Associate Director, Clinical Regulatory
vor 7 Monaten
**Associate Director, Clinical Regulatory**
Denali Therapeutics is dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine.
**The Opportunity**
**Responsibilities**
- Accountable for developing and implementing regulatory strategy for complex development programs
- Leads project teams in implementing and delivering the regulatory strategy across multiple programs/indications and/or programs of increasing complexity
- Responsible for proactively identifying regulatory risk and mitigation plans in support of clinical development plans
- Accountable for overseeing and directly leading global Health Authority interactions
- Participates in cross-functional teams, providing regulatory feedback and support
- Partners with external vendors in support of regulatory document preparation and submission
- Maintains up-to-date knowledge of the regulatory landscape, regulations, and guidelines. Proactively assesses and communicates impact, potential risks, and potential mitigations
- Leads and executes non-project regulatory activities
**Requirements**:
- Bachelor's degree required. Advanced degree in life sciences strongly preferred.
- 6+ years or equivalent relevant experience in regulatory affairs
- Thorough understanding of drug development process and the pharmaceutical industry and healthcare environment including regulatory requirements and policy trends
- Strong regulatory experience with INDs/CTAs, NDAs/BLAs/MAAs, lifecycle management, interactions with Health Authorities, developing and implementing regulatory strategies with a proven track record of significant regulatory accomplishments.
- Broad strategic skill set, including creativity and effectiveness in identifying and addressing major strategic challenges (e.g., competitive landscape, challenging therapeutic areas).
- Skilled in influencing, partnership, and collaboration, including demonstrated ability to deliver on goals within a cross-functional team/partnership environment with a high level of professionalism
- Excellent written and verbal communication skills
- Strong ability to prioritize workload
- Well-prepared, competent, and confident when interacting with senior management, health authorities, and internal and external partners
- Able to prospectively identify potential problems and to partner effectively and positively to solve issues
Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class.
**Applicant Privacy Policy**
LI-SC1
-
Associate Director, Global Regulatory Affairs Cmc
vor 6 Monaten
Zurich, Schweiz Takeda Pharmaceutical VollzeitAre you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as an Associate Director, Global Regulatory Affairs CMC - Marketed Products in our Zurich office. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As an...
-
Associate Director
vor 1 Woche
Zurich, Schweiz Takeda Pharmaceutical VollzeitJob Description **People First** - At Takeda we are dedicated to improving the health and well-being of all people and bringing them the hope of a brighter future. It is our passion that transforms every job into meaningful action. **Our people are the heart of Takeda**. Looking for an interesting role where you can develop your career, work at a growing...
-
Associate Director, Global Regulatory Affairs Cmc
vor 7 Monaten
Zurich, Schweiz Takeda Pharmaceutical VollzeitAre you looking for a patient-focused company that will inspire you and support your career? If so, be empowered to take charge of your future at Takeda. Join us as an Associate Director, Global Regulatory Affairs CMC - Marketed Products in our Zurich office. Here, everyone matters and you will be a vital contributor to our inspiring, bold mission. As an...
-
Associate Director Regulatory Affairs, Marketed
vor 7 Monaten
Zurich, Schweiz Takeda Pharmaceutical VollzeitAre you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as an **Associate Director, EUCAN (Europe & Canada) Regulatory Affairs **Strategy Lead, Marketed Products **in our **Zurich** office. **Here, you will be a vital contributor to our inspiring, bold mission.** **OBJECTIVE**: -...
-
Clinical Director, Clinical Research
vor 8 Monaten
Zurich, Schweiz MSD VollzeitWe are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we ‘follow the science’ and that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference...
-
Associate Director Global Regulatory Affairs Cmc
vor 7 Monaten
Zurich, Schweiz Takeda VollzeitJoin Takeda as Associate Director, Global Regulatory Affairs CMC Established Products Inspired Collaboration (EPIC) Lead, where you are accountable for developing and executing on GRA CMC strategies for lifecycle management. You ensure global strategies are implemented across existing portfolio, while ensuring team effectiveness in a complex matrix...
-
Associate Regulatory Reporting, Bank
vor 7 Monaten
Zurich, Schweiz coni+partner AG VollzeitOur client is the headquarters of a bank in Zurich. We are looking for an accounting specialist (m, f, d) as a Associate Regulatory Reporting - Bank Aufgaben Responsible for regulatory reporting requirements related to national and international transactions for HQ, subsidiaries and private and corporate clients / Responsible for managing day-to-day...
-
Zurich, Schweiz Takeda Pharmaceutical VollzeitAre you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine?Join us as a **Director Global Regulatory Affairs, Rare Genetics and Hematology - Gene Therapy** to be based in, based in either Zurich, Switzerland or Cambridge, Massachusetts, USA. **Here, you will be a vital contributor to our inspiring, bold...
-
Associate Director/ Director, Eucan Regulatory
Vor 5 Tagen
Zurich, Schweiz Takeda Pharmaceutical VollzeitAre you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine? Join us as a ** Director, EUCAN Regulatory Lead, Oncology** in Zurich, Switzerland. **Here, you will be a vital contributor to our inspiring, bold mission.** **Objective**: - Defines, develops and leads regional strategies to maximize regulatory...
-
Zurich, Schweiz Veeva Systems VollzeitVeeva is a mission-driven organization that aspires to help our customers in Life Sciences and Regulated industries bring their products to market, faster. We are shaped by our values: Do the Right Thing, Customer Success, Employee Success, and Speed. Our teams develop transformative cloud software, services, consulting, and data to make our customers more...
-
Clinical Research Associate Ii
Vor 4 Tagen
Zurich, Schweiz Clinipace Vollzeit**Job Title**:Clinical Research Associate II **Job Location**:Zurich, Switzerland (Home-based in Switzerland) **Job Overview**: **Job Duties and Responsibilities**: - Provides support to Project Team and Clinical Operations Team. - Maintains working knowledge of protocols and Monitoring Plans for assigned projects. - Demonstrates strong written and verbal...
-
Clinical Research Associate Ii
vor 9 Stunden
Zurich, Schweiz Clinipace Vollzeit**Job Title**:Clinical Research Associate II **Job Location**:Zurich, Switzerland (Home-based in Switzerland)** **Job Overview**: **Job Duties and Responsibilities**: - Provides support to Project Team and Clinical Operations Team. - Maintains working knowledge of protocols and Monitoring Plans for assigned projects. - Demonstrates strong written and...
-
Clinical Trial Associate
Vor 7 Tagen
Zurich, Schweiz Proclinical VollzeitA Mid-sized Pharma are recruiting for an experienced Clinical Trial Associate to join their growing on a 6 month contract with option to become a permanent employee after the initial assignment. This is a great opportunity to join a busy clinical team working across a variety of highly complex trials whilst taking on a wide range of responsibilities. The...
-
Associate Director Ra Instrumentation
Vor 7 Tagen
Zurich, Schweiz Tecan Vollzeit**Join Tecan! Join the market leader!** **Work in an international and dynamic environment, share our success!** Do you want to make a significant difference in how the world is looking tomorrow and contribute to the innovation of state-of-the-art, cutting-edge technology products? Then look no further and join our Quality & Regulatory team at Männedorf,...
-
Eucan Regulatory Manager
Vor 7 Tagen
Zurich, Schweiz Takeda Pharmaceutical VollzeitAre you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine?Join us as a **EUCAN Regulatory Manager - Clinical Trials** in Zurich. **Here, you will be a vital contributor to our inspiring, bold mission.** Under supervision from a senior team member and/or in collaboration with EUCAN Regulatory Lead: -...
-
Manager, Clinical Trial Regulatory Lead
vor 7 Monaten
Zurich, Schweiz Takeda Pharmaceutical VollzeitOur team is growing and for this we need bright minds with creativity and flexibility - **what talent do you have?** - Objective / Purpose_:_ _ - Executes or oversees all activities related to the creation, submission, and maintenance of CTAs Globally (GEM and EUCAN region), in Europe through the EU Clinical Trial Information System (CTIS) or legacy...
-
Associate Director Epidemiology
vor 7 Monaten
Zurich, Schweiz Takeda Pharmaceutical Vollzeit**People First** - At Takeda we are dedicated to improving the health and well-being of all people and bringing them the hope of a brighter future. It is our passion that transforms every job into meaningful action. **Our people are the heart of Takeda.** **OBJECTIVE** The purpose of this position is to provide strategic epidemiology and risk management...
-
Director Regulatory Affairs
vor 7 Monaten
Zurich, Schweiz Sonova VollzeitWho we are You enjoy creating and innovating. You never stop striving for better. You take responsibility and you get results. You love being part of a team. Above all, you want your work to matter: Welcome to our world! At Sonova we create sense by bringing sound to life. Our innovative hearing care solutions help millions of people enjoy life’s...
-
Associate Director, Gcp Compliance Lead, Deviation
vor 7 Monaten
Zurich, Schweiz Takeda Pharmaceutical Vollzeit**About** the role**: As the Associate Director, GCP Compliance Lead, Deviation Management, Clinical Quality Assurance, you will establish standards for excellence in GCP investigation documentation, root cause analysis, responses, CAPAs, and effectiveness checks to optimize effective and consistent performance within Research and Development, Plasma Derived...
-
Associate Director, Gcp Compliance Lead, Deviation
vor 7 Monaten
Zurich, Schweiz Takeda Vollzeit**About** the role**: As the Associate Director, GCP Compliance Lead, Deviation Management, Clinical Quality Assurance, you will establish standards for excellence in GCP investigation documentation, root cause analysis, responses, CAPAs, and effectiveness checks to optimize effective and consistent performance within Research and Development, Plasma Derived...