Senior Study Site Specialist

Pharmaceutical Research Associates, Inc
Canada
Remote
CAD 60,000 - 100,000
Job description

Overview

Under the guidance of the Director of Global Site Management & Central Services, this position will be responsible for participating in end-to-end site management from feasibility to site closure, serving as a point of contact for investigative sites and the study team members. This includes supporting site qualification, site level regulatory green light and site maintenance/close-outs.

Responsibilities

  • Participate in development of in-house model process documents.
  • For assigned sites and countries, serve as a primary site contact for end-to-end study activity.
  • Participate in all assigned Study Site Management study team meetings, providing cross-functional teams with detailed updates related to study and site activity.
  • Utilize systems and tools to track assigned activities and produce reports and metrics as needed.
  • Oversee essential document collection, tracking & review.
  • Support the collection of country and site level intelligence
  • Support Ethics Committee and Regulatory Authority submissions
  • Where required, complete, manage and/or support country and site-specific activities (e.g., compiling, submitting and obtaining import/export licenses, radiation board and biobank committee approvals, etc.) required to activate or maintain sites for a study as appropriate.

Qualifications

  • Bachelor’s Degree in Business Administration, Finance, science or related field.
  • Minimum of five years negotiating US Site contracts and budgets.
  • Minimum of five years of relevant experience in the biopharmaceutical/CRO industry.
  • Ability to negotiate complex contract and payment terms.
  • Flexibility to assume a workload which frequently necessitates an adjustment of priorities.
  • Goal oriented, self-starter with proven ability to work independently.
  • Able to proactively identify issues and provide potential solutions for resolution.
  • Detail oriented.
  • Ability to manage multiple tasks simultaneously and meet deliverables in accordance with stated timelines.
  • Proficiency with Veeva Vault and all applications of Microsoft Office.
  • Good interpersonal skills.
  • Comfort with ambiguity; ability to act without having the total picture.
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