Clinical Research Associate II ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion
Forvia, a sustainable mobility technology leader We pioneer technology for mobility experience that matter to people. Your mission, roles and responsibilities The intern will support the Industrial Program team in all activities related to the industrialization
IQVIA is growing! Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider) and Traditional (Sponsor-Agnostic) delivery models. Apply now and have your resume considered for Lead Data Manager opportunities across multiple teams
Do You Want to Work in a Safe, Inclusive, and Equitable Environment? Will You Be Part of a Company Committed To Crafting a Brighter Future For Us All? Are you ready to Build a Career with
Job Overview: Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports). Manage
CRA II, Multisponsor Remote PORTUGAL 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
Freelance Site Activation Specialist – Portugal (Home-Based) Location: Portugal (home-based) Contract type: Freelance FTE: 0.75 - 1.0 /full time Start: immediately Duration: around 4 month About the Role We are looking for a Freelance Site Activation
Site Enrollment and Engagement Leads collaborate with research staff and other stakeholders to drive trial recruitment and support study-specific training needs. The role as a strategic partner to both external and internal stakeholders to optimize the site
What Youll Do: Assist in organizing, composing, and producing professional letters, summaries, reports, minutes, etc, using Microsoft Office software including Word, Access, and Excel Proofread documents ensuring grammar, spelling, and punctuation are correct Assist in developing
What Youll Do: Provide first-level support to all CTI employees for computer system hardware, software, and telecommunications Procure and install all new electronic devices such as PCs; set up as required Meet with all new employees
Join us on our exciting journey! IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. IQVIA offers a broad range of solutions
Tech Systems/Support Analyst Lisbon, Portugal Remote/Home-based Full Time The Tech/System Analyst provides first-level support to Clinical Trials personnel via phone, email, and chat, ensuring timely resolution of technical and operational inquiries. Essential Functions: • Processes and provides
What Youll Do: As the lead Biostatistician on the studies assigned, perform the following tasks: Act as primary statistical contact for internal and external project team members. Communicate and work with Biostatistics management to maintain the
Product Marketing Manager Department: Marketing Employment Type: Full Time Location: Portugal - Porto Description Emergn is a technology and management consultancy with a mission to set our clients free. No dependency. No short-term fix. Just teaching
Sponsor-dedicated. Full time. Remote in the UK, Spain, South Africa, Greece, Portugal or Hungary. We are on a mission to deliver solutions that bring life-changing treatments to patients faster. But we can´t do it alone. We
Job Overview: Manage ‘Client’ or ‘Project’ specific PSS operations associated with products including the entire adverse events process: which may include safety data collected from clinical trials and/or post marketing setting (i.e., unsolicited reports) for specified projects.
What Youll Do: Assist in compilation and revision of Regulatory Affairs (RA) documents required for clinical trials submissions Assist in the contact with local study teams for RA documents collection and checks, when applicable Assist in contacting
What Youll Do: Support the administration and maintenance of financial systems, including Sage Intacct, Concur, and Certinia (FinancialForce) Assist with maintaining resource records, user access, roles, and permissions in compliance with internal controls and audit requirements.
PROPOSAL & CONTRACT MANAGER SPAIN/PORTUGAL (home-based) 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
Clinical Research Associate I Home based Portugal ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration,