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Clinical research associate Jobs in East orange nj

Last updated: 1 day ago
  • Promoted
Oncology Clinical Research Associate II

Oncology Clinical Research Associate II

ICON Strategic SolutionsNJ, United States
Full-time
Show moreLast updated: 30+ days ago
  • Promoted
Clinical Research Nurse

Clinical Research Nurse

ActalentHackensack, NJ, United States
$100,000.00–$120,000.00 yearly
Show moreLast updated: 18 days ago
  • Promoted
Research Associate

Research Associate

Stevens Institute Of TechnologyHoboken, New Jersey, US
Full-time
Show moreLast updated: 7 days ago
  • Promoted
Comprehensive Clinical Research and Drug Development

Comprehensive Clinical Research and Drug Development

VirbHackensack, NJ, United States
Part-time
Show moreLast updated: 2 days ago
  • Promoted
SENIOR ASSOCIATE, CLINICAL TRIAL MANAGER (CONTRACTOR)

SENIOR ASSOCIATE, CLINICAL TRIAL MANAGER (CONTRACTOR)

Amicus TherapeuticsNJ, United States
Full-time
Show moreLast updated: 1 day ago
  • Promoted
Associate Director, Cleanroom Operations

Associate Director, Cleanroom Operations

Bristol-Myers SquibbSummit, New Jersey, US
Full-time
Show moreLast updated: 8 days ago
  • Promoted
Clinical Research Associate

Clinical Research Associate

MeetNJ, United States
Full-time
Show moreLast updated: 25 days ago
Clinical Research Associate - Northeast

Clinical Research Associate - Northeast

PRA Health SciencesNJ, US
Show moreLast updated: 30+ days ago
Senior Clinical Research Associate - CNS - Northeast

Senior Clinical Research Associate - CNS - Northeast

Worldwide Clinical TrialsNew Jersey, USA
Show moreLast updated: 30+ days ago
  • Promoted
Clinical Research Study Manager

Clinical Research Study Manager

VitaliefNewark, NJ, United States
Show moreLast updated: 4 days ago
  • Promoted
Clinical Research Director, Neurology

Clinical Research Director, Neurology

ASB ResourcesNJ, United States
Full-time
Show moreLast updated: 20 days ago
Research Associate

Research Associate

Rutgers UniversityNewark, NJ
Show moreLast updated: 30+ days ago
Sr. Director, Clinical Research Scientist

Sr. Director, Clinical Research Scientist

KaztronixNJ, US
Quick Apply
Show moreLast updated: 30+ days ago
  • Promoted
Texas Licensed Clinical Research Associate

Texas Licensed Clinical Research Associate

VirtualVocationsNewark, New Jersey, United States
Full-time
Show moreLast updated: 1 day ago
Senior Clinical Research Associate - East Coast

Senior Clinical Research Associate - East Coast

BeiGeneUS, NJ, Home
$97,100.00–$132,100.00 yearly
Remote
Full-time
Show moreLast updated: 29 days ago
Clinical Research Nurse

Clinical Research Nurse

Hackensack Meridian HealthHackensack, NJ
Show moreLast updated: 30+ days ago
Clinical Instructor, Develop Innovation & Research

Clinical Instructor, Develop Innovation & Research

Cooperman Barnabas Medical CtrLivingston, NJ, US
Show moreLast updated: 30+ days ago
Research Associate

Research Associate

Stevens Institute of TechnologyHoboken, NJ, Main Campus
Full-time
Show moreLast updated: 30+ days ago
  • Promoted
Post Doctoral Research Associate

Post Doctoral Research Associate

New Jersey Institute of TechnologyNewark, NJ, United States
Full-time
Show moreLast updated: 30+ days ago
  • Promoted
Clinical Strategy Associate Director

Clinical Strategy Associate Director

Internet BrandsNewark, NJ, United States
Full-time
Show moreLast updated: 2 days ago
Oncology Clinical Research Associate II

Oncology Clinical Research Associate II

ICON Strategic SolutionsNJ, United States
30+ 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 New York or New Jersey (near a major airport)
  • Have a minimum of a B.Sc ., R.N., or equivalent degree, preferably in Biological Sciences
  • Have a minimum of 2 years’ experience in monitoring pharmaceutical industry clinical trials
  • Have a minimum of 2-3 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.