA
- $140,000 - $150,000 a year
- 7 years
- Up to 50% travel
- Bachelor of Science
- Health insurance
- 401(k)
Quick Apply

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Clinical Research Associate

Protagonist Therapeutics -
Newark, CA

Quick Apply

Job Details

$125,000 - $135,000 a year

Qualifications

Bachelor's degree
Pharmaceutical company experience

Full Job Description

Clinical Research Associate

Job Summary

Support ongoing trials and/or set-up and manage new trials.
Contributions include:
study planning and start-up,
project, site and vendor management
oversight of study site monitoring and performance
clinical operations input into the general clinical development of Protagonist compounds.

Skills & Attributes

Clinical trial experience that includes international Phase 1-2 trials, involving CROs from study set-up through to completion. Experience with Gastrointestinal, hematology and/or orphan drug trials preferred. High level of appreciation and understanding of the feasibility, regulatory and start-up processes, together along with on-site monitoring and site management. Good overall understanding of the major areas within clinical development. Excellent communication and interpersonal skills, along with attention to detail and critical thinking skills. Strong written and spoken English. Ability to collaborate, problem solve and work in a small dynamic organization with minimal supervision, to achieve personal and collective goals.

Experience Required

2+ years as a CRA within Biotech/Pharma or CRO

Education Required
Bachelors Degree

Travel Required
Yes, up to 10%

Core Responsibilities

Serves as the internal primary site operations lead, working with the Project Manager and CROs to achieve efficient study set-up and initiation, ongoing data monitoring all the way through successful study execution and site close-out.
Oversight of the site feasibility activities leading to site selection, activation and routine monitoring activities to ensure ongoing data integrity and quality.
Develops and reviews integrated site plans/timelines and reports weekly progress including risks and mitigations
Develops contingency plans for site performance, with regards to recruitment, data quality etc.
Helps ensure the trial stays within the contracted site management scope, progress, timelines and budget.
Presents site management strategy and status/metrics at project meetings.
Monitors and reports on CRO CRA resource utilization, and analyzes expected vs. actual performance
Implements and leverages best monitoring practices
Experience and proficiency with Good Clinical Practices (cGCP) and compliance with Protagonist SOPs
Works closely and effectively with other cross-functional teams to identify best practices and process improvements.
Proficiency with MS Office computer software
Other duties and assignments as requested for the overall performance of the function and Company.

The base pay range for this position at commencement of employment is expected to be between $125K and $135K / year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.

Protagonist Therapeutics is a discovery through late-stage development biopharmaceutical company. The Company's proprietary peptide technology platform enables de novo discovery of peptide therapeutics. Two novel peptides derived from Protagonist's proprietary discovery platform are at or near commercialization. ICOTYDE™ (icotrokinra) is approved in the U.S. for the treatment of moderate-to-severe plaque psoriasis in adults and pediatric patients 12 years of age and older who weigh at least 40 kg who are candidates for systemic therapy or phototherapy. ICOTYDE is the first and only targeted oral peptide that precisely blocks the Interleukin-23 receptor (IL-23R) licensed to Janssen Biotech, Inc.,a Johnson & Johnson company. ICOTYDE was jointly discovered by Protagonist and Johnson & Johnson scientists, with Protagonist having primary responsibility for the development of ICOTYDE through Phase 1, and Johnson & Johnson assuming responsibility for further development and commercialization. An NDA for rusfertide, a first-in-class hepcidin mimetic peptide that is being co-developed with Takeda Pharmaceuticals pursuant to a worldwide license and collaboration agreement entered in 2024, is under priority review with the FDA. Protagonist holds an option to co-commercialize rusfertide in the U.S. through a 50/50 profit and loss share structure or can opt-out of this structure. The Company also has a number of preclinical stage drug discovery programs addressing clinically and commercially validated targets including an oral IL-17 peptide antagonist, obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin programs.

More information on Protagonist, its pipeline drug candidates, and clinical studies can be found on the Company's website at https://www.protagonist-inc.com.

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Refine Your Search

clinical research associate jobs in fremont ca

Clinical Research Associate

Clinical Data Manager - II

Senior Clinical Research Associate

In House Clinical Research Associate

Neuroimaging Research Assistant

Clinical Research Coordinator Associate

Clinical Research Coordinator

Clinical Research Coordinator II

Clinical Data Manager

Clinical Research Coordinator 2

Senior Clinical Research Associate

Clinical Trial Manager - Contractor

Associate Director, Clinical Operations

Clinical Research Associate II

Clinical Research Manager

Clinical Research Associate

Clinical Research Coordinator – Cooperative Studies Program

Clinical Research Assistant – Exploratory Therapeutics Laboratory

Clinical Research Data Analyst II – Chronic Liver Diseases

Clinical Project Manager - Pleasanton, CA

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