Clinical Research Associate Jobs in Spain, Latest Clinical Research Associate Jobs in Spain

Allucent is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Allucent is a non-laboratory environment. At Allucent, our mission is to help bring new therapies to light.When you work at Allucent, that means rolling up your sleeves and

Allucent is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Allucent is a non-laboratory environment. At Allucent, our mission is to help bring new therapies to light. When you work at Allucent, that means rolling up your sleeves and

Allucent is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Allucent is a non-laboratory environment. At Allucent, our mission is to help bring new therapies to light. When you work at Allucent, that means rolling up your sleeves and

Allucent is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Allucent is a non-laboratory environment. At Allucent, our mission is to help bring new therapies to light.When you work at Allucent, that means rolling up your sleeves an

Allucent is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Allucent is a non-laboratory environment. At Allucent, our mission is to help bring new therapies to light.When you work at Allucent, that means rolling up your sleeves and

CATO SMS and Pharm-Olam, LLC have merged to form Allucent!Allucent is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Allucent is a non-laboratory environment. At Allucent, our mission is to help bring new therapies to light.When you

TFS HealthScience is excited to be expanding our SRSteam and we are looking for an experienced, highly motivated CRA who shares our vision of providing clinical research excellence. Our SRS team is a highly experienced international group of professionals led by an industry expert.We are a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. We combine the full-service capa

As a member of our clinical research team, you will participate in the execution of clinical studies to assess the safety and effectiveness of Penumbra’s products. Working from your REMOTE HOME OFFICE, you will work with confidential patient and company data, interfacing with internal and external stakeholders, managing and monitoring clinical trials in the area of neurovascular therapies for stroke, aneurysm and/or pulmonary embolism. All candidates need to reside within an hour of a major ai

General SummaryAssists in the planning, design, and execution of clinical studies to assess safety and effectiveness of products. This position works with confidential patient and company data, and interfaces with a variety of internal and external stakeholders. Specific Duties and Responsibilities•Participate in the monitoring functions in a clinical study including site management, qualification, initiation, routine monitoring, and final close out.*•Assist Clinical team with the development,

As a member of our clinical research team, you will participate in the execution of clinical studies to assess the safety and effectiveness of Penumbra’s products. Working from your REMOTE HOME OFFICE, you will work with confidential patient and company data, interfacing with internal and external stakeholders, managing and monitoring clinical trials in the area of neurovascular therapies for stroke, aneurysm and/or pulmonary embolism. All candidates need to reside within an hour of a major ai

Responsibilities:Monitor on-site and remotely clinical trials in accordance with TFS and/or client company Standard Operating Procedures, FDA regulations, and GCP and ICH guidelinesReview CRFs (paper or electronic) and subject source documentation for validity and accuracy and generate queries to investigational sites/clients to resolve problem dataIdentify site problems/deficiencies and bring to the attention of management through trip reporting, memos, and verbal communication with Project Man

Key Responsibilities Monitor on-site and remotely clinical trials in accordance with TFS and/or client company Standard Operating Procedures, FDA regulations, and GCP and ICH guidelinesReview CRFs (paper or electronic) and subject source documentation for validity and accuracy and generate queries to investigational sites/clients to resolve problem dataIdentify site problems/deficiencies and bring to the attention of management through trip reporting, memos, and verbal communication with Projec

Responsibilities:Monitor on-site and remotely clinical trials in accordance with TFS and/or client company Standard Operating Procedures, FDA regulations, and GCP and ICH guidelinesReview CRFs (paper or electronic) and subject source documentation for validity and accuracy and generate queries to investigational sites/clients to resolve problem dataIdentify site problems/deficiencies and bring to the attention of management through trip reporting, memos, and verbal communication with Project M

As an experienced member of our clinical research team, you will support the Clinical Study Manager and participate in the execution of clinical studies to assess the safety and effectiveness of Penumbra’s products. Working with confidential patient and company data, you will interface with internal and external stakeholders, managing and monitoring clinical trials in the area of neurovascular or peripheral vascular therapies.The job- Provide leadership and guidance to Clinical Research team. -

Responsibilities:Monitor on-site and remotely clinical trials in accordance with TFS and/or client company Standard Operating Procedures, FDA regulations, and GCP and ICH guidelinesReview CRFs (paper or electronic) and subject source documentation for validity and accuracy and generate queries to investigational sites/clients to resolve problem dataIdentify site problems/deficiencies and bring to the attention of management through trip reporting, memos, and verbal communication with Project Man

Responsibilities:Monitor on-site and remotely clinical trials in accordance with TFS and/or client company Standard Operating Procedures, FDA regulations, and GCP and ICH guidelinesReview CRFs (paper or electronic) and subject source documentation for validity and accuracy and generate queries to investigational sites/clients to resolve problem dataIdentify site problems/deficiencies and bring to the attention of management through trip reporting, memos, and verbal communication with Project Man

Responsibilities:Monitor on-site and remotely clinical trials in accordance with TFS and/or client company Standard Operating Procedures, FDA regulations, and GCP and ICH guidelinesReview CRFs (paper or electronic) and subject source documentation for validity and accuracy and generate queries to investigational sites/clients to resolve problem dataIdentify site problems/deficiencies and bring to the attention of management through trip reporting, memos, and verbal communication with Project Man

Responsibilities:Monitor on-site and remotely clinical trials in accordance with TFS and/or client company Standard Operating Procedures, FDA regulations, and GCP and ICH guidelinesReview CRFs (paper or electronic) and subject source documentation for validity and accuracy and generate queries to investigational sites/clients to resolve problem dataIdentify site problems/deficiencies and bring to the attention of management through trip reporting, memos, and verbal communication with Project Man

Responsibilities:Monitor on-site and remotely clinical trials in accordance with TFS and/or client company Standard Operating Procedures, FDA regulations, and GCP and ICH guidelinesReview CRFs (paper or electronic) and subject source documentation for validity and accuracy and generate queries to investigational sites/clients to resolve problem dataIdentify site problems/deficiencies and bring to the attention of management through trip reporting, memos, and verbal communication with Project M

Responsibilities:Monitor on-site and remotely clinical trials in accordance with TFS and/or client company Standard Operating Procedures, FDA regulations, and GCP and ICH guidelinesReview CRFs (paper or electronic) and subject source documentation for validity and accuracy and generate queries to investigational sites/clients to resolve problem dataIdentify site problems/deficiencies and bring to the attention of management through trip reporting, memos, and verbal communication with Project M