Regulatory and Start Up Specialist

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. At least 3 years' experience with submissions and...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. At least 3 years' experience with submissions and...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. At least 3 years' experience with submissions and...

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. At least 3 years' experience with submissions and...

The Position:Step into the shoes of a Junior Regulatory Specialist, where you'll become the mastermind behind the orchestration and execution of regional regulatory documents on an as-needed basis. You'll find yourself at the heart of global and local interactions, nurturing harmony and collaboration like a true diplomat.But that's not all You'll also dive...

**Regulatory Affairs Specialist - European Union** Clinglobal is an Animal Health Contract Research Organisation and supports our global operations in various countries. We are currently looking for a** Regulatory Affairs Specialist** based in the EU to join our growing Regulatory Affairs team at Clinglobal. This position offers the opportunity to work...

Company DescriptionFounded in 1997 by two Medical Doctors, Ergomed Plc is dedicated to the development of new drugs to save or improve lives. Operating with a global footprint in over 55 countries, Ergomed has the expertise to manage even the most challenging clinical trials. Ergomed provides services to over 100 clients in a range of therapy areas but...

**The Position**: Are you passionate about the pharmaceutical industry and eager to make a significant impact? We are seeking a dedicated and innovative Regional Regulatory Specialist to join our team. In this role, you will have the opportunity to leverage cutting-edge technology to coordinate and streamline the processing of crucial regulatory documents....

Study Start Up Associate II At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation:...

Company Description Founded in 1997 by two Medical Doctors, Ergomed Plc is dedicated to the development of new drugs to save or improve lives. Operating with a global footprint in over 55 countries, Ergomed has the expertise to manage even the most challenging clinical trials. Ergomed provides services to over 100 clients in a range of therapy areas but...

Company Description We are PrimeVigilance (part of Ergomed PLC), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs...

**The Position**: Step into the shoes of a Junior Regulatory Specialist, where you'll become the mastermind behind the orchestration and execution of regional regulatory documents on an as-needed basis. You'll find yourself at the heart of global and local interactions, nurturing harmony and collaboration like a true diplomat. But that's not all! You'll...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery,...

Germany Finance Group FunctionsJob Reference #BRCity Frankfurt am MainJob Type Full TimeYour role Do you want to play a key role in improving the effectiveness of Regulatory Reporting processes? Are you an analytic thinker, selfdriven and a strong team player? We're looking for someone to help us:prepare an appropriate and timely delivery of regulatory...

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration,...

IQVIA currently offers the exciting opportunity as experienced Study Start-Up Specialist / Site Activation Specialist (m/w/d) to work in the Country Site Activation Department in our Frankfurt office or in home office throughout Germany. In this role you will perform tasks at a country level associated with clinical research site activation activities in...

Germany - Finance - Group Functions **Job Reference #** - 276543BR **City** - Frankfurt am Main **Job Type** - Full Time **Your role** - Do you want to play a key role in improving the effectiveness of Regulatory Reporting processes? Are you an analytic thinker, self-driven and a strong team player? - We're looking for someone to help us: - prepare an...

Study Start Up Associate II At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation:...

Study Start Up Associate II At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation:...

Trilogy Writing & Consulting GmbH, an Indegene Company, is a specialized medical writing company that prepares regulatory documentation for the international pharmaceutical industry. We have a hybrid or in-office vacancy in our German office (Frankfurt, DE) for an: **Associate Marketing and Communications Specialist (w/m/d)** We are looking for an outgoing...