Job Market Guide: Clinical Research Coordinator jobs in San Francisco-Oakland-San Jose

Competition
Low
0.119017
Based on job seekers per open jobs
Desired Skills
Years of Experience
Years of Experience distribution graph for Clinical Research Coordinators in San Francisco-Oakland-San Jose. Clinical Research Coordinators in San Francisco-Oakland-San Jose have between ${} and ${} years of experience, averaging $${} years of experience.

39 Clinical Research Coordinator jobs in San Francisco-Oakland-San Jose

San Francisco, CA
Assist in the planning, implementation, managing, and reporting of Phase I-III clinical studies. In collaboration with other clinical staff and/or an external CRO, monitoring clinical trial conduct/metrics (enrollment, GCP practices, handling of safety issues, etc.)
industry
Biotech/Pharma
experience
Less than 5 years

South San Francisco, CA
Serve as a primary source of neuromuscular expertise for the study management team, clinical project team, and other internal and external stakeholders as required.
industry
Life Sciences & Research
experience
Not Specified

Redwood City, CA
Performs and reports laboratory testing on clinical laboratory samples used to aide physicians in the diagnosis and treatment of patients.
industry
Biotech/Pharma
experience
Less than 5 years

San Francisco, CA
Knowledgeable of clinical research operations, including interpretation and implementation of FDA regulations/ICH guidelines, is required.
industry
Life Sciences & Research
experience
Less than 5 years

South San Francisco, CA
The candidate will use their immunology knowledge and will master the molecular immunological techniques including molecular cloning, retroviral transduction, siRNA, western blotting, immuno precipitation, PCR, RT-PCR.
industry
Biotech/Pharma
experience
Less than 5 years

San Francisco, CA
In this role, you will be responsible for positively communicates and collaborates with colleagues, supervisors, and customers, both internal and external.
industry
Patient Care
experience
Less than 5 years

San Rafael, CA
Analyze, Model, simulate and predict nonclinical and clinical data to drive decisions on dose and frequency of dosing.
industry
Biotech/Pharma
experience
Less than 5 years

South San Francisco, CA
The primary responsibilities include, but are not limited to: designing complex quantitative pathology assays, and implementing new technologies to address key questions about our therapeutic candidates.
industry
Biotech/Pharma
experience
5 - 7 years

Sacramento, CA
The Clinical Coordinator plays a critical role in the successful implementation of telemedicine protocols for behavioral health patients in the emergency departments, inpatient units and in clinics at DHTN partner sites.
industry
Patient Care
experience
5 - 7 years

Santa Clara, CA
The candidate will work directly with pharmaceutical partners,clinical and R&D scientists, Clinical Trial Managers and regulatory affairs to assure compliance with internal and external requirements.
industry
IT Consulting/Services
experience
8 - 10 years

San Francisco, CA
This position is responsible for completing analyses and developing manuscripts for cohort studies at the San Francisco Coordinating Center (SFCC), focused on clinical and translational research about aging.
industry
Patient Care
experience
Less than 5 years

South San Francisco, CA
The candidate will use their immunology knowledge and will master the molecular immunological techniques including molecular cloning, retroviral transduction, siRNA, western blotting, immunoprecipitation, PCR, RT-PCR.
industry
Biotech/Pharma
experience
Less than 5 years

$90K - $130K - San Francisco, CA
This position will work closely with a cross-functional team to ensure that clinical trials are conducted in a timely fashion and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, company goals, and budgets.
industry
Biotech/Pharma
experience
Less than 5 years

South San Francisco, CA
Perform PK/PD analyses for small and large molecules from early to late drug development phase using state of the art modeling and simulation (M&S) techniques.
industry
Biotech/Pharma
experience
5 - 7 years

Daly City, CA
Coordinates Investigator and Study Coordinator meetings in collaboration with the Clinical Trial Manager.
industry
Biotech/Pharma
experience
Less than 5 years

Santa Clara, CA
Conducts team meetings, drafting and sending routine correspondence (e.g., newsletters) and/or by presenting regular updates to senior staff.
industry
Biotech/Pharma
experience
8 - 10 years

Sacramento, CA
The Clinical Coordinator is responsible for providing direction and clinical supervision of patient care.
industry
Patient Care
experience
Less than 5 years

Sacramento, CA
The incumbent is responsible for providing direction and clinical supervision of patient care for specific unit(s), patient population and assigned staff.
industry
Patient Care
experience
Not Specified

Pleasanton, CA
Works under general supervision, and participates in the design, planning, implementation and overall direction of clinical research projects.
industry
Biotech/Pharma
experience
Less than 5 years

San Rafael, CA
Interact with pharmacologists, toxicologists, medical directors and regulatory affairs personnel within for the timely completion of clinical and nonclinical studies and regulatory filings.
industry
Biotech/Pharma
experience
Not Specified

Santa Clara, CA
As a Clinical Affairs Scientist, your main responsibilities will be to determine clinical strategy in conjunction with team members, write clinical protocols, analyze data and write reports to support the clinical documentation of Companion Diagnostics (CDx)in the field of tissue-based Cancer Diagnostics.
industry
Business Services
experience
8 - 10 years

Redwood City, CA
Performs and reports laboratory testing on clinical laboratory samples used to aide physicians in the diagnosis and treatment of patients.
industry
Biotech/Pharma
experience
Less than 5 years

San Francisco, CA
The Clinical Scientist will be a key contributor in building an integrated development plan in late development and will provide support to new development activities, as well as clinical guidance and assessment of future opportunities to advance the science and address unmet needs in oncology clinical development.
industry
Biotech/Pharma
experience
5 - 7 years

San Francisco, CA
The Clinical Research Associate (CRA) conducts site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study, Site Initiation, Routine Monitoring, and Close-out Visits.
industry
Biotech/Pharma
experience
5 - 7 years