Site Oversight & Operations Relationship Lead (Contractor)


Company Name: Pfizer
Location: Turkey
The Site Oversight & Operations Relationship Lead is the main Pfizer point of contact for investigative sites as well as accountable for safeguarding the quality and patient safety at the investigator site. This role is responsible for site monitoring and oversight and building and retaining relationships from site activation through the lifecycle of studies. As part of the oversight responsibilities, this role will utilize and interpret data from analytic tools, in conjunction with country and regional intelligence to proactively identify risks to quality and compliance and to develop and implement mitigation plans to address these risks. This role is also accountable for identifying CRA performance issues and is responsible for ensuring appropriate corrective and preventative actions are put in place.

The Site Oversight & Operations Relationship Lead proactively collaborates and provides local intelligence to country outreach surveys, sites strategies, study design, and Pfizer pipeline opportunities. This role is accountable for study start up, activation, and execution to the plan for targeted sites. In addition to being the main point of contact, the lead will help coordinate with other roles and functions that will interface with target sites, thereby, simplifying site Pfizer communications and enhancing overall visibility into and confidence of quality of site-level activities

Job Responsibilities
  • Responsible for relationship building and management
  • Responsible for proactively providing local intelligence
  • Accountable for study start-up, activation, and execution to plan
  • Responsible for CRO and Study Management Interface
  • Responsible for process, standards, and oversight:
  • Protocol Site Oversight
  • Site and Study Management Interface

Qualifications / Skills

Training and Education
  • A scientific or technical degree in the healthcare area is preferred along with extensive knowledge of clinical trial methodology. In general, candidates for this job would hold the following levels of education/experience: BS/BSc/MS/MSc or equivalent + 7 years of clinical research experience and/or quality management experience.
  • Fluency in Turkish and English is required.

Prior Experience
  • Experience implementing centrally designed and developed initiatives on a local basis
  • Solid knowledge of clinical development processes with strong emphasis on monitoring
  • Demonstrated ability to oversee a 3rd party and/or demonstrated ability in Quality Assurance (preferred)
  • Site Management/Monitoring (CRA) experience
  • Project management experience preferred in the clinical development area
  • Ability to lead, troubleshoot and influence for delivery
  • Independent approach
  • This contractor position is a permanent role and provides a contract of indefinite duration.”

  • Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

    • Seniority level

      Entry level
    • Employment type

      Full-time
    • Job function

      Information Technology
    • Industries

      Pharmaceuticals


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