Last updated: 2025-05-12

10 Biopharmaceutical Leadership jobs in Rome.

Hiring now: Sr Analyst Customs Trade @ Baxter, Medical Ops Regulatory Jr @ Abbvie, Developing Medical Expert @ Iqvia, Medical Advisor @ Blueprint , Qualified Person For Phar @ Client, Milestone One Site Coordi @ Psicro, Pv Officer @ Primevigil, Head Of European Local Op @ Johnson Jo.Explore more at jobswithgpt.com. at kaamvaam.com

🔥 Skills

clinical trials (3) Regulatory (2) medical affairs (2) Supply Chain (1) Customs (1) Trade Compliance (1) EMEA (1) Healthcare (1) Medical Products (1) International Trade (1)

📍 Locations

Rome (9) Latina (1)

Baxter

Skills & Focus: Supply Chain, Customs, Trade Compliance, EMEA, Healthcare, Medical Products, Regulatory, International Trade, Logistics, Innovation
About the Company: Baxter is a global healthcare company, dedicated to saving and sustaining lives through innovative medical products and services.
Type: Full time
Benefits: Comprehensive benefits options reflecting the value placed in employees.

Abbvie

Skills & Focus: medical operations, regulatory manager, clinical studies agreements, field support, ethical aspects, clinical research, compassionate uses, health care professionals, archiving, interaction
About the Company: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tom…
Experience: At least 6 months of previous experience in regulatory and ethical aspects pertaining to clinical research.
Type: Full-time

Iqvia

Skills & Focus: Ophthalmology, medical strategy, stakeholder management, multichannel campaigns, evidence generation, budget management, clinical trials, medical affairs, analytical skills, network building
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: Preferable 3+ years of professional experience in the medical/pharmaceutical field as a Medical/Scientific Advisor or Medical Science Liaison or in other Medical Department’s roles
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.
Skills & Focus: Medical Science Liaison, scientific exchanges, Thought Leaders, educational activities, medical education programs, data generation, collaborations, scientific presentations, clinical study results, healthcare professionals
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 2 years experience as an MSL
Type: Full time
Benefits: Benefits programs designed to meet total well-being needs.

Abbvie

Skills & Focus: Medical Operations, Regulatory, Clinical Studies, Agreements, Clinical research, Compassionate Uses, Health Care Professionals, Ethical, Matrix context, IIS activities
About the Company: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tom…
Experience: At least 6 months of previous experience in regulatory and ethical aspects pertaining to clinical research.
Type: Full-time

Blueprint Medicines

Skills & Focus: Medical Advisor, KOL management, clinical trial data, medical affairs, oncology, hematology, regulatory requirements, scientific publications, strategic prioritization, cross-functional collaboration
About the Company: Blueprint Medicines is a global, fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solvi…
Experience: 3+ years of experience in the biotech or pharmaceutical industry in a similar role
Type: Full-time

Client

Skills & Focus: Pharmacovigilance, ICSRs, SAE, safety assessment, Risk Management Plans, regulatory requests, signal detection, benefit-risk assessment, adverse event, clinical trials

Psicro

Skills & Focus: Clinical Study, ICH-GCP, Feasibility, Monitoring Visits, Patient Enrollment, Data Entry, Adverse Events, Regulatory Documents, Contract Negotiations, Study Procedures
Type: Part-time

Primevigilance

Skills & Focus: case processing, Individual Case Safety Reports, SAE Management, SUSAR Management, clinical trials, healthcare, pharmacovigilance, mentoring, training, database outputs
Experience: Several years in case processing

Johnson & Johnson

Skills & Focus: Regulatory Affairs, Innovative Medicine, Leadership, Talent Development, Strategic Alignment, Submissions, Compliance, Business Support, Patient Access, Team Management
About the Company: Johnson & Johnson is a company dedicated to health care innovation, empowering the development of treatments that are smarter and less invasive with a focus on…
Type: Hybrid