...Role
Position Title: Senior Statistical Programmer
About the role: Senior Statistical... ...programmers as Trial Programmer for phase I to IV clinical studies or assigned project-level... ...knowledge of programming software (e.g. SAS) as well as industry requirements (e.g. CDISC...
About the Role
Clinical Project Manager
Location – Hyderabad #LI Hybrid
About the Role:
This role is responsible to Lead and manage a multidisciplinary cross functional Clinical Trial Team (CTT) (medical writing, statistics, data management, monitoring partner, drug...
...Position Title: Principal Statistical Programmer
About the role: Principal Statistical... ...the production of statistical outputs for clinical study reports, publications, and market promotions... ...of programming languages (e.g., SAS and R).
• Manage the outsourcing of programming...
...collected and in alignment with the protocol.
• Support the assessment of new data collection requirements in assigned studies and provide clinical input into the development of new and updated clinical Data Standards (for CRFs as well as 3rd party data collection methodologies)...
...maintenance or in closeout phase or ongoing studies post primary database lock with the oversight of the LCTL/CTL, as assigned. Support the clinical protocol development process in collaboration with the CTL/Lead CTL and the Clinical program Leader (CPL): chip in to the development...
About the Role
Job Purpose
The Head of Operational Excellence, Clinical Development will be accountable for leading key strategic global operational excellence activities across the CD function. The role will support strategic planning and operational execution in partnership...
...About the role
“150! Clinical scientific experts, globally, are part of Global Drug Development (GDD) team, working to ensure clinical trial data and regulatory reports are of highest quality throughout the life cycle of each program, across all disease areas. Be part of...
...Global Drug Development (GDD) organizations to apply the scientific knowledge of pharmacokinetics, pharmacodynamics, metabolism and clinical pharmacology in advancing the drug candidates from discovery and clinical development through approval and beyond. Novartis portfolio...
...About the role
Clinical Data Scientist
Location – Hyderabad/ Mumbai
About the Role:
Provide timely and professional ongoing management of Data Management deliverables and of clinical trial data with respect to cost, quality and timelines for all assigned trials...
About the Role
Your responsibilities will include, but are not limited to:
• Represents GCS as a core member in the integrated Clinical Trial Team (iCTT); defines and advises the iCTT on the optimal clinical trial supply strategy in terms of, but not limited to, packaging...
...details : Channelsoft IT services Pvt LtdÂ
Domain: Health Care (Clinical Trails)
About Channelsoft
Channel Soft is a pioneer in... ...university , Vijayawada .
Responsibilities For Clinical SAS Programmer:
• Creating and executing SAS edit check programs
• Validating...
...operational, for one or more assigned trials in collaboration with the clinical trial team. May support project level deliverables for a... ...skills. Proficiency in use of statistical software packages (e.g. SAS, R). Knowledge of drug development and Health Authority guidelines...
..., listings and figures for Interventional and Non-Interventional Clinical studies.
Maintain efficient interfaces with other statisticians... ...to deliver objectives.
•Excellent knowledge of/experience with SAS/ R/ Splus or any other business or research analytic software...
...experience in a closely related field within the pharma industry (e.g., clinical research, statistics, epidemiology, pricing).
• Master’s degree... ...tools and statistical programming languages such as SAS, R, R/shiny, Tableau, Spotfire, SPSS, STATA, WinBUGs.
• Deep knowledge...
...Lead projects in the development of programming routines (such as SAS or R) along with sophisticated SQL queries to extract, clean,... ...• Bachelor’s degree or equivalent experience plus 8+ years as programmer or data scientist in the pharma industry, contract research organization...
...and Learning
KA : Karnataka
RA : Rainforest Alliance
RA SAS : Rainforest Alliance Sustainable Agriculture Standard
SLM : Sustainable... ...TOR : Terms of Reference
UNEP : United Nations Environment Programme
Project Overview
The project seeks to address two...
...Industry
Experience with building analysis solutions and using analytics / BI packages desirable (e.g. Tableau, ACL, Business Objects, SAS, MicroStrategy, Spotfire, QlikView)
Skills/ Knowledge:
Deep understanding and appreciation of the internal control environment...
...such as I2C, IPMB, PMBUS, SPI, LPC, UART, JTAG.
7) Experience with one or more of the following standards/technologies: SCSI, SES, RAID, SAS, SATA, SSD, SMART, PCI Express, HBA, network protocol TCP/UDP, etc is a plus.
8) Experience with PSoC or MCU firmware development is a...
About the Role
Responsible for contributing to the planning, coordination, development and timely delivery of high quality Clinical submission documents to Regulatory Affairs (RA) for
1) New Drug Applications (NDA), Biologic Licensing Applications (BLA), Marketing Authorization...
...relevant work instructions incl. financial risk controls (NFCM)
• Provide process/system expert support & training to all countries having clinical trial activities – Governance over RDF CoE future transitions, KPIs, projects, check-in NFCM controls.
• Support audit reporting...
...Independently manage and execute drug shipment ticket review process (US)
• In addition to regulatory manager, provide guidance to clinical functions on regulatory compliance activities, such as requirements for TOOs, VDRs, drug shipment etc.
• Assist regulatory managers...
...inclusion sur nos lieux d’implantation, dans le respect des Objectifs de Développement Durable de l’ONU.
Ce recrutement fait partie du programme Jeunes Talents Vicat et constitue une première étape dans votre parcours au sein du Groupe.
Description de la mission
- Participer...
...Responsibilities: Development Data Team is responsible to design and execute data management strategy across Drug Development line functions i.e. Clinical Operations, Clinical Data Standards, Technical Research & Development, Regulatory Affairs and Patient Safety. Function also...
About the Role
Your responsibilities include, but are not limited to:
• Provides scientific and medical expertise on assigned clinical projects. Contributes to clinical strategy for the Asian region.
• Accountable for all aspects related to wind down projects including...
...work environment and diverse teams representative of the patients and communities we serve.
Role Requirements
• 8 years relevant clinical trial operations experience, from technology or health care sector. General understanding of drug development – early development, clinical...
...tools that optimize the acquisition, storage, integration, mining, analysis, visualization, and interpretation of chemical, biological, clinical and operational data.
Key Responsibilities:
• Develop state-of-the-art software tools and methodologies to support the discovery...
...majeur regroupant les activités de ciment, granulats, béton, et sac, avec six entités juridiques.
Ce recrutement fait partie du programme Jeunes Talents Vicat et constitue une première étape dans votre parcours au sein du Groupe.
Description de la mission
En tant que...
...mission to bring innovative medicines to patients worldwide. You will collaborate with colleagues from Statistics, Data Management and Clinical Development and have the opportunity to analyze data and derive key messaging to secure approvals from Health Authorities. Read on...
...leading expert level knowledge on innovative medicine domains and capabilities (including patient services, cell and gene therapies, clinical and medical).
• Accountability for understanding the technical components of strategic platforms and their associated integrations....
...partners and cross-functional teams to solve critical business problems. Understand life science data sources including preclinical, clinical, sales, contracting, promotions, social media, patient claims and Real-World Evidence
• Research and co-develop with supervisor in...