Empregos de team study em Porto

About this roleTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full-service capabilities, resourcing, and Functional Service (FSP) solutions.TheSite Coordinatoris responsible...

At IQVIA, our Project Vendor Managers play a critical role in the successful delivery of global clinical trials. Working at the intersection of project leadership, vendor strategy and study execution, you'll partner with sponsors, third-party providers and cross-functional teams to ensure vendor services are delivered efficiently, compliantly and with a...

IQVIA is seeking a Design & Implementation Lead for Study Hub, responsible for end‑to‑end technical design, configuration, and integration readiness across decentralized and hybrid trials. You will translate complex protocol requirements into robust technical specifications and drive multi‑system integration with sponsors, IQVIA teams, and...

IQVIA is seeking a Design & Implementation Lead for Study Hub, responsible for end‑to‑end technical design, configuration, and integration readiness across decentralized and hybrid trials. You will translate complex protocol requirements into robust technical specifications and drive multi‑system integration with sponsors, IQVIA teams, and...

Due to sponsor requirements, only candidates with a strong Oncology background will be considered for the role Why Join Global Study Leadership?Global Study Leadership is a global, full-service team delivering clinical trials through both therapeutically aligned and customer-dedicated delivery models. You'll work across a diverse portfolio including...

Description Senior Medical Writer - Europe / home based - FSP Team Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate...

Due to sponsor requirements, only candidates with a strong Oncology background will be considered for the role Why Join Global Study Leadership?Global Study Leadership is a global, full-service team delivering clinical trials through both therapeutically aligned and customer-dedicated delivery models. You'll work across a diverse portfolio including...

Alimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational excellence, and deep therapeutic expertise, including supporting more than 70% of IBD compounds in development. We operate as a private,...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Freelance Senior Clinical Research...

MoonLake Immunotherapeutics in Porto, Portugal seeks a Manager Quality (GCP) on a fixed-term contract to lead GCP quality oversight across clinical programmes and support audits, CAPAs and inspections readiness. You will collaborate with CROs and internal teams to ensure trials meet regulatory standards. Key responsibilities include maintaining the QMS,...

Customer Success Manager - Real World Evidence (UK) Get AI-powered advice on this job and more exclusive features. About The Company What’s Promptly in a nutshell Promptly is building the first patient-centered global evidence network, offering real world data sharing and monetization capabilities. Together with a selected network of Partners, we...

SimpleStudy is seeking a senior product designer to shape the end-to-end user experience for its consumer AI study platform. You’ll work with Oisin and a founding designer to define product direction,roadmap priorities, and design philosophy across mobile and web. You’ll own onboarding, retention, and growth features in a PLG environment, defend your...

CIIMAR in Porto, Portugal is seeking a Junior Researcher for the X-IAS project to study cumulative effects of multiple invasive species in estuarine ecosystems. You will join the Benthic Ecology and Environmental Solutions team and contribute to field sampling, biodiversity assessments, lab analyses, mesocosm experiments, modelling, data analysis and...

As a Senior Biostatistician you will provide statistical leadership throughout the clinical trial lifecycle—from protocol development and study design through analysis, interpretation, and regulatory documentation. For assigned studies, you will shape the statistical strategy, including endpoints, estimands, sample size, randomization, and risk-based...

Renvolt in Porto, Portugal is seeking an Automation & Control Engineer to join our growing team on a fixed-term contract. You will study requirements for monitoring and control systems, design architectures, and prepare technical specifications. The role involves on-site verification, coordinating with subcontractors, and exploring advanced solutions for...

IQVIA is seeking a full-time Clinical Research Associate (CRA) in Porto Salvo, Portugal. The role covers site initiation, monitoring and close-out visits, plus supporting subject recruitment planning and regulatory compliance per GCP/ICH guidelines. You will track regulatory submissions, recruitment, CRF completion and data query resolutions while...

Join an exciting oncology study and use your clinical research expertise to support accurate data management and successful trial delivery. R&D Partners is seeking a Clinical Research Coordinator for a part-time freelance role in Portugal. This is an exciting opportunity to contribute to oncology clinical research in the healthcare sector. The role requires...

Astrum CRO is seeking a Regulatory Affairs & Pharmacovigilance Manager to lead the RA/PV team across clinical trials and client projects.You will ensure regulatory compliance and patient-safety systems, oversee submissions, safety reporting, and sign-off on key study documents.Ideal candidates hold a degree in pharmacy, medicine, or life sciences, with...

Company SimpleStudy is a consumer AI platform for students. We help them stay motivated to study their subjects - everything from Biology and Mathematics to Literature and Art. Our small team has already helped +1.5 M students worldwide (UK, Ireland, Brazil, South Africa, and Australia) study better, and ~40–50k new students join us every week. We are a...

Job Purpose The Manager Quality (GCP) ensures robust GCP compliance and quality oversight across MoonLake´s clinical development programmes by serving as a quality expert, leading and supporting audits, managing quality risks, and supporting inspections readiness. The role provides operational quality support to clinical teams and vendors to ensure trials...