Senior/ Director Clinical Safety Pharmacovigilance at Innovent Biologics in Sonoma, California

Posted in Other about 18 hours ago.

Type: full-time





Job Description:

This role will lead the clinical safety pharmacovigilance (PV) activities within expected scope and timelines. The incumbent will play a major role in ensuring the safety pharmacovigilance deliverables and processes are followed and support the establishment and growth of PV functions to assure global capabilities and execution.

Key Roles & Responsibilities
  • Lead clinical safety pharmacovigilance in conducting safety surveillance of assigned products.
  • Prepare and manage the aggregate reports draft, finalization and submission timelines by working closely with CROs and relevant department contributors.
  • Draft the safety sections of aggregate reports, IB, protocols, health authority responses, data management or safety management committee presentations and other similar activities.
  • Accountable for the delivery of assigned tasks according to quality, time, budgets, and resources.
  • Liaise with case processing team internally and CROs to ensure timely delivery of all case processing and health authorities' commitments for PV safety.
  • Partner with pharmacovigilance operations, clinical development and operations, regulatory and other functional areas for the successful implementation and execution of all PV commitments.
  • Act as a safety pharmacovigilance resource in interactions with internal and external stakeholders.

Role Requirements
  • MD (or an equivalent level of professional, clinical and/or scientific education, training and experience) required.
  • Experience in pharmaceutical or biotech industry working with Phase I - III clinical trials, experience in Oncology safety surveillance is highly desired.
  • Experience working with safety databases such as Argus, ArisG, Oracle or equivalent.
  • Clinical experience as practicing physician post residency training for 2-3 years is desirable.
  • More than 6-8 years' experience in safety pharmacovigilance in bio/pharmaceutical industry.
  • Extensive experience in leading the preparation of periodic aggregate safety reports; deep understanding of signal detection and management in pre and post market setting is essential.
  • Independent, self-motivated individual with a highly entrepreneurial style coupled with self-confidence and a positive management style.
  • Ability to manage multiple projects in a fast-paced environment with global teams in different time zones.
  • Excellent organizational communication and coordination skills.
  • Good interpersonal and ownership.

More jobs in Sonoma, California

Health Care
about 5 hours ago

Sonoma Post Acute
Health Care
about 5 hours ago

Sonoma Post Acute
Other
about 12 hours ago

Partnology
More jobs in Other

Other
less than a minute ago

Horizontal Talent
Other
less than a minute ago

Horizontal Talent
Other
less than a minute ago

Horizontal Talent