Vagas na Fortrea em Portugal

Senior Regulatory Medical Writer needed to author complex regulatory documents, including Clinical Study Reports and Protocols, with a minimum of 4 years of experience. Role involves interpreting study data into clear language and collaboration across Europe. ...

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

A leading pharmaceutical company is seeking a Regulatory Affairs Specialist in Portugal to oversee submissions and ensure compliance with regulations. The ideal candidate will have a Bachelor's degree in Life Sciences or equivalent and a minimum of 3 years of experience in the Ph ...

The Senior Clinical Data Manager role is a great opportunity to work within our sponsor dedicated department and have this unique relationship with a sponsor. · ...

A leading biopharmaceutical solutions organization is seeking a Senior Medical Writer. This role involves managing medical writing deliverables, ensuring accuracy, and adhering to regulatory standards. The ideal candidate will have 3-5 years of experience in regulatory writing wi ...

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 · ...

A leading pharma company is seeking a Senior Regulatory Medical Writer to take the lead in authoring complex regulatory documents. This full-time, permanent position requires a minimum of 4 years of regulatory writing experience, including significant experience with Clinical Stu ...

Job Overview: · Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. · Summary of Responsibilities: · Respo ...

A leading pharma company is seeking a Senior Regulatory Medical Writer to take the lead in authoring complex regulatory documents. This full-time, permanent position requires a minimum of 4 years of regulatory writing experience, including significant experience with Clinical Stu ...

+ 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 · ...