Remote Pharmaceuticals Jobs • Europe

The Staff Toxicologist will play a critical role in authoring and guiding toxicological risk assessments for medical devices and combination products. This position involves performing high-level biological safety evaluations, providing strategic input on regulatory submissions, and mentoring junior staff members as needed. The Staff Toxicologist will ensure the safety and compliance of products.

This role supports the NQPPV Network Lead to fulfil the legal requirements to ensure oversight of AbbVie’s PV system and ensures that National QPPVs (NQPPVs) meet their legal obligations worldwide. The role is the linchpin to a strong & experienced NQPPV Network. Key responsibilities include acting as the primary point of contact for all European NQPPVs.

As the project physician, you'll provide medical and scientific expertise to project teams, focusing on data accuracy and patient safety. You'll participate in the strategic planning and execution of critical development programs for clients in Haematology and Oncology, while also supporting Business Development efforts. Responsibilities include preparing medical considerations for proposals, writing scientific content, collaborating on regulatory strategies, and serving as a medical resource for study sites.

The Associate Director provides medical and scientific strategic and operational input into core medical affairs activities including health-care professional and provider interactions, generation of clinical and scientific data, internal and external educational initiatives, and safeguarding patient safety. This position works closely with commercial teams to provide strategic medical input into core brand strategies, marketing activities and market access.

This role integrates efforts in creating and implementing a medical proposition that sets AbbVie apart and unifies the portfolio, benefiting therapeutic areas and geographic regions. The position supports the rheumatology strategy, accelerating transitions and maintaining a portfolio mindset as new assets, diseases, and approaches are integrated. The goal is to establish AbbVie as a leader capable of addressing diverse patient profiles, conditions, and disease manifestations.

We are looking for motivated CRAs based in the Paris/Ile-de-France area to join our sponsor dedicated CRA team! As a Clinical Research Associate, you will be fully dedicated to one of our global pharmaceutical clients focused on oncology studies.

The Senior Manager Patient Recruitment role serves as the critical link between patients, advocacy groups, and internal clinical teams to ensure that the patient voice is integrated throughout the clinical trial lifecycle. You will be building and maintaining relationships with global and regional patient advocacy groups and individual patient representatives. You will act as the primary point of contact for patient organizations related to clinical trial education and collaboration.

As a CRA, you will monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas. You will collaborate with the team, developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely. As the first point of contact for study sites, escalating any concerns/issues to other departments.

This position serves as an expert in Study Start Up (SSU) activities and strategy including the use of various clinical systems (e.g. CTMS) to enable consistent and compliant forecasting and data collection. Manage and may lead the day-to-day operations within Study Start Up to ensure completion per established goals and objectives in compliance with applicable GCP/ICH guidelines and other regulatory requirements.