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Accountable for the execution of clinical studies, or assigned portion of clinical studies, per contract while optimizing speed, quality and cost of delivery and ensuring...
Pharmacovigilance Project Manager is responsible for assuring compliance with local Quality Management System, delegating tasks employees delegated on the project, overseeing...
Provide expert medical/scientific advice for assigned products and related therapeutic areas, including responding to requests for scientific/technical information; contribute to...
Maintain robust collaboration/interaction with the in-country partner functions, to carry out and monitor local PV activities, in compliance with PV regulatory requirements and...
The Director will help to set direction for clients in the coordination, execution, guidance and implementation of regulatory programs, requirements and compliance activities. The...
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures...
This role will be instrumental in helping us coordinate activities and programs within Medical Study Operations, including Investigator-Initiated Studies Programs for respiratory...
You will guide regulatory strategy to provide direction for planning and coordinating activities related to product regulatory (biologicals, chemical drugs and medical devices),...
The key responsibilities of this role will be to build, develop and maintain relationships with Key Opinion Leaders, engaging them on their fields of interest and on areas of...
As a Clinical Project Manager II, you will be responsible for managing the clinical projects and ensuring the quality of the services in accordance with contractual obligations,...
As CHC Global Quality Process Manager, you will be accountable for define, analyze, improve processes in the clinical environment to fulfill consumers/subjects needs as well as...
Define and lead the global policy and strategy for Teva Patient Safety Pharmacovigilance for the PV quality management system, as described above; Oversee and maintain Teva's...
As a Director, Global Pharmacovigilance - Safety Physician you will be part of the Global Pharmacovigilance (PV) and Medical Scientific Unit (MSU) supporting drug safety across the...
The Director Global Medical Affairs Oncology (GMA), ADC, under the direction of the Senior Director, GMA Oncology ADC (Global Medical Affairs team lead for compound), is...
Designs and executes evidence generation activities (non-interventional, pragmatic, low-interventional and interventional Phase IIIb/IV studies) that will fill priority evidence...
You will be a key intermediary between our Penzberg Team and the broader Foundation Medicine Team in the USA. You will facilitate the study intake process with...
As quality assurance partner collaborates with internal and external stakeholders to ensure appropriate GCP and GVP processes are implemented and maintained. Provides day-to-day...
We are recruiting for an Associate Director, Regulatory Affairs UK&IE to have the ownership for all new UK (UK/GB/NI) and IE Marketing Authorisation submissions for New...
As the Associate Medical Director, you will provide medical, clinical, and scientific advisory expertise to all IQVIA divisions as requested. Participating in all aspects of...