Clinical research manager Jobs in Sunnyvale, CA
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Clinical research manager • sunnyvale ca
Last updated: 6 hours ago
Support the successful execution of clinical studies by contributing to study design, documentation, and overall management.
Lead and manage site start-up and activation processes, including regulat...Show moreLast updated: 17 days ago
At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing.Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solution...Show moreLast updated: 27 days ago
Assistant Clinical Research Coordinator School of Medicine, Stanford, California, United States NewResearch4 days ago Post Date106779 Requisition # The Division of Cardiovascular Medicine , within ...Show moreLast updated: 3 days ago
About QED Therapeutics & BridgeBio PharmaQED Therapeutics, an affiliate of BridgeBio Pharma, focuses on developing targeted treatments for FGFR-driven skeletal dysplasias, particularly Achondroplas...Show moreLast updated: 30+ days ago
You are applying for a position through Medix, a staffing agency.The actual posting represents a position at one of our clients.
This is a fixed-term Clinical Research Associate / Data Manager positio...Show moreLast updated: 2 days ago
Abbott is a global healthcare leader that helps people live more fully at all stages of life.Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses an...Show moreLast updated: 6 hours ago
OVERVIEWThis role will lead the coordination of research in an exciting new environment, with the full backing of a new type of research architecture and a top-tier technology team, challenging the...Show moreLast updated: 30+ days ago
Our client, [Industry Descriptor] is seeking a [Job Title] to join their team.As a [Job Title], you will be part of the [Department Name] supporting [Team Name(s)].
The ideal candidate will have [So...Show moreLast updated: 15 days ago
Onsite (5 days / week, occasionally 1 remote).Clinical studies supporting medical device and wearable technology development.
Execute end-to-end clinical studies under IRB protocol.Tasks include : prot...Show moreLast updated: 30+ days ago
Develops product-critical physiological data-collection protocols and executes studies according to good laboratory practice, following applicable health and safety principles and practices.Prepare...Show moreLast updated: 23 days ago
Mountain View, CA; hybrid role (on-site 4 days a week).Develops product-critical physiological data-collection protocols and executes studies according to good laboratory practice, following applic...Show moreLast updated: 30+ days ago
Develops product-critical physiological data-collection protocols and executes studies according to good laboratory practice, following applicable health and safety principles and practices.Prepare...Show moreLast updated: 5 days ago
Abbott is a global healthcare leader that helps people live more fully at all stages of life.Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses an...Show moreLast updated: 3 days ago
A company is looking for a Senior Manager, Clinical Research.Key Responsibilities Serve as liaison for trial vendors and manage PD GENEration research coordinators Oversee site selection, enroll...Show moreLast updated: 3 days ago
A global device company is looking for a motivated Clinical Research Associate III to support studies involving wearable sensor technology and human subject data collection.Key responsibilities inc...Show moreLast updated: 3 days ago
Develops product-critical physiological data-collection protocols and executes studies according to good laboratory practice, following applicable health and safety principles and practices.Prepare...Show moreLast updated: 30+ days ago
We are proactively identifying candidates for a potential.Clinical Research Associate (CRA).Responsibilities may include site communication, vendor oversight, document management, TMF review, and d...Show moreLast updated: 18 days ago
- Promoted
Clinical Research Associate
GForce Life SciencesSunnyvale, CA, USTemporary
- Promoted
Senior Clinical Research Scientist
Danaher CorporationSunnyvale, CA, United StatesFull-time
- Promoted
Assistant Clinical Research Coordinator
Westfield State CollegePalo Alto, CA, United StatesFull-time
Clinical Research Associate
BridgeBio Pharma, Inc.San Jose, CA, United StatesFull-time
Clinical Research Associate / Data Manager
MedixPalo Alto, CA, USTemporary
- New!
Director Clinical Research
AbbottSanta Clara, CA, USFull-time
Clinical Research Nurse
Topography HealthSan Jose, CA, United StatesFull-time
Clinical Research Associate
ExperisPalo Alto, CA, USFull-time
Clinical Research Associate
The Fountain GroupMountain View, CAFull-time
Clinical Research Associate
Cypress HCMMountain View, CAFull-time
Clinical Research Associate
FocusKPI Inc.Mountain View, CA, USTemporary
Clinical Research Associate
Ryzen SolutionsMountain View, CAFull-time
- Promoted
Sr. Scientist Clinical Research
Society of Exploration GeophysicistsSanta Clara, CA, United StatesFull-time
Senior Manager of Clinical Research
VirtualVocationsSunnyvale, California, United StatesFull-time
- Promoted
Clinical Research Associate
OSI EngineeringMountain View, CA, United StatesFull-time
Clinical Research Associate III
HireTalentMountain View, CA, USFull-time
Senior clinical research associate
RandstadMenlo Park, CA, USPart-time
- dentist (from $ 183,150 to $ 250,000 year)
- general dentist (from $ 230,000 to $ 250,000 year)
- technical director (from $ 102,500 to $ 243,250 year)
- digital artist (from $ 190,783 to $ 243,100 year)
- medical director (from $ 172,500 to $ 242,000 year)
- computer engineer (from $ 148,200 to $ 241,000 year)
- database engineer (from $ 100,425 to $ 240,000 year)
- engineering director (from $ 187,500 to $ 240,000 year)
- product director (from $ 180,000 to $ 238,642 year)
- embedded systems engineer (from $ 163,500 to $ 234,000 year)
- New York, NY (from $ 89,641 to $ 168,580 year)
- Indianapolis, IN (from $ 75,000 to $ 168,580 year)
- Nashville, TN (from $ 138,500 to $ 168,580 year)
- Raleigh, NC (from $ 102,940 to $ 165,643 year)
- Honolulu, HI (from $ 115,750 to $ 164,202 year)
- Jersey City, NJ (from $ 78,285 to $ 160,219 year)
- Oklahoma City, OK (from $ 78,352 to $ 158,850 year)
- Salt Lake City, UT (from $ 78,509 to $ 158,850 year)
- Kansas City, MO (from $ 78,285 to $ 158,850 year)
- Kansas City, KS (from $ 78,285 to $ 158,850 year)
The average salary range is between $ 78,459 and $ 133,765 year , with the average salary hovering around $ 95,116 year .
Clinical Research Associate
GForce Life SciencesSunnyvale, CA, US17 days ago
Job type
- Temporary
Job descriptionExperience implementing and managing medical device clinical trials. In-depth knowledge of ISO 14155, 21 CFR Part 11, 50, 54, 812, and ICH / GCP regulations. Proficiency in developing study documents (protocols, informed consent forms, CRFs / eCRFs, monitoring plans). Experience with clinical research budgeting and contract negotiation. Proficiency with Microsoft Office Suite, PDF applications, and Electronic Data Capture (EDC) systems. Experience with Clinical Trial Management Systems (CTMS). Prior experience in protocol and clinical section writing for regulatory submissions. Experience in medical device industry is required. Experience with IDE (pre-market) studies.
Job Description
Sr. Clinical Research Associate
12-month contract
Onsite in Sunnyvale, CA
Responsibilities
- Support the successful execution of clinical studies by contributing to study design, documentation, and overall management.
- Lead and manage site start-up and activation processes, including regulatory document preparation, IRB / EC submissions, and clinical trial agreements.
- Conduct monitoring visits (qualification, initiation, interim, and close-out) and ensure protocol and regulatory compliance through source data verification and study oversight.
- Serve as the primary liaison for clinical sites, overseeing data entry, investigational device tracking, and issue resolution.
- Maintain and manage study documentation, including Trial Master File (TMF), clinical trial management systems (CTMS), and site payments.
Qualifications