PositionVollzeit · Festanstellung · Lead · Gesundheitswesen
KonditionenHybrid
VergütungExpected Annual Base Salary Range for role: 169,400 – 314,600 CHF
Anforderungen7+ J. Erfahrung · Doktortitel · EU/EFTA-Bewilligung
Deine Übereinstimmung
01
Skills
02
Process safety managementRegulatory Compliance in MedicineCross-Functional LeadershipGlobal Medical StrategyMulticultural Team CollaborationTechnical leadershipPublic safety education
Sprachen
Englisch
Vergütung
03
Expected Annual Base Salary Range for role: 169,400 – 314,600 CHF
Die Stelle
04
01Manage an efficient and successful disease area within the CRM Therapeutic Area (TA)/Development Unit (DU) Medical Safety organization.
02Enhance scientific and clinical experience of Medical Safety physicians / scientists through continuous training and coaching.
03Prepares safety objectives and evaluates and manages performance of the Medical Safety associates within the TA/DU.
04Identifies talents and high potential associates and is able to defend and discuss in front of leadership team.
05Provide expert safety input to the clinical development program for assigned projects/products.
06Responsible for safety issue management from formation of Global Program Team (GPT) through Life Cycle Management.
07Responsible for overall signal detection, monitoring, evaluation, interpretation and appropriate management of safety information.
08Responsible for documentation/tracking/record keeping of the assigned compounds medical safety activities.
09Leading the preparation of the safety strategy for health authority responses.
10Contribute to and often leading the development of departmental and functional/business unit goals and objective.
Anforderungen
↳Medical Degree or equivalent (preferred), PhD, PharmD or equivalent graduate level health care professional degree required.
↳Minimum 5 years clinical experience postdoctoral.
↳At least 7 years progressive experience in drug development in a major pharmaceutical company.
↳Solid expertise in preparing or contributing to preparation of clinical safety assessments and regulatory reports/submissions.
↳Substantial experience in leading cross-functional, multicultural teams.
↳Strong experience with (safety or others) issue management.
↳Extensive experience in drug development, clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publication.
↳Strong leadership skills including coaching; motivating and directing and fostering teamwork.
Vorteile
＋In addition to your base salary, you may be eligible for a performance-based bonus depending on certain performance parameters.
＋We also offer a variety of competitive benefits in kind to help you thrive personally and professionally.
＋Flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave.
