Duties: Author and Maintain standards and requirements for PV Ops Process and Training Team activities. Support continuous improvement activities and inspection readiness for PV Ops Process and Training Team. Support PV Ops Business Process Owners with publishing/amendment of controlled documents and conventions in Jazz LMS systems. Support PV Ops Business Process Owners with creating/amending training material in LMS, driving conventions forward and delivering training. Support PV Ops Business Process Owners with creating/amending knowledge assessments associated with training requirements. Work directly with Subject Matter Experts (SMEs) to develop these training items. Support core pre-service onboarding training for PV Ops teams and other training projects as needed to support BPOs. Provide project and operational support of the LMS within PV Ops team. Provide training/end user support for the LMS within PV Ops team. Provide coaching and mentoring to staff on a daily basis.
Education: Bachelor's degree or foreign equivalent in Business Administration, Pharmaceutical Management Studies, Pharmacy, Biology, or related field
Experience: 7 years of progressive experience in the position or related occupation
Special Requirements: Must have at least 1 year of prior work experience in each of the following:
End-to-end ICSR processing, and pharmacovigilance and clinical safety regulations and guidelines
Representing in the pharmacovigilance audits and inspections
Aggregate safety reporting, signal detection, ICSR management and Argus or other safety database systems
Leading development and management of departmental procedures and conventions
Project management in a cross-functional PV setting.
Position permits telecommuting, applicant may reside anywhere in U.S., reports to Philadelphia, PA office.
Position requires 10% domestic and international travel, fully reimbursed by employer.
Application Instructions: Email resume to apply@jazzpharma.com specifying job code 88890. EOE.