Senior Global Program Safety Team Lead Job in New Jersey (NJ), Research and Development Career, Full Time Jobs in Novartis Pharmaceuticals
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Senior Global Program Safety Team Lead job in East Hanover

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Novartis Pharmaceuticals jobs
New Jersey (NJ), East Hanover
Job Code:  246490BR
Employer:  Novartis Pharmaceuticals
Category:  Research and Development
Job Type:  Full Time

Location
Country:  United States
State:  New Jersey (NJ)
City:  East Hanover
Map: 
09/05/2018

Description
Successfully serves as scientific safety leader of the Medical Safety organization to improve patients' lives and impact on overall Novartis results through robust safety evaluation expertise and medical innovation. Ensures optimal patient safety for assigned compounds, is responsible for the integration, analysis, and interpretation of internal and external safety information from all sources through lifecycle management. Provides expert safety input to the clinical development program for heavy weight/high profile projects/products. Provides guidance to assigned Medical Safety team members and builds an efficient team within the TA/DU.
Manages an efficient and successful disease area within the TA/DU Medical Safety organization, which provides robust medical and science-driven contribution to Benefit- Risk evaluation throughout product lifecycle to enable Novartis to provide impactful medicines to patients worldwide. 2. Enhances scientific and clinical experience of Medical Safety physicians / scientists through continuous training and coaching. Prepares safety objectives and evaluates and manages performance of the Medical Safety associates within the TA/DU. 3. Leads the day-to-day safety activities and provides guidance to assigned Medical Safety team members and mentee(s), as well as to the direct reports. Prepares objectives and evaluates related performance for the assigned team members 4. Mentors junior CMO and Patient Safety personnel. Proactively engages in the development of competencies across the Medical Safety Function. 5. Provides expert safety input to the clinical development program, in particular for heavy weight/high profile projects/products; is an active member of the Global Program Team (GPT), Global Clinical Team (GCT) and Clinical Trial Team (CTT). 6. Provides guidance and support to assigned Medical Safety team members. 7. Is responsible for safety issue management from formation of GPT through Life Cycle Management. 8. Develops and is responsible for key internal Novartis safety documents, reviews these documents regularly and updates as required (e.g., when significant new information received). Ensures that all project-related safety documents are consistent in safety messages. 9. Owns the safety strategy and documents it appropriately (e.g. dSPP, SSPT); leads the production of the medical safety deliverables (e.g. DSUR, PSUR, RMP) for the assigned products. 10. Is responsible for overall signal detection, monitoring, evaluation, interpretation and Sr.GPSL/Team Lead_Version 1 appropriate management of safety information, based on information from all relevant line functions, post-marketing data, and other sources. To this end, constitutes and runs the Safety Management Team (SMT). Ensures that this team appropriately and timely reviews all medical safety data from various sources (e.g. pre-clinical, clinical trial data post-marketing, literature) throughout the development and post-approval process. 11. Is responsible for documentation/tracking/record keeping of medical safety activities for the assigned compounds.Medical Degree or equivalent (preferred), PhD, PharmD or equivalent graduate level health care professional degree required. Specialty Board certification desirable. Useful additional degrees: Post gr English 5 years clinical experience postdoctoral At least 7 years progressive experience in drug development in a major pharmaceutical company (of which 5 years in a global position), including 5 years in safety at a medical position Expertise in preparing or contributing to preparation of clinical safety assessments and regulatory reports/submissions involving safety information - to include NDA submission documents Strong experience in leading cross-functional, multicultural teams Strong experience with (safety or others) issue management Strong experience in drug development, clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publications Strong leadership skills including coaching, motivating, and directing, and fostering teamwork Ability to develop and maintain effective working relationships with subordinates, superiors and peers Strong negotiation and conflict management skills Excellent written and verbal communicati
ref: (246490BR)
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