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The position-holder will be responsible for providing Medical leadership, support and governance of all Medical activities in the Europe Region across all Teva businesses. They...
The ClinOps Oncology Strategy & Business Operations Head will be accountable for managing a team (῀ 7-10FTEs) who are accountable for resource and capacity management,...
Develop and contribute to content, format and accountability for regulatory submissions and related supplements and amendments, regulatory documents such as meeting requests,...
This role will ensure full compliance with all local PV regulations in the region and may oversee and manage one or more PV Specialists. This PV leader will work closely with the...
Liaise with other CSO department heads and Discovery Research sub-department heads, scientists, project management, and program heads to implement and execute discovery research...
Single point of contact/single point of accountability within GRA on the Core Asset Team (CTA) and Medicines Development Team (MDT) for assigned program(s); Chairs a Global...
Provide overall medical oncology leadership for Foundation Medicine, in addition to helping shape and implement the vision and strategy for the international markets; Function as...
Oversee all activities of Medical Writing staff including hiring; project assignments; training on policies and procedures; performance review and rewards; and budget and resource...
Manages the Quality Systems organization across the EMEA region and European Centre of Operations (ECO), Kerkrade. Develops, establishes, and maintains the quality assurance...
The Manager, Biostatistical Programming completes his/her work through the development and validation of SAS software programs, macros, and utility tools. This individual prepares...
As a Medical Science Liaison, you bring the medical insight into the business and are focused on driving the scientific evidence, messages and education needed to support the...
Ensure collaboration with the global regulatory team in preparing global regulatory strategies, identifying regulatory opportunities and mitigating risks, developing competitive...
We have an exciting opportunity for a Senior Medical Manager to join the Medical Affairs Team in Spain. The individual will report to the Medical Affairs Cell Therapy TA Lead and...
This Senior Regulatory Affairs Manager will develop and lead the implementation of a robust control infrastructure and governance within Regulatory Affairs inclusive of processes,...
The Quality Assurance Lead is responsible for carrying tasks pertaining to compliance and product quality. Providing quality oversight and ensuring compliance with regulatory...
The Sr Director will provide regulatory support across the Therapeutic Areas including Infectious Diseases, Oncology, Cardiovascular and Rare diseases and, as a secondary role,...
As a Senior Research Associate/Scientist in Translational Bioanalytics, you will contribute to the delivery of data from pre-clinical animal studies to enable the progression of...
Provides expert monitoring strategy, oversight and guidance to support internal teams and sponsors. Includes defending the rationale for monitoring strategy, process and tools and...
Represent International region in Global Regulatory Teams and other cross-functional forums, for assigned development projects. Develop International regulatory strategies and...
The Head of Regulatory Affairs provides regulatory vision and leadership to the Affiliate. S/he executes these responsibilities by utilizing experience, knowledge of regulatory...
We are looking for a Regulatory Affairs Director to lead a team who thrives in a multifaceted environment, enjoys helping employees reach their potential, and encourages new...
You will manage the study start up in collaboration with PM, Regulatory Lead and, if applicable, Global Site Activation Manager (GSAM); Coordination and oversight of Critical...
The Clinical Project Manager plays an important role in the development and registration process for our products. He/she is well experienced in clinical trials and conducts...
As our new Global Patient Experience Lead you will be responsible for partnering across Galderma to champion a better future experience for people living with atopic dermatitis and...
You will have a leading role in defining the strategic quality compliance work within the CMC organization with the goal of ensuring the right level of compliance related...
We are seeking a highly motivated Scientist with a strong expertise in all aspects of biochemistry of proteins/biochemical assay design, optimization, validation, and...
The Regional Medical Director, Italy will serve as a customer facing field medical lead to the medical/scientific community and will be responsible for establishing, developing and...
In a constantly changing matrix environment amongst diverse functional teams, you will be able to leverage your strong strategic and analytical thinking, as well as your ability to...
Conduct research activities in a Therapeutic Area to expand and develop the research portfolio and build a long-term, sustainable pipeline for the Therapeutic Area, design,...
The Senior Expert Regulatory Affairs will support the development team by bringing products from research through the clinical development phases 1–3. Specifically, the position...
Leads or contributes to the strategic direction for our risk-based quality assurance program, supports and continuously improves the QM system related to GxP, manages effective...
In collaboration with project team members, defines project requirements and timelines. Organizes, creates, and maintains project plans, communicates project status to...
Within this role you will provide microbiology expertise as it relates to Drug Substance & Drug Product manufacturing. This sets the strategy for the improvement of practices and...
Represent Clinical Pharmacology in program teams and related clinical trial teams, setting-up and implement project specific Clinical Pharmacology strategies and present these to...
Work closely with the Qualified Person Responsible for Pharmacovigilance (QPPV), deputy QPPV, and other members of the pharmacovigilance team/service providers, to ensure timely,...
We are looking for a highly skilled and motivated person with previous experience from working with Quality Assurance within the Life Science sector. The person needs to be service...
The Director Global Medical Affairs Oncology (GOMA), Biomarkers & Companion Diagnostics (CDx) is a dedicated GOMA expert to partner with the GOMA Team Lead and cross-functional...
Having an overview of medicinal product safety profiles and any emerging safety concerns (e.g. via signal detection activities); Having awareness of any conditions or obligations...
The Associate Clinical Trials Regulatory Manager (CTRM) will oversee the maintenance phase of a clinical study following initial site activation through study closure. The...
Responsible for developing and executing the Clinical Development Plan (CDP) for ≥ 1 indication in an oncology development program at MorphoSys. Lead Medical Scientists and...
As (Senior) Medical Manager you have both field-based as well as office-based responsibilities. You will be key in leading field-based Medical Affairs initiatives in the...
Responsible for the local implementation of complex global regulatory strategies, obtaining and maintaining marketing authorizations for product(s) and communication of local...
This position will provide leadership, planning, direction, communication and coaching to partner with the Process Owner for GxP regulated processes in the development and...
This position reports to QC Manager, and is responsible for the management of raw material test, planning, instruction, and operations to ensure the high quality of products...
The Supply Chain Manager is responsible for managing the manufacturing of kits used in specimen collection for Laboratory Operations. The role encompasses specimen collection kit...
Ensures that all business objectives are addressed through delivering expected targets across Safety/Quality/Distribution/Cost/People (SQDCP) elements of the business; Oversees and...
Provide support and guidance to other cross functional team members on various topics in countries with regulatory framework of lower complexity or higher with support of line...
Develop Europe regulatory strategy and provide regulatory expertise within project/product teams for products under development and/or marketed products as required. Lead and...
As Head of Project Management, you will be leading a team of 5 Project Managers and act as first escalation level in the project governance structure. You are the main contact in...
As a Clinical Project Manager you will be part of the global clinical function and will be responsible for managing and coordinating clinical studies of the Cook product portfolio...
In deze nieuwe directiepositie ben je op groepsniveau samen met de CEO en CFO verantwoordelijk voor het verder uitbouwen van de organisatie. Je zorgt voor alignment van de...
The Director Supply Chain EMEA is accountable for coordinating a consensus forecast in collaboration with commercial planning, finance, and others to ensure the proper demand...
Under the guidance of the Country Manager (operational) and the Medical Director (functional), Medical Science Manager (MSM) drives the implementation of the Country medical...