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Clinical Research Coordinator Associate Jobs in Mountain View, Santa Clara, California

Clinical Research Associate Jobs
By Integrated Resources, Inc ( IRI ) At Mountain View, CA, United States
The Clinical Research Intern will apply analytical, project management skills and enthusiasm for healthcare and commitment to improving healthcare through research.
The candidate will Product practical experience within the Clinical Research operations at ***.
Complies with established policies, health and safety regulations and requirements, procedures, and department objectives.
Bachelor's Degree in biological or life sciences or health related field OR attending/completed a clinical research certification program.
Proficient computer skills using Microsoft Office products.
May assist with follow up and closing of clinical studies.
Clinical Research Associate Jobs
By Intuitive At Sunnyvale, CA, United States
Clinical research/clinical trial management certification/education preferred
Must be clinically savvy and possess time management, organizational skills and problem-solving skills
Skills, Experience, Education, & Training:
Perform on-site (preferred) and remote (as needed) site qualification visits, site initiation visits, interim monitoring visits and close out visits.
Collaborate with data management to support CRF build, amendment, and data cleaning process.
Manage site start-up and activation process, including:
Cancer Clinical Research Coordinator Associate - Hematology
By Stanford University School of Medicine At Stanford, CA, United States
Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
Knowledge, Skills And Abilities (required)
Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
Knowledge of the principles of clinical research and federal regulations.
Previous experience with clinical research.
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
Cra (Clinical Research Associate)
By Agilent Technologies At Santa Clara, CA, United States
Assist with site audits and site quality management activities, as needed.
Please update the minimum qualifications below to reflect the requirements for your specific role.
Ensure monitoring activities (remote and on-site) are completed in accordance with Agilent procedures and study monitoring plan.
Assures adherence to GCP, study protocol, and all applicable requirements through routine monitoring visits.
3+ years direct clinical research experience at a sponsor or CRO as a CRA/study monitor, or equivalent experience.
Diagnostic/IVD experience highly preferred, oncology or other medical device experience is also accepted.
Clinical Research Coordinator Jobs
By SMCI At San Francisco Bay Area, United States
Education: BS/BA degree in a life science, health science, RN, or related field.
2+ years of professional working experience as a Clinical Research Coordinator.
Working knowledge of GCP and FDA Regulations.
Excellent oral and written communication skills.
Strong attention to detail and organizational skills.
Experience utilizing Electronic Data Capture (EDC) systems for clinical studies.
Clinical Research Coordinator Jobs
By Rady Children's Hospital-San Diego At San Diego County, CA, United States

Job Summary: Initiates & manages multiple cooperative group trials such as Children's Oncology Group (COG) clinical trials related to pediatric cancer to include, but not limited to: execution ...

Dps Clinical Research Coordinator
By City of Hope At Duarte, CA, United States
Bachelor’s Degree or Certified CRA or Certified Tumor Registrar in lieu of degree. Experience may substitute for minimum education requirements.
Basic education, experience and skills required for consideration:
Preferred education, experience and skills:
Conducts protocol database management for an assigned set of multiple research protocols.
Makes recommendations and participates in Policy and Procedure development regarding particular areas of team assignment and general data management issues.
Identifies and communicates important protocol and data management issues or problem areas to supervisor.
Clinical Research Associate Jobs
By Vial At San Francisco, CA, United States
Site management and monitoring activities across all US clinics
Minimum of 2 years work experience as a Clinical Research Associate
You should be life science degree educated with independent on-site monitoring experience.
Flexibility and ability to travel are paramount with strong communication, written and presentation skills.
Must have experience in Dermatology and Ophthalmology studies.
Work with sites to adapt, drive and track subject recruitment plan
Clinical Research Associate (Cra) - B
By Intellectt Inc At Alameda, CA, United States
5+ years of relevant experience in site monitoring and clinical project management.
Project management and organizational skills.
Communicate study progress to management.
Understanding of clinical trial process, data management, and analysis.
Manage clinical monitoring, site compliance, and adherence to protocols.
Experience in medical device, in-vitro diagnostics, or pharmaceutical studies.
Clinical Research Coordinator Jobs
By care.coach At Millbrae, CA, United States
Strong attention to detail & time management skills
Implement and manage clinical research projects with internal and external stakeholders across the country in hospital and community-based settings
Obtain IRB approval and maintain compliance with OHRP and other federal regulatory requirements
3+ years of research coordination experience and independence (can be pre-doctoral)
Experience with older adults and ab/normal age-related decline
Grant writing and clinical trial (RCT) experience
Clinical Research Associate Jobs
By ProKatchers LLC At West Sacramento, CA, United States
Position Requirements: Bachelor's degree in a Life Science or related field with 2+ years’ experience in laboratory experience.
Location:West Sacramento CA 95691 United States
Pay Rate:$45/ HR to $50/ HR
Clinical Research Associate Jobs
By KlinEra Global Services At San Francisco Bay Area, United States
Excellent interpersonal, judgment, and time management
You will also manage regular site liaison, tracking, query resolution, and maintaining investigator site file and TMF.
Approximately 3-5yr Experience as Clinical Research Associate
Fundamental knowledge and good understanding of GCP’s, clinical study development process, and logistics.
Proficient knowledge of MS Office Applications (Word, Excel, PowerPoint, Etc.
Support study start-up activities including site selection, collecting essential documents and CTRA, register study on ANZCTR.
Clinical Research Coordinator Jobs
By Care Access At Los Gatos, CA, United States
Good management and organizational skills, understanding of medical procedures
Serving as the primary contact to ensure appropriate communications, trial management, and meeting of timelines
Exceptional interpersonal skills, the ability to work independently
Phlebotomy experience is a plus
Experience checking and documenting vitals and EKG (ECG) within the past year.
Benefits (US Full-Time Employees Only)
Clinical Research Coordinator Jobs
By Insight Global At Spring Valley, CA, United States
Desired Skills and Experience *
Data Entry, Administrative needs - i.e. Filing, set-up for upcoming appts, organizing documentation, and Patient consenting
PART TIME- 20 Hours Per Week
Contract Duration: 6 Months with potential to extend!
Clinical Research Associate Jobs
By Jobot At Los Angeles, CA, United States
Strong Benefits And Compensation Package
Clinical Research Associate opportunity in the oncology space!
Want to learn more about this role and Jobot?
Clinical Research Associate Ii
By DermTech At San Diego Metropolitan Area, United States
Effective time and financial management skills.
Or equivalent combination of education and experience
or equivalent combination of education and experience
Years of independent monitoring experience within a Contract Research Organization/Pharmaceutical company
Good therapeutic and protocol knowledge as provided in-company training.
Strong written and verbal communication skills including good command of the English language.
Clinical Research Coordinator Jobs
By City of Hope At Irvine, CA, United States
Bachelor’s Degree. Experience may substitute for minimum education requirements (Associate Degree plus minimum of 2 years of experience).
Two or more years of experience related to the management and conduct of oncology clinical trials in an academic setting.
Basic education, experience and skills required for consideration:
Meets contractual or institutional requirements for timeliness of data entry and query resolution.
Identifies and communicates important protocol and data management issues or problems to the PI and supervisor in a timely manner.
Working knowledge of clinical trials, Federal, State, and Local Regulations, IRB requirements, consent form and protocol development.
Clinical Research Associate Jobs
By Compliance Group Inc At Alameda, CA, United States

Description: Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal Regulations and ICH guidelines. Responsible for assisting senior ...

Clinical Research Associate Jobs
By Aven Talent Resources At Solana Beach, CA, United States
 Manage sample inventory with superior organizational skills
 Superior molecular biology bench skills with great attention to details
 Experience with nucleic acid technologies relating to PCR and qPCR required
 Prior experience in oncology and NGS prefered
 Experience in liquid biopsy is a plus
 Experience working under design control highly desired
Clinical Research Coordinator Jobs
By ProSciento, Inc. At Chula Vista, CA, United States
Keeps the Clinical Trial Management System (CTMS) updated with pertinent information.
Functional/Technical Skills: Has the functional and technical knowledge and skills to do the job at a high level of accomplishment.
Time Management: Uses his/her time effectively and efficiently; values time; concentrates his/her efforts on the more important priorities.
Assists with data entry, as needed.
Communicates with study subjects regarding their study status and enrolment into the study.
Schedules subject appointments, performs subject reminder calls, and instructs subjects regarding any medication washout per protocol.
Clinical Research Coordinator Jobs
By Truvian At San Diego, CA, United States
Maintain working knowledge of multiple Institutional Review Boards (IRB) approved protocols and assist with data entry as needed
Clinical Site Management, including implementation of associated processes and documentations
Manage sign up calendar for available appointments for upcoming studies
Manage phlebotomist scheduling with external vendor
Record adverse events for donors experience in draw session
Maintain good record keeping of compensation log per donor and collaborate with Finance team to address pay out concerns
Clinical Research Associate Jobs
By USC At , San Diego, Ca $42.26 - $52.60 an hour
Confirm sites are following GCP, regulatory requirements, study protocol, and ATRI policies. Work with sites to document deviations from standard procedures.
Experience in AD research is preferred.
Act as main point of contact for assigned clinical sites.
Thorough understanding of study protocol and manuals.
Work closely with Lead Clinical Monitor/Lead CRA to escalate site compliance issues.
Participate in monitoring activities to achieve study milestones.
Clinical Research Associate Jobs
By Infosoft, Inc. At Irvine, CA, United States
Solid understanding and knowledge of principles, theories, and concepts relevant to clinical trial management
3 years of previous hands-onclinical researchexperience
Good computer skills in usage of MS Office Suite including MS Project and excellent Excel skills required
Excellent written and verbal communication skills and interpersonal relationship skills
Solid knowledge of human anatomy and physiology
Good problem-solving, organizational, analytical, and critical thinking skills