شركة Certara تعلن عن 5 فرص عمل مميزة في الكويت للتقديم تابع الخطوات التالية Certara announces 5 distinguished job opportunities in Kuwait. To apply, follow the following steps:

 

Kuwait Jobs Today Certara Company announces new job opportunities. Are you looking for job opportunities in Kuwait? Certara Company announces the opening of recruitment for many jobs in various specializations in Kuwaiton today’s date. These opportunities are available to all nationalities. Learn about the available jobs and how to apply through the following advertisement. ↔️

Qualifications

• 2+ years of compliance experience in a Governance, Risk, Compliance function
• 2+ years of experience in a technical role (IT or software development) preferred in Healthcare Industry
• Basic knowledge of NIST and/or ISO standard framework
• Resourceful in an ambiguous environment
• Exceptional problem solving and communication skills
• Top notch organizational and time management skills
• Desire to continuously improve the business and one’s own knowledge
• Knowledge of current Governance, Risk and Compliance (GRC) technological tools and methodologies
• Understanding of GRC tooling and platforms, experience with Atlassian products and/or SharePoint in the delivery of documentation
• Knowledge of US and international regulations and laws related to IT-related compliance standards within the financial services industry is a plus

Qualifications

• Completion of Certara’s training and immersion programs
• MSc, PhD, PharmD, or equivalent in Pharmaceutical Sciences, Pharmacology, Toxicology, Statistics, Mathematics, or related fields. 
• A minimum of 1 to 3 years of industry/consulting experience (may be combined with academic research) working in R&D, pre-clinical and clinical environments. 
• Solid experience in pharmacometrics, clinical pharmacology, pharmacokinetics, or a related discipline in a project team setting is preferred, whether in academia or industry. 
• Expertise in PK/PD modeling with strong quantitative skills applied to develop models with nonlinear behavior, mechanistic or semi-mechanistic components relating to mechanism of action and tailored to meet specific drug-development questions. 
• Proficiency in software used for modeling analyses (e.g. Phoenix NLME, NONMEM, Adapt, Monolix) and performs dataset construction (e.g. R, SAS). 
• Independent performance of analysis and modeling and development of reports with limited supervision. 

 Skills

• Computer literate and familiar with modern communications technology.
• Familiar with Excel, PowerPoint, Word etc.
• Some familiarity with the use of search engines/PubMed etc. to find biomedical scientific data.

• Bachelor’s degree; MS or PhD preferred
• 8+ years of regulatory writing experience or equivalent experience with nonclinical sections of the CTD such as:
• 2.4 Nonclinical Overview
• 2.6 Nonclinical Summaries
• Pharmacology or Toxicology Reports
• ADME Reports

Qualifications

• BSc, MSc or equivalent in Pharmaceutical- or Life Sciences, Statistics/Mathematics/Bio-Informatics, or related fields with 1- 5 years’ experience in data management and analysis, report writing, and regulatory drug submissions.
• Advanced user of SAS software (SAS9-Base) with proven experience in life sciences and clinical trials. 
• Familiar in working with CDISC data formats. Experience with the R software platform is a plus.
• General knowledge of clinical drug development and demonstrated knowledge of pharmacokinetics and pharmacology.
• Accuracy and sense of urgency and quality, timely delivery.
• Ability to work on multiple collaborative projects, team player mentality.
• Excellent verbal and written communications skills in English.
• Eager to learn and develop.

If you’re searching for more options, you can check out a wide range of available jobs in Kuwait through this link: Kuwait Jobs.

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