Last updated: 2025-05-18

10 Clinical Operations Management jobs in Milan.

Hiring now: Global Regulatory Affairs @ Iqvia, Clinical Research Associa @ Psi Italy, Trial Delivery Mgr Medica @ Johnson Jo, Medical Monitors @ Psicro, Medical Monitor @ Psi, Pv Mgr @ Cencora, Sr Pharmacovigilance Pv P @ Ergomed.Explore more at at kaamvaam.com

šŸ”„ Skills

clinical development (3) project management (3) clinical trials (3) pharmacovigilance (3) GCP (2) budget management (2) safety monitoring (2) medical review (2) regulatory compliance (2) signal detection (2)

šŸ“ Locations

Milan (10)

Iqvia

Skills & Focus: Global Regulatory Strategy, Health Authorities, regulatory lead, NDA/MAA/Extensions/Variations filings, compliance activities, GMP, GCP, project timelines, multicultural environment, clinical development
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Around 3 years' experience in Regulatory Affairs
Type: Full time
Benefits: Competitive salary package, Permanent contract
Skills & Focus: Clinical Project Manager, pharmaceutical, CRO, project management, clinical studies, SOPs, clinical operations, budget management, eTMF, study registration
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: At least 5 years of experience in a similar position in a pharmaceutical company or CRO
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Psi Italy

Skills & Focus: Clinical Research Associate, monitoring visits, study startup, CRF review, source document verification, query resolution, site communication, internal project teams, feasibility research, audits and inspections
Type: Hybrid

Johnson & Johnson

Skills & Focus: Clinical Trials, Project Management, Vendor Management, Healthcare, Regulatory Compliance, Team Leadership, Risk Management, Operational Strategy, Clinical Research, Training
About the Company: A leading company in healthcare innovation dedicated to building a world where complex diseases are prevented, treated, and cured.
Experience: Minimum of 4 years clinical trial experience in Pharmaceutical, Healthcare or related industries.
Type: Hybrid

Psicro

Skills & Focus: medical monitoring, clinical data, safety monitoring, SAE reports, clinical documents, medical review, clinical data analysis, patient safety, clinical development, medical training

Iqvia

Skills & Focus: contract negotiation, clinical research, contract management, budget templates, proposal development, clinical trials, investigator grants, compliance, financial contracting, team collaboration
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 2 to 5 years relevant sponsor or clinical research organization clinical site contracting experience.
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Psi

Skills & Focus: clinical trials, GCP guidelines, medical advice, data analysis, safety monitoring, pharmacovigilance, regulatory compliance, clinical development, risk mitigation, medical data review
About the Company: PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and…

Cencora

Skills & Focus: pharmacovigilance, local ICSR Management, signal detection, PSUR / RMP submission, risk minimization measures, training and support, team management, communication skills, legislative guidelines, project management
About the Company: Cencora is an innovative company focused on creating healthier futures for people and animals. They prioritize employee responsibility in achieving their purpo…
Experience: Several years’ experience and profound knowledge in the field of pharmacovigilance
Type: Part time
Benefits: Benefits offerings vary by country and are aligned with local market practices; eligibility and effective date may diff…

Ergomed

Skills & Focus: pharmacovigilance, medical review, risk management, safety reports, signal detection, adverse events, literature screening, regulatory authority, benefit-risk assessment, training

Iqvia

Skills & Focus: clinical trials, GCP, regulatory compliance, project management, leadership, budget management, stakeholder collaboration, training, Italian regulations, clinical research associates
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: A minimum of 5 years of clinical operations experience in the pharmaceutical, biotech, or medical device industry, with at least 2 years in a managerial capacity.
Type: Full time
Benefits: Competitive salary package, commensurate with experience.