Senior Pharmacovigilance Project Manager- Europe
ՀեռավարԲոլոր աշխատատեղերը Sofia-ում (99)Բոլոր «Ծրագրի ղեկավար» աշխատատեղերը (692)Լրիվ դրույք
Բաց է նաև՝ BulgariaUnited KingdomBucharest
Ergomed is seeking a Senior Pharmacovigilance Project Manager to work remotely in Europe. This role involves serving as the main point of contact for project-related issues, ensuring client satisfaction with the services provided by PrimeVigilance. Responsibilities include preparing project scopes based on client agreements, planning project activities with deadlines and milestones, and generating reports for clients and management. Candidates should have a proven background in pharmacovigilance, including experience with individual case safety reports (ICSRs), aggregate report writing, literature screening, and standard operating procedure (SOP) preparation. A background in project management within a service provider or contract research organization (CRO) is preferred. Applicants should hold a degree in a health-related field or life sciences and possess strong communication skills for engaging with senior professionals in pharmaceutical companies. Leadership qualities such as planning, mentoring, and problem-solving are essential. This position is ideal for individuals who thrive in a collaborative environment and are committed to delivering quality outcomes in patient safety.
Acting as the primary contact point for project-related matters
Managing client’s expectations to make sure the client is satisfied with services of PrimeVigilance, and that the work PrimeVigilance delivers meets, or even exceeds, the clients’ expectations.
Preparing project scope and objectives based on the signed agreement between the client and PrimeVigilance.
Project activities planning, including deadlines and interim milestones
Reporting for the client and the PrimeVigilance management, e.g., preparation of Monthly reports, serving as basis for invoicing.
Proven track record of demonstrated Pharmacovigilance activities including processing and quality review of ICSRs, writing, or contributing to aggregate reports, literature screening, reconciliation, and preparation of SOPs
PV Project Management experience from ideally a service provide / CRO
Health Care Professional or Life Science Graduate
Be comfortable with communicating at senior levels within pharmaceutical organizations
Have good leadership qualities including skills in planning, mentoring, meeting facilitation, communication and problem solving.
When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.
We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here.
Quality: we hold ourselves to the standard patients deserve.
Integrity and trust: we do the right thing, especially when it is hard.
Drive and passion: we care about the outcome, because someone is waiting on it.
Agility and responsiveness: we move quickly, because patients cannot wait.
Belonging: everyone is welcome, and every voice counts.
Collaborative partnerships: we go further by going together.
We look forward to welcoming your application.
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