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Clinical Trial Associate II (CTA II)

  • Job type: Permanent
  • Location: Boston
  • Salary: Competitive
  • Job reference: MM 923 32318
  • Sector: Clinical, Clinical Operartions, EPM Scientific
  • Date posted: 23/03/2018
Clinical Trial Associate II (CTA II)
  • Clinical Compliance/Protocol
  • Clinical Trials Phase I-IV
  • Greater Boston Area
A clinical phase III pharmaceutical company is actively seeking an innovative and motivated Clinical Trial Associate II to join their operations team. A leader in Rare Disease development finding a cure for the incurable.

Objective: Assist the study team across all investigator sites and ensures compliance with protocol and overall clinical objectives. Coordinate and track activities for clinical trials in compliance with protocol, Standard Operating Procedures (SOPs), and regulatory guidelines.

Duties (include but not limited to): Ensure study activities are executed according to study protocol, regulatory guidelines and operational plan. Review Investigational Drug Brochures (IDB), Protocols, Case Report Forms (CRFs) and informed consent forms (ICFs) for a thorough understanding of the study drug and procedures.

Qualifications:
  • Education: Graduate, postgraduate, 4-year college degree, or equivalent experience ideally in a scientific or healthcare discipline.
  • Experience:
    • Rare Disease experience is a plus
    • Pharmaceutical experience
    • Other:
      • 3 years or more in clinical operations, data management or related discipline either in CRO or pharmaceutical industry.
      • You must thrive in an entrepreneurial and autonomous environment where you will succeed based on your contribution and work ethic, not on your title or rank.
      • Ability to succeed in a fast-paced environment, become part of a close-knit team.
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