Senior Clinical Research Associate - Alzheimer's/Dementia - (Virtual in the Northeast)

Multiple Locations: New Jersey, United States • King of Prussia, Pennsylvania, United States • New York, United States • Massachusetts, United States • Pennsylvania, United States • Maryland, United States • Connecticut, United States • Delaware, United States

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Requisition Number: 2363

Position Title: Senior Clinical Research Associate

External Description:

Our Senior Clinical Research Associates (CRA) are home-based. They are responsible for site qualification, initiation, interim monitoring, site management and study close-out visits for studies in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs). Ensure quality of data submitted from study sites and assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel. This particular role will focus on CNS, specifically Alzheimer’s Disease.

*This virtual position is home-based and offers a competitive salary and a $5,000 USD sign-on bonus!

Note: We are accepting resumes (CV) from experienced CRAs in Northeastern US
 
RESPONSIBILITIES:

  • Write site visit trip reports
  • Compile and ensure completeness of regulatory documents and ethical submission documentation as appropriate and required (e.g. IRB / IEC study approval, informed consent, etc.)
  • Coordinate study material (e.g. CRFs, manuals) shipment and receipt by study site
  • Document site visit findings via written reports
  • Review study subject safety information and informed consent
  • Conduct source document verification for compliance, patient safety, and veracity of data
  • Review CRFs using paper or electronic data capture systems and assist sites with data query resolution
  • Maintain regular communication with sites

 
REQUIREMENTS:

  • Requires a bachelor’s degree or a two-year nursing degree
  • A minimum of 5 years’ field monitoring experience required
  • Alzheimer’s or Dementia monitoring experience required
  • Willingness to travel required
  • Valid current passport required
  • Driving license required
  • Fluent in the local languages of the countries under responsibilities and proficient in both spoken and written English

    Worldwide Clinical Trials is an Equal Opportunity Employer

 

#UncommonCRO

#LI-NJ1

#LI-Remote

 

City:

State: Pennsylvania

Employment Type: Regular

Community / Marketing Title: Senior Clinical Research Associate - Alzheimer's/Dementia - (Virtual in the Northeast)

Company Profile:

We’re a global, mid-size CRO that pushes boundaries, innovates and invents — because the path to a cure for the world’s most persist diseases is not paved by those who play it safe, but by those who take pioneering, creative approaches, and implement them with quality and excellence. We are experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs, in the best possible way.

Location_formattedLocationLong: King of Prussia, Pennsylvania US

CountryEEOText_Description: Worldwide Clinical Trials is an equal opportunity employer, dedicated to a policy of non-discrimination in employment on any basis including age, sex, color, race, creed, national origin, religion, marital status, sexual orientation, political belief or disability.

 Worldwide Clinical Trials does not accept unsolicited resumes from 3rd party vendors

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© Worldwide Clinical Trials 2019

We only accept resumes from staffing organizations with pre-approved contractual agreements. Please do not forward resumes directly to our hiring managers, jobs alias, or any other company location. Unsolicited resumes from employment agencies will not be considered and Worldwide is not responsible for any fees related to unsolicited resumes.