Salario promedio: $26.937 /por mes
Más estadísticasResultados de la búsqueda: 9 vacantes
$102,600 - $178,600 por año
...organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to... ...substantial business value.
JOB RESPONSIBILITIES
- Design and develop optimization models to improve business processes...
$102,600 - $178,600 por año
...organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to... ...to collaborate with our expert data science team, leading the design, implementation, and optimization of machine learning systems...
...• Reviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are... ...with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients...
...successful candidate will be responsible for designing, developing, and maintaining Oracle... ...functional teams to analyze requirements, design efficient database structures, write... ...FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites...
...successful candidate will be responsible for designing, developing, integrating, and... ...functional teams to analyze requirements, design efficient integration solutions, database... ...FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites...
...electronic data capture requirements
• May perform investigational product (IP) inventory, reconciliation and reviews storage and security... ...of local requirements for real world late phase study designs
o Chart abstraction activities and data collection
o...
...Submissions Specialist - Follows the project direction provided by the designated country
start-up advisor (CSA) and SSUL. May serve as a... ...94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial...
...review for safety, drug coding, maintenance of drug dictionary, and MedDRA coding as required.
Validation and Submission of xEVMPD product records, including appropriate coding of indication terms using MedDRA.
Manual recoding of un-recoded product and substance...
...advising clients on laws, regulations, and industry standards governing clinical development and commercialization of pharmaceutical products.
Job Responsibilities:
• Responsible for providing legal regulatory advice and counsel on global regulatory and clinical...
