Empleos: pharmacovigilance

Job DescriptionAn amazing opportunity has arisen for a Drug Safety Associate Director, Pharmacovigilance (PV) within International Pharmacovigilance (IPV). This position plays a critical role in overseeing local PV processes and day-to-day adverse event case management across ex-US markets, ensuring adherence to applicable regulations, company policies, and...

BandLevel 5Job Description SummaryJoin Novartis and make a profound impact on patient safetyAs our Medical Safety Lead in our Cardio Renal Metabolic team, you'll spearhead safety evaluations, collaborate with dynamic global teams, and craft safety strategies that not only protect patients but also drive groundbreaking medical innovation. Be a part of...

What you will be doingJob DescriptionCencora Pharmalex is one of the leading service providers for the Pharmaceutical Industry globally and is specialized in all aspects of drugs and medical devices approval, of the market development and any action of effective product maintenance. The success of our company resides in the expert knowledge and high...

Company Description PSI is a leading Contract Research Organization with 30 years experience in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description PSI Medical Monitors provide medical input...

Safety & PV Specialist I ** Hybrid SPAIN **Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.  Our Clinical Development model brings the customer and the patient...

Job title: Expert Medical Regulatory WriterLocation: Barcelona% of travel expected: Travel required as per business needJob type: Permanent and Full timeAbout The JobOur Team:Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General...

Grupo Ferrer InternacionalAt Ferrer we use business to fight for social justice. We have long been a company that looks to do things differently; instead of maximizing shareholder returns, we reinvest much of our profit in initiatives that give back to society. Back where it belongs. We go beyond compliance and are guided by the highest standards of...

Job description:1. FUNCTIONAL CONTENTMain RoleThe Regulatory Affairs Specialist will be responsible for managing the regulatory lifecycle of US FDA-approved products, ensuring ongoing compliance and supporting regulatory activities for the ongoing new product development projects.This role requires close collaboration with cross-functional teams including...

Are you a Pharmaceutical Affairs/Regulatory/Quality specialist looking to take the next step into a role with real responsibility and impact? Do you want to ensure the quality and safety of medicines while working in a fast-growing global biotech company?Ascendis Pharmais a global, fast-growing biopharmaceutical company driven by our core values:Patients,...

Primary work location: Spain | Scope: Spain & ItalyTheLead Commercial Quality Southensures that commercial distribution activities are conducted in full compliance with EU Good Distribution Practice (GDP) and EU Good Pharmacovigilance Practice (GVP), while supporting business growth through pragmatic, risk-based governance in the Southern European...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions.Join Our Team as a Medical AdvisorAbout this roleAs part of...

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals...

Scientist – Biologics & Advanced Therapies (Quality Control)Shift: Afternoon only (13:30–21:30)OverviewA growing life sciences organisation is seeking a Scientist to join its Biologics & Advanced Therapies Quality Control team. This role focuses on analytical method development and validation for complex biologics, including monoclonal...

CRA I ** Hybrid MADRID or BARCELONA**Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center...

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are...

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities...

Job title: Expert Medical Regulatory WriterLocation: Barcelona% of travel expected: Travel required as per business needJob type: Permanent and Full timeAbout the jobOur Team:Sanofi Business Operations is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General...

Job title: Principal Medical Regulatory WriterLocation: Barcelona% of travel expected: Travel required as per business needJob type: Permanent and Full timeAbout the jobOur Team:Sanofi Global Hub is an internal Sanofi resource organization based in India and is setup to centralize processes and activities to support Specialty Care, Vaccines, General...

We are currently looking for an experiencedSafety Physicianto support ongoing and upcoming clinical development projects. This role requires a highly competent professional with strong expertise acrossClinical Safety and Pharmacovigilance, contributing both operationally and strategically.Key responsibilities will include:Providing comprehensive safety...

Key ResponsibilitiesDevelop relationships within specialized healthcare environments, with the aim of providing accurate information to the medical community about the company's products and strategy.Map and develop the assigned territory in a critical and analytical manner, identifying market needs and opportunities.Manage relationships with key...