Emprego Clinical Trial Assistant Oeiras

Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Responsibilities - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF))...

A global clinical research organization is seeking a Senior Clinical Data Manager to oversee and lead clinical data management projects. This role requires a university degree and 8 years of experience, including sponsor management. The successful candidate will manage vendor contracts and ensure data quality. The position offers a competitive compensation package, with options for office or...

Job Description We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within Portugal - Zona Norte. Under the oversight of the CRA Manager, you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local regulations, our company policies and...

A leading global clinical research provider is looking for a Clinical Trial Assistant in Lisbon, Portugal. The role involves supporting Clinical Research Associates and the Regulatory and Start-Up team by managing clinical documents, assisting with compliance tracking, and preparing necessary reports. Candidates should possess a high school diploma, at least 2 years of experience in this role,...

An amazing opportunity has arisen for an Oncology Sales Representative at our company in Portugal. This position is responsible for supporting our customer‑centric business model, working with cross‑functional teams and leveraging data to identify customer needs, create a leading customer experience, and deliver better health outcomes. You will join a motivated, empathetic, and inclusive team,...

Senior Clinical Data Manager – FSP / Oncology Experience Join to apply for the Senior Clinical Data Manager – FSP / Oncology Experience role at Fortrea. 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. You will be responsible for the full cycle of Clinical Data Management queries, from...

Clinical Research Associate 2 - FSO Model - Portugal Join to apply for the Clinical Research Associate 2 - FSO Model - Portugal role at Fortrea. Job Overview Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Ensures the implementation of project plans, as assigned. Summary Of...

A leading global clinical research provider is seeking a Regulatory and Start Up Manager to oversee site activation and regulatory activities. This role requires at least 7 years of experience in scientific or clinical environments and proficiency in Portuguese for communication with the Competent Authority. The ideal candidate will possess strong negotiation and communication skills and a...

A leading global clinical research provider is seeking a Senior Psychometrician in Lisbon, Portugal. This role involves managing the psychometric evaluation of Clinical Outcome Assessment instruments used in clinical trials. The ideal candidate will possess a Master’s or PhD in a related field with extensive experience in the healthcare industry. Responsibilities include managing project...

A global clinical research organization seeks a Clinical Research Associate 2 in Portugal. Responsibilities include site monitoring, ensuring patient safety, and compliance with regulatory guidelines in clinical studies. The ideal candidate should have a degree in a health-related field, at least one year of CRA experience, and strong English communication skills. This is a full-time entry-level...

Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential Functions- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF))...

Job Description We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within Portugal - Zona Norte . Under the oversight of the CRA Manager, you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local regulations, our company policies and...

Job Description We are seeking a highly skilled Clinical Research Associate (CRA) to lead performance and compliance for assigned protocols and sites within Portugal - Zona Norte . Under the oversight of the CRA Manager, you will serve as the primary site contact throughout all phases of clinical studies, ensuring rigorous adherence to ICH/GCP, local regulations, our company policies and...

The IQVIA Dermatology Center of Excellence, a hub of Dermatology clinical innovation, is looking for exceptional Board-Certified physicians to join our team as a Medical Strategy Lead to help us expand our Dermatology portfolio and advance this dynamic and rapidly expanding area of clinical development. The Dermatology Medical Strategy Lead is a subject matter expert with experience in clinical...

Be the strategic force behind patient‑centric trial success at IQVIA At IQVIA, we are reimagining how clinical trials reach, engage, and support patients. Our Patient and Site Centric Solutions (PSCS) team partners with experts across the business to design strategies that help sponsors enroll and retain the right patients — while ensuring sites feel supported and empowered every step of the...

A leading global healthcare provider in Portugal is seeking an experienced professional to enhance patient-centric trial success. This role focuses on developing effective patient recruitment and retention strategies while leading teams in a collaborative environment. Ideal candidates will have over 10 years of experience in clinical development and strong leadership capabilities, along with...

A global clinical research firm is seeking a Senior Director, Medical Strategy Lead to drive growth in cardiovascular portfolio through innovative strategies. The ideal candidate is a Board-Certified cardiologist with at least 2 years of clinical research experience, strong communication abilities, and leadership skills. This role involves collaborating with teams for clinical trial strategies...

Senior Director, Medical Strategy Lead - Cardiologist The IQVIA Cardiovascular Center of Excellence, a hub of cardiovascular clinical innovation, is looking for an exceptional Board-Certified cardiologist to join our team as a Medical Strategy Lead to help us expand our cardiovascular portfolio and advance this dynamic and rapidly expanding area of clinical development. The Cardiovascular...

Regulatory and Start Up Manager, IQVIA MedTech, Portugal 17 hours ago Be among the first 25 applicants. Job Overview Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre‑award activities, oversight of the scope of work, budget and resources. Essential Functions - Oversee the...

The Role The Senior Psychometrician will be responsible for the on-time completion and the scientific soundness of projects or components of large, complex projects focusing on the psychometric evaluation of Clinical Outcome Assessment (COA) instruments used in clinical trials. Location Spain, Greece & Portugal Work Model Hybrid or Office based Essential Functions - Plans, organizes, and...