Senior Clinical Trial Associate

Cambridge, MA 02139

Posted: 11/14/2019 Employment Type: Contract Industry: Clinical & Scientific Job Number: 16750

Job Description


Bayside Solutions is seeking a Senior Clinical Trial Associate to be part of our client’ s team in Cambridge, MA. This is an opportunity to work with the largest pharmaceutical corporation in the world and leading pharmaceutical corporations.

Our Client is the global leader in a variety of influenza vaccines with a goal to lessen the severity and impact of influenza. With a global focus on influenza, they work with cutting-edge research, transformative technologies and the latest methods of production and distribution.

Our Company Bio:  Bayside Solutions was founded in 2001, Bayside was recognized as one of the fastest growing professional staffing companies in Northern California. The numbers tell the story: We have close to a 100% client retention rate, 700% growth in four plus years and over 95% repeat business. Our dedication to building partnership relationships with both our clients and our recruits is the key to our phenomenal success.

You can find additional information on our company website at www.baysidesolutions.com.

Senior Clinical Trial Associate

Job Benefits:
  • An opportunity to join a patient-focused organization that is driven to develop, manufacture and commercialize medicines to treat life threatening conditions.
  • Work for a company that is local to the bay area and recognized as a leader of innovation.
  • Competitive compensation commensurate with experience.
  • This position is eligible for medical, vision, dental benefits, paid sick time, and 401K.

Summary of Responsibilities:
  • Support the planning and conduct of clinical studies as a member of the study execution team (SET).
  • Provide support to the Clinical Development Therapeutic Area in preparing CSRs and clinical packages for regulatory submissions
  • Provides cross-functional support for other ongoing activities including inspection readiness preparations. 
  • Responsible for study documentation and filing, as well as timeline tracking and reporting.
  • Provide organizational and logistical support for compliance-related activities, including study management, site management, monitoring oversight and trial file (TMF) management.

Summary of Qualifications:
  • BSc/MS/PhD in an Allied Medical discipline or Pharmacy with 6 months+ experience in the pharmaceutical/biotechnology industry.
  • Ability to adapt to changing priorities and deliver objectives in a complex matrix environment.
  • Strong presentation skills with the ability to articulate key information.
  • Excellent project management skills with strong attention to detail.
  • Proactively owns and drives assigned tasks to completion
  • Systems proficiency in MS Office Suite (PowerPoint, Excel, and Word)

Meet Your Recruiter

Allison Glogovac

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