Empregos de team study em Lisboa

Cencora is seeking a Senior Statistical Programmer (CDISC focus) to lead CDISC data standards and programming efforts across internal and external teams. The role emphasizes SDTM/ADaM, regulatory submission readiness, and governance of CDISC datasets using SAS and R. The position requires substantial experience with regulatory components (Define.Xml, SDRG,...

Sofia, Bulgaria Lisbon, Portugal Budapest, Hungary Belgrade, Serbia Zagreb, Croatia Centurion, South Africa Prague, Czech Republic Athens, Greece Madrid, Spain Full time R1562082 Why Join Global Study Leadership? Global Study Leadership is a global, full-service team delivering clinical trials through both therapeutically aligned and...

IQVIA is seeking a global study leadership professional to oversee vendor relationships across multinational clinical trials. You will partner with Clinical Project Managers, sponsors, and cross-functional teams to ensure vendor delivery meets quality, timelines, scope and cost targets while proactively managing risks. You will lead governance activities,...

Ergomed is a specialist CRO focusing on rare disease and oncology trials, delivering complex studies with rigorous operational accountability. The Specialist, Study Start Up and Regulatory Affairs coordinates all SSU activities, ensuring regulatory compliance and acting as a key liaison between internal teams, clients, and external stakeholders. The role...

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...

Medicine moves forward here. So willyou. Ergomedis a specialist clinical research organization focused on rarediseaseand select oncology indications. We focus on the most complextrials,the studies where experience, judgement, and rigorous operational accountability make the biggest difference. We partner with small to midsize biotech companies to move...

Position:Feasibility Study Specialist I Location: Lisbon, Portugal Job Id:302-22 # of Openings:1 Feasibility Study Specialist I (Please note this role can be located in any country where CTI has a legal entity) Job Purpose / Summary Assists in analyzing and researching institutions and Investigators via CTI Feasibility Database, Data Assets and Business...

TFS HealthScience is seeking a Project Management Associate to join our clinical operations team in Portugal. You will support planning, setup, execution, and close-out of studies, maintain study documentation, CTMS records, trackers, logs, and study files, and provide administrative support to Project Managers and CRAs.This entry-level role offers growth...

Cencora is seeking a Senior Statistical Programmer (CDISC focus) to lead CDISC data standards and programming across internal and external teams, with emphasis on SDTM/ADaM and regulatory submission readiness. The role requires governance of CDISC datasets using SAS and R, plus the ability to manage multiple study data activities while driving automation and...

We are growing. And we are looking for talented people. At Decskill, we believe that technological excellence is driven by human talent. We are an IT consulting company with more than 10 years of consolidated experience in the market, focused on building long-term relationships with both our clients and our people. Today, we are a community of over 800...

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...

Job Overview The Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations, Study Management to time, cost and quality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study...

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 third‐party...

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...

Sofia, Bulgaria Madrid, Spain Belgrade, Serbia Lisbon, Portugal Budapest, Hungary Zagreb, Croatia Athens, Greece Centurion, South Africa Bucuresti, Romania Full time R1571281 Please note that, due to sponsor requirements, we will only consider candidates with experience in MASH, MASLD or Nonalcoholic Steatohepatitis. Why Join Global Study...

We’re Capital on Tap Capital on Tap started because small businesses were underserved. Big banks were slow, their products weren't fit for purpose, and small business owners often couldn't access what they needed. We set out to fix that. Today we're a financial platform - not just a credit card company. We offer a best-in-class business credit card,...

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...

IQVIA is seeking a Clinical Lead with a strong Oncology background to deliver regional and global studies from start to finish. You will oversee recruitment, site performance, quality and regulatory compliance while guiding cross‑functional teams to meet timelines and objectives. Join a global team delivering trials across diverse therapeutic areas and...

CTI Clinical Trial and Consulting Services is seeking a Clinical Data Manager to serve as the primary CDM contact. You will manage study-specific CDM documents, support data cleaning, testing, and validation, and coordinate data from external sources across CTI projects. You will also maintain project timelines, monitor data quality, and participate in...

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...