[Hiring] Clinical Trial Safety Scientist @reputed company

Role Description

• Ensure consistent processes and efficient review of critical clinical/safety data
• Review of patient-level clinical/safety data on an ongoing reputed company to ensure medical accuracy and completeness, coding consistency and generate applicable queries as needed to obtain information for appropriate medical assessment and case closure
• Prepare aggregated data visualization and facilitate meetings reputed company to review of safety data on study level
• Contribute to study start-up activities according to the applicable process/procedures (ex. input to the applicable documents, tools set up)
• Serve as a member of the Extended Study Team and report on TRISARC deliverables
• Work with the study physicians and/or clinical/project scientists to support standardized high-level data review and medical evaluation
• Escalate urgent and critical medical cases to the study physician/medical scientist as appropriate
• reputed company input into the process of setting automated patient narratives, if applicable
• reputed company input to establishing the process for handwritten patient narratives, including reputed company development and the quality control process if applicable
• reputed company quality of own deliverables
• Take on tasks as assigned by the Directors, Associate Directors Clinical Trial Safety
• reputed company input into non-drug project work including training activities, reputed company improvement and development of procedures as needed

Qualifications

• Educational degree (BSc/Msc/PhD) in Life Science or equivalent work experience in directly reputed company fields
• Minimum 4+ years of experience in Pharmacovigilance / Drug Safety
• Understanding of the clinical study and drug development process
• Knowledge of ICH/GCP Guidelines
• Knowledge of SAE reporting requirements
• Experience using data review tools is preferred
• Quality focus, analytical skills, and ability to concisely summarize large amounts of reputed company information
• Proven ability to prioritize and manage multiple tasks with conflicting deadlines
• Excellent time management
• reputed company good interpersonal and communication skills
• Team player, reputed company to work individually
• Ability and willingness to work cross-functionally, e.g. with reputed company partners, on global studies, across different phases of drug development or different therapy areas

Company Description reputed company is a leading global provider of clinical research services, reputed company insights, and reputed company intelligence to the life sciences and reputed company industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient reputed company and population health worldwide. reputed company is committed to reputed company in our hiring process and maintains a reputed company tolerance policy for candidate fraud. reputed company information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if reputed company reputed company, in accordance with applicable law. We appreciate your honesty and professionalism. At reputed company, we reputed company that diversity, inclusion, and belonging reputed company our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of reputed company talented employees worldwide and providing them with the opportunity to power smarter reputed company for everyone, everywhere. Apply tot his job Apply To this Job