Drug Safety Scientist

Keyrus Life Science is looking for a Drug Safety Scientist who will ensure the safety of all clinical trials participants and patients administered through the assigned products by collecting and reporting of all safety data (adverse events).

The Drug Safety Scientist ensures that case processing activities are aligned with company’s standards and that regulatory timelines are achieved. This is done by liaising with global stakeholders (both internal and external). Within this interaction, you will ensure that all documentation and processes are in place to achieve successful recording and reporting of safety data during the clinical trial phases and the entire life cycle of a product.

In this Drug Safety Scientist position, you will have a relevant liaison-related oversight to the higher management and drive the understanding of adverse event collection requirements across all business units. Moreover, you will contribute to the advancement of new processes and methodologies.

Profile

• Scientific background (pharmaceutical, biomedical sciences or similar)
• Prior experience (1 to 3 years) in pharmacovigilance / drug safety
• Knowledge of Good Clinical Practices (GCP)
• Knowledge of Good Pharmacovigilance Practices (GVP)
• Experience working with clinical safety documentation, reporting of adverse  events from clinical trials, local regulatory requirements, and pharmacovigilance methodology
• You have good project management skills 
• General understanding of worldwide regulatory requirements

• Fluency in English and French

You are open to change and have excellent coordination abilities. In your day to day work you are attentive to details, but can demonstrate pragmatism where appropriate.

What we offer

At Keyrus, thanks to the expertise of our people and external partners, each employee is welcomed with a varied integration program. You will join a dynamic and international environment with enthusiastic and professional colleagues.

We invest considerable time and resources in training our staff (technical and non-technical courses) to continuously support you in your personal and professional growth. On top of this, you will receive a complete salary package including attractive extra-legal benefits (company car, petrol card, meal vouchers, group insurance, hospitalization…) based on your background and experience.

Who we are

Keyrus Life Science is an international Consulting, Contract Research Organisation and Functional Services provider with a reputation for transparency and integrity, highly focused on being able to deliver with excellence. Our ‘human’ approach to service provision is what differentiates us from our competitors. Combined with our high caliber staff, this approach has allowed us to become a key player in clinical research.

At Keyrus Life Science we’re proud of our commitment to delivering services of the highest quality, not only skillfully, efficiently and reliably, but also with sincerity and genuine care for our clients’ projects, priorities and reputation. Thus we maintain and advance our vision and our standards, all the while ensuring that we serve your interests better

From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information, Real World evidence services.