Sr. Clinical Research Associate - NASH - Northeast

Multiple Locations: New York, NY, USA • Massachusetts, USA • Pennsylvania, USA • Connecticut, USA • Vermont, USA • Rhode Island, USA • New Hampshire, USA • Maine, USA • New Jersey, USA

Notice

This position is no longer open.

Requisition Number: 2569

Position Title: Senior Clinical Research Associate

External Description:

We're uncommon. A willingness to take the road less traveled to meet the demands of your trial isn't always accepted by CROs, but at Worldwide, we're committed to your specific needs. We never take a "one size fits all approach."

Our Clinical Research Associates (CRA) are home-based and have 8 on-site days monthly. 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 NASH.
 
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 2 years’ field monitoring experience required
  • Monitoring experience in NASH preferred 
  • 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-MK2

#LI-Remote

City:

State: Pennsylvania

Employment Type: Regular

Community / Marketing Title: Sr. Clinical Research Associate - NASH - 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.

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© Worldwide Clinical Trials 2023

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.