Job Title: Drug Safety Specialist
Location: Upper Gwynedd, PA- Hybrid Role (2 days/week onsite).
Duration: 12 months+
Note: 1 year assignment. Hybrid assignment(2 days/week onsite). Work Location: Upper Gwynedd, PA.
We are looking for Contractors to support PV Operations and Global Process Enablement in Documentation and Training and PV Quality and Compliance with responsibilities to include:
Documentation, training, and global standards team within Client in need of a supportive and highly motivated individual within their team that will assist in developing and maintaining documents outlining the processes to ensure high quality individual case and aggregate safety ing in accordance with pharmacovigilance (PV) policy and regulations.
Assist in the management and maintenance of PV-controlled documents (e.g. Global Safety Database User Manual, Standard Operating Procedures, and training material).
Assist in the authoring, reviewing and implementation of new PV-controlled SOPs and supportive documents.
Assist in reviewing, creating, and delivering trainings.
Process incoming communications from internal and external sources and initiate appropriate course of action and/or response.
Perform quality review of expedited and periodic s to ensure adherence to global case processing standards and regulatory requirements.
Monitor group mailboxes utilized for the centralization of process/subject specific inquiries.
Qualification:
Education: Bachelor’s degree or Master’s degree or Advance level degree in a life science/healthcare/pharmaceutical related field.
Required:
Software:
MS office suite
Veeva Vault is preferred.
Personality:
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