Clinical Trial Transparency Senior Associate

Integrated Resources, Inc

  • Cambridge, Massachusetts
  • 7 days ago
  • Contractor
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Skills

  • Acceptance Testingunmatched
  • Biotech and Pharmaceuticalunmatched
  • Clinical Informationunmatched
  • Clinical Researchunmatched
  • Clinical Supportunmatched
  • Clinical Trialunmatched
  • Data Entryunmatched
  • Information Technology & Information Systemsunmatched
  • Maintain Complianceunmatched
  • Metricsunmatched
  • Process Analysisunmatched
  • Quality Controlunmatched
  • Rehabilitation Nursingunmatched

Description

Clinical Trial Transparency Senior AssociateIntegrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.Job DescriptionJob Title: Clinical Trial Transparency Senior AssociateLocation: Cambridge, MA Duration: 7+ months (Possibility of extension)• Performs the Clinical Trial Registration and/or results disclosure activities for new and/or ongoing studies.• Ensures compliance due dates are defined and timelines are met.• Collaborates with the Study Team to complete the data entry in support of Clinical Trial Disclosure, utilizing information from source documents and systems (e.g. protocol, CTMS).• Assigns tasks, initiates workflows, follows up on all action required, and escalates alerts when needed in order to maintain content that has been made public (e.g. clinicaltrials.gov).• Shares accurate information with various functional leads to be utilized throughout global disclosures• Performs internal quality control review of disclosure information.• Participates in User-Acceptance Testing (UAT) of disclosure system.• Supports process analysis efforts by identifying opportunities to improve the efficiency and effectiveness of the Clinical Trial Disclosure process.• Generates metrics for disclosure activities.• Supports the development and delivery of training materials.Requirements:• Firm understanding of Clinical Development and operations.• Previous experience ( 2-3 years minimum ) in pharma/biotech industry.• Must have previous experience disclosing clinical trial information on ClinicalTrials.gov.• Minimum education of Bachelor Degree (or equivalent experience).• Experience with PharmaCM would be a plus.

Numbers & Facts

LocationCambridge, Massachusetts
Job TypeContractor

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