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Every member of Gileads team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions and were looking for the next wave of passionate and ambitious people ready to make a direct impact.
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Job Description
Sr. Director (m/f/d) Head of Regulatory Affairs Germany
Job Responsibilities
Provides the Vision and Direction for the RA organization in Germany in line with global/regional RA Development Organization and Commercial Visions and sets clear goals and objectives in line with the Development Organization strategy
Regulatory lead on the German leadership team and ACE affiliate Regulatory core leadership team providing cross functional support and strategic advice
Ensure that Gilead fulfills all relevant requirements linked to the MA/local license as MA Holder or as local legal representative of the MA Holder for the region
Crisis management functional lead in the region
Ultimately responsible for German resource and budget planning and utilization
Lead communicator to the German Regulatory team for important changes to the local regional international and global Regulatory and Development Organization function/activities
Manages German Reg Affiliate team and leads German Regulatory activities is responsible for the German regulatory teams deliverables professional development and putting in place succession plans for critical roles
Oversees all regulatory activities in Germany acts as strategic advisor or lead on very complex or challenging issues
Advises Reg Heads on country/national scientific advice and / or pre-submission meeting preparation and follow-up challenges
Input to the International and global regulatory strategy upon request including input into clinical development programmes
Ensures compliance with local law and regulation and consistency with global procedural documents for all aspects of the German Affiliate Regulatory work
Leads or serves as a core member on local regional international and global improvements initiatives and taskforces
Expert advisor to international and local promotional material review teams
Expert advisor to local Gilead representative as required by local law e.g. Qualified Person QA QPPV Responsible Person PV RP QA etc and the respective regional functional teams
Acts as an expert to local Affiliate regional Intl or Global RA teams on German Affiliate matters
Leads risk assessments on critical or major regulatory issues and changes in Germany and develops mitigation strategies as required
A regulatory expert in updating and preparing the Company for major changes in German regulatory legislation and competitor information contributes to guideline and regulation development and develops strategies to optimize the outcome
Leads and is an ambassador for RA and the Development Organization at internal and external meetings or working parties building recognition as a thought leader
Mentoring training and coaching regulatory and non-regulatory staff
Knowledge & Skills
Expert leadership skills showing the ability to influence externally cross-functionally and within global Development Organization and RA
Excellent compelling vision and direction setting
Extensive experience working with local HA and Trade Association at a senior level
Expert in developing and implementing regulatory strategies and managing challenging discussions with the local HA
Excellent leader of complex cross functional projects and teams
Expert people management and development experience
Extensive productive cross functional internal and external networks
Expert influencer negotiator and decision maker
Excellent decision making and prioritization skills
Excellent verbal and written English language organization skills and interpersonal communication
Education & Experience
16 years of experience in RA or other relevant industry experience with BS/BA or 14 years of experience in RA or other relevant industry experience with advanced degree. Degree in a scientific field is preferred
Expert diverse knowledge and proven experience in understanding and implementing regulatory requirements in Pharmaceutical / Biotech Industry including ICH requirements and international requirements and have an understanding of current trends in the local affiliate
Expert in developing and implementing very complex regulatory strategy and managing challenging negotiations with a HA
Excellent knowledge of quality assurance promotional and non-promotional review as well as pharmacovigilance and market access
Expert in working and leading cross-functional project teams
Excellent people management experience
Expert working knowledge of country/national and regional HAs and the local Trade Associations recognized as a thought leader. Excellent knowledge of developing trends in the local rules and regulations and the potential impact to the organization
It is the policy of Gilead Sciences Inc. and its subsidiaries and affiliates (collectively Gilead or the Company) to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law all employment actions relating to issues such as compensation benefits transfers layoffs returns from layoffs company-sponsored training education assistance social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds which may include an individuals gender race color national origin ancestry religion creed physical or mental disability marital status sexual orientation medical condition veteran status and age unless such protection is prohibited by federal state municipal provincial local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
Please apply via the Internal Career Opportunities portal in Workday.
Required Experience:
Exec
Gilead Sciences is continuing to hire for all open roles. Our interview process may be conducted virtually and some roles will be asked to temporarily work from home. Over the coming weeks and months, we will be implementing a phased approach to bringing employees back to site to ensu ... View more