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...Job Summary:
The Clinical Trial Nurse Manager (CTN-Manager) position assists in the administrative leadership and direction of... ...clinical trials program. This position oversees clinical trial research activities of non-physician research personnel in a manner that...
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...Job Title: Clinical Research Associate - B
Location: Alameda, CA (94502)
Shift – 8:00am to 5:00pm
Duration: 6 Months with possible... ....
Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure...
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...biologic and peptide drugs. We are advancing a clinical‐stage pipeline of differentiated... ...location.
POSITION SUMMARY
The Clinical Research Associate (CRA) will independently... ...will be responsible for implementing and monitoring clinical study activities to assure adherence...
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...Responsibilities:
~ As a vital member of our clinical team, the Clinical Research Associate will be responsible for conducting Phase I-IV single... ...assembling submissions related to study protocols.
Monitoring investigational sites to ensure protocol adherence....
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...Position Title: Clinical Research Associate
Reports to: Associate Director, Clinical Operations
Status: Regular, Full-time, Exempt... ...-house CRA responsibilities). You will not conduct on-site monitoring activities and there is very little to no travel involved....
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...investors such as CVS Health Ventures and Blackstone Horizon
THE JOB AT A GLANCE
We're looking for a Research Coordinator to provide research support for clinical studies run by Carbon Health's clinical research program, Carbon for Research. If you are passionate...
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...Job Summary
The Helen Diller Family Comprehensive Cancer Center (HDFCCC) Clinical Research Network Office is seeking a Clinical Research Coordinator (CRC) to support the I-SPY Program at UCSF Cancer Center Berkeley.
UCSF is the lead site for the I-SPY Program; the...
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Clinical Research Associate II
Contract: Alameda, California, US
Salary:... ...Perform study site visits (SQV, SIV, IMV, COV), generate monitoring trip reports, and track resolution of action items.
Participate...
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Pay: $59.00 - 55.00
Tmber of the clinical team responsible for conducting Phase I-IV single... ...case report forms (CRFs), Contract Research Organization (CRO) selection and management... ...for writing basic study protocols, monitoring or overseeing monitoring of investigational...
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...Description:**
The SCRA is primarily a site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and... ...complex or diverse information; Collects and researches data; Uses intuition and experience to complement...
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...Role : Clinical Research Associate (CRA) - B
Location : Alameda, CA - 94502
Duration : 6 Months on W2
Shift Timings... ...Skills Looking For:
- Direct on-site monitoring experience is required.
- Experience in conducting SQV, SIV...
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...Job Description
Responsible for providing Clinical Research support for all clinical trials. Under the direction of supervisor or designee... ..., and other necessary materials.
Conduct ongoing study monitoring, including frequent periodic site visits, protocol adherence...
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...Position Definition :
The Clinical Research Coordinator will plan, direct, or coordinate clinical research projects, and will evaluate... ..., and other activities to advance research productivity.
Monitors study activities to ensure compliance with protocols and relevant...
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...Position Definition :
Under the supervision of Principal Investigator (PI), the clinical research coordinator (CRC) will perform duties related to the support and coordination of clinical research studies and may receive training and development to prepare and advance...
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...Director, Clinical Research Informatics
About the Company
Esteemed community-based healthcare system
Industry
Hospital & Health Care
Type
Privately Held
About the Role
The Director, Clinical Research Informatics will be responsible for developing...
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...Job Summary:
The Clinical Trial Research Coordinator I (CTRC-I) is a novice level position which, under the clinical direction of the Principal... ..., assist with preparation for inspections, audits and monitoring visits.
Study Implementation Maintain the security and...
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Title: Clinical Research Associate
Duration: 06 Months with possible extension
Location: Alameda, CA, 94502
Description:
Note:... ...submissions. Responsible for writing basic study protocols, monitoring or overseeing monitoring of investigational sites to ensure...
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...to drive better-informed decisions. We're revolutionizing the way people monitor their glucose levels with our new sensing technology.
The Opportunity
We are looking for a Clinical Research Associate I, to support the Study Start Up team. In this role, candidate...
We are looking for a per diem Phlebotomist to join our Clinical Research Team.
Must have previous blood draw experience.
Visit activities include but are not limited to:
Collect Vital Signs
Check for Hospitalizations
Check for Concomitant Medications...
Weekday work
...Research Associate I
Req ID #: 222596
Location:
S. SanFrancisco, CA, US, 94080
For 75 years, Charles... ...+ Basic tissue and blood collection.
+ In-life monitoring of the study animals for body weights, clinical observations, tumor measurements, etc.
+ Monitor...
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