TRABAJO REGULATORY AFFAIRS CLINICAL WRITING BARCELONA, BARCELONA
(27 ofertas de trabajo)
Listado de trabajos de Regulatory affairs clinical writing en Barcelona, Barcelona
Regulatory affairs management director, regulatory science & execution
Position: regulatory affairs management director (rad), regulatory science & execution, global regulatory affairs location: barcelona - spain (3 days working from...
Associate director, business analyst, ddit dev., regulatory affairs
Experience in regulatory affairs business processes is a plus (e... we are looking for an experienced individual in global drug development regulatory affairs to...
Associate director, clinical development scientist
Represent the clinical study team at the clinical sub team... engage with clinical investigators on clinical studies to enable quality clinical execution, analyze...
Broad background of experience working in pharmaceutical business and prior experience in several areas within regulatory affairs... accountabilities provide ongoing...
The clinical research associate (cra) is responsible for managing clinical studies at assigned sites and serves as the primary contact with study sites...
Data and algorithm development engineer
Prepare regulatory documentation and design processes with the quality and regulatory affairs teams to comply with the artificial intelligence regulation and other...
Global development medical director
Work closely with colleagues in other functions including patient safety, regulatory affairs, and clinical operations... you will provide support for medical monitoring...
Data and algorithm development engineer, barcelona
Pre-process process and analyze data from clinical trials including demographic clinical and device usability data... prepare regulatory documentation and design...
Senior study start up associate
Strong understanding of regulatory requirements and guidelines for clinical trials, including ich-gcp and local regulatory requirements... in addition to your competitive...
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Prepare and present findings from real-world evidence studies to internal and external stakeholders, including scientific conferences, ministries of health, regulatory...
You will work closely with study implementation teams, as well as clinical operations, data management and regulatory affairs to ensure the solutions meet the requirements...
Business process document manager
Location: barcelona (on site) join our clinical operations team within the biopharma business unit, where we are responsible for delivering clinical studies...
Provide medical / scientific support to com in the conduction of (global and local) clinical studies as well as in the determination of clinical trial centers and...
Associate director, senior patient safety scientist oncology
regulatory reports, health authority responses and the safety content of marketing authorisation applications... your ability to work collaboratively will facilitate...
Support creation and implementation of medical plans develop a strong business acumen, to be a key strategic business partner to the organisation in conjunction...
Associate director, medical communications and information
• collaborate with key stakeholders, including medical affairs and other partner functions... • stay abreast with the latest changes and trends in the therapeutic...
Research editor, companies ownership research, risk & compliance data
Job description: about the role dow jones risk & compliance is a global provider of third-party risk management and regulatory compliance solutions...
Research editor, italian and french, adverse media entities
Job description: job title: research editor, italian and french, adverse media entities about the role dow jones risk & compliance is a global provider of third-party...
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