Clinical Research Associate 2 - Oeiras

A Nova SBE procura um/a Senior Research Associate para trabalhar em estreita colaboração com o Diretor Académico na promoção da missão da instituição. · Nesta função, você será fundamental para o avanço da gestão de projetos, coordenação de investigação e desenvolvimento de conte ...

Clinical Research Associate · Your Responsibilities Will Include · Performing site selection, initiation, monitoring and close-out visits · Supporting the development of a subject recruitment plan · Evaluating the quality and integrity of site practices in accordance with regulat ...

Senior Clinical Research Associate · Your Responsibilities Will Include · Performing site selection, initiation, monitoring and close-out visits · Supporting the development of a subject recruitment plan · Evaluating the quality and integrity of site practices in accordance with ...

Site monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. · Valid Driver's License · ...

Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. · ...

+ Site monitoring and site management responsibility for clinical studies according to Company, · and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. · Qualifications (Minimum Required)University or college degree · BASIC KNOWLEDGE OF REGULATORY GUIDELINES · ...

Support market research on trends, emerging ingredients, and consumer preferences in the supplements industry. Assist in the formulation and creation of new food supplement products. · ...

The role involves supporting market research on trends and consumer preferences in the supplements industry. · ...

We're seeking a Clinical Research Associate II to join our team in designing clinical trials, interpreting medical data, and advancing innovative treatments. · Conducting site qualification visits for clinical trials. · Ensuring protocol compliance and patient safety. · ...

· Company Description · PSI is a leading Contract Research Organization with almost 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees.  We focus on delivering quality and on-time services across a variety of thera ...

Clinical Research Associate · Your responsibilities will include: · Performing site selection, initiation, monitoring and close-out visits · Supporting the development of a subject recruitment plan · Evaluating the quality and integrity of site practices in accordance with regul ...

We have a team of over 500 talented people and more than 40 different nationalities, diverse areas of expertise and professional experience that are shaping the future of healthcare. · Support brand planning and performance rhythms for RDBU by preparing inputs for monthly monitor ...

This is your chance to explore a world of opportunities at AMGEN's office in Lisbon's city center, fostering innovation, excellence, and inspiration. · ...

The Clinical Trial Assistant 2 will perform daily administrative activities to ensure a complete and accurate Trial Master File delivery.Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents a ...

Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems. · ...

Country Activation and Submissions representative for IQVIA in Portugal. Key tasks include site activation, document collection, submissions and negotiations. · ...

We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within Portugal - Zona Norte. · We keep the patient at the very heart of all that we do and strive to find solutions and treatments for some of th ...

This Analyst will participate in developing and delivering consulting projects for German headquarters clients and affiliates. · Candidate should have excellent analytical skills, data-driven, and experienced with large data sets. Should be able to work collaboratively with Germa ...

This is a fully-home based role available across most of the European Countries.IQVIA is a leading global provider of advanced analytics, · technology solutions and clinical research services to the life sciences industry. · ...

We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within Portugal - Zona Norte. The CRA will serve as the primary site contact throughout all phases of clinical studies. · Build and sustain strong ...