Parma PV & Clinical Trials Operations Lead (Hybrid)

Biopharma Careers; Parma; Ibrido; EUR 41.000 - 51.000; Tempo pieno

Vantaggi offerti da questo lavoro

Pension

Private medical insurance

Wellbeing programme

Flexible benefits programme

Relocation support

Descrizione del lavoro

Chiesi Research & Development is seeking a Pharmacovigilance professional to lead PV OPS activities for interventional clinical trials. Based at the Parma headquarters with a flexible hybrid setup, you will ensure safety data collection, compliance and cross‑functional collaboration across the R&D organization.

The role requires a Master’s degree in a relevant field, 4+ years in pharma/biotech R&D with 3+ years in PV or clinical research, and fluent English for an international environment.

Competenze

• Master degree in science, medicine, biology, pharmacy or related fields.
• Minimum 4 years of experience in R&D within Pharmaceutical and/or Biotechnology industry, with at least 3 years of experience in Pharmacovigilance or Clinical Research.
• Fluent English and ability to operate in an international environment.

Mansioni

• Support the PV OPS CT Head in ensuring PV requirements are integrated into processes and documented in procedures.
• Ensure strategic collection, assessment and delivery of high‑quality clinical trial safety data to agencies.
• Actively engage CT customers, affiliates and other stakeholders.
• Participate in interdepartmental meetings inside and outside R&D.
• Act as owner for specific PV processes, including training, procedure maintenance and vendor oversight.
• Provide training of internal and vendor staff for PV processes.
• Oversee PV operations activities with CROs and ensure data in the PSMF is properly filled.
• Open deviations related to PV activities and contribute to CAPA plans.

Conoscenze

Pharmacovigilance

Clinical Trials

Regulatory compliance

Communication skills

Team collaboration

Problem solving

Formazione

Master's degree in science/related field

Descrizione del lavoro

Chiesi Research & Development is seeking a Pharmacovigilance professional to lead PV OPS activities for interventional clinical trials. Based at the Parma headquarters with a flexible hybrid setup, you will ensure safety data collection, compliance and cross‑functional collaboration across the R&D organization.

The role requires a Master’s degree in a relevant field, 4+ years in pharma/biotech R&D with 3+ years in PV or clinical research, and fluent English for an international environment.