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Clinical research associate Jobs in Elk grove ca

Last updated: 12 hours ago
  • Promoted
Oncology Clinical Research Associate II

Oncology Clinical Research Associate II

ICON Strategic SolutionsCA, United States
Full-time
Show moreLast updated: 5 days ago
  • Promoted
Registered Nurse - Clinical Research

Registered Nurse - Clinical Research

CSMN - 1101141 - Cardiology - TowersCA, United States
Full-time
Show moreLast updated: 7 days ago
  • Promoted
  • New!
CLINICAL RESEARCH COORDINATOR I (HYBRID)

CLINICAL RESEARCH COORDINATOR I (HYBRID)

CEDARS-SINAICA, United States
$23.39–$39.76 hourly
Full-time
Show moreLast updated: 12 hours ago
Research Associate

Research Associate

R&D PartnersCalifornia, CA
Show moreLast updated: 30+ days ago
  • Promoted
  • New!
CLINICAL TRIAL ASSOCIATE

CLINICAL TRIAL ASSOCIATE

Bayside Solutions, Inc.CA, United States
Full-time
Show moreLast updated: 12 hours ago
  • Promoted
  • New!
REGISTERED NURSE - CLINICAL RESEARCH NURSE (CRN)

REGISTERED NURSE - CLINICAL RESEARCH NURSE (CRN)

J. Edward Staffing LLCCA, United States
Temporary
Show moreLast updated: 12 hours ago
  • Promoted
Clinical Research Associate

Clinical Research Associate

MeetCA, United States
Full-time
Show moreLast updated: 5 days ago
  • Promoted
Research Associate III - Histology

Research Associate III - Histology

Hydrogen GroupCA, United States
Full-time
Show moreLast updated: 10 days ago
  • Promoted
Clinical Research Coordinator

Clinical Research Coordinator

SF Research InstituteCA, United States
$80,000.00 yearly
Full-time
Show moreLast updated: 23 days ago
Clinical Research Associate I - Biomedical Imaging Research Institute

Clinical Research Associate I - Biomedical Imaging Research Institute

Cedars-SinaiCA, United States
Show moreLast updated: 27 days ago
  • Promoted
  • New!
CLINICAL TRIAL ASSOCIATE

CLINICAL TRIAL ASSOCIATE

Summit Therapeutics plcCA, United States
$100,000.00–$115,000.00 yearly
Full-time
Show moreLast updated: 12 hours ago
  • Promoted
  • New!
MEDICAL ASSISTANT - CLINICAL RESEARCH

MEDICAL ASSISTANT - CLINICAL RESEARCH

CenExelCA, United States
$21.00–$23.00 hourly
Full-time
Show moreLast updated: 12 hours ago
  • Promoted
Associate Clinical Scientist

Associate Clinical Scientist

Bayside SolutionsCA, United States
$83,200.00–$104,000.00 yearly
Full-time
Show moreLast updated: 5 days ago
Oncology Clinical Research Associate II

Oncology Clinical Research Associate II

ICON Strategic SolutionsCA, United States
5 days ago
Job type
  • Full-time
Job description

What will you be doing?

  • Works on multiple oncology trials
  • Quality of life focus wtih Regional Travel
  • Demonstrated leadership, through involvement in specific initiatives when needed, and / or SME to systems and / or processes
  • Mentors / coaches junior flex team
  • Acts as Lead SM-training other SMs on study
  • Develops site start up documents for studies including SIV agenda
  • Provides SM “voice” when reviewing study documents (e.g. Monitoring Guidelines)
  • Represents LTMs or SMs on SMTs / meetings
  • Takes over LTM role reports review (SQV, SMV, SCV) for sites assigned to other SMs from the same trial
  • Supports country budget development and / or contract negotiation in liaison with CCS colleagues
  • Assists with ASV
  • Metrics / KPIs : Metrics / KPIs governing these services are outlined in the Quality Oversight Plan (QOP) document.

Interfaces – Primary / Other :

  • Primary interfaces : Provider Functional Manager, Clinical Trial Assistant, Local Trial Manager and Central Study Team for assigned clinical trials.
  • Other Interfaces : Study Responsible Physician, Regional Quality and Compliance. Manager / Specialist, Local Drug Safety Officer (where required) and Site Manager team; Investigators and their delegates at site (trial personnel including study coordinators, pharmacists, etc.)
  • Qualifications Needed :

  • Based in the California (near a major airport)
  • Have a minimum of a B.Sc ., R.N., or equivalent degree, preferably in Biological Sciences
  • Have a minimum of 3 years’ experience in monitoring pharmaceutical industry clinical trials
  • Have a minimum of 1-3 years' experience monitoring Oncology trials
  • Knowledge of several therapeutic areas, with oncology an asset but not a requirement.
  • Analytical / risk-based monitoring experience is an asset
  • Ability to actively drive patient recruitment strategies at assigned sites
  • Ability to partner closely with investigator and site staff to meet all of our study timelines
  • Ability to operate and use various systems and databases (e.g. CTMS, EDC, eTMF, various dashboards / metrics, IWRS, safety reporting).
  • Possess strong communication and influencing skills to effectively manage study sites both remotely and face to face. Strong team member and self-starter with the ability to work independently.
  • Have an in-depth knowledge of Good Clinical Practice, ICH guidelines and local regulatory requirements.
  • Need to travel up to 50%
  • What ICON can offer you :

    Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

    In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

    Our benefits examples include :

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
  • Visit our careers website to read more about the benefits of working at ICON :

    At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

    Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.