Clinical Development Medical Director - Cardiology job opportunity at Novartis.

Home Jobs In United Kingdom Tag: Job Clinical Development Medical Director - Cardiology position at Novartis


DateMore Than 30 Days Ago bot
Novartis Clinical Development Medical Director - Cardiology
Experience: 4-years
Pattern: full-time
Country:
apply Apply Now
Salary:
Status:

Job

Copy Link Report
degreeAssociate
loacation London (The Westworks), United Kingdom
loacation London (The We..........United Kingdom

Job Description Summary As a Clinical Development Medical Director, you will be responsible for the scientific and clinical strategy of assigned clinical trials, scientific monitoring, and reporting of quality data. The Clinical Development Medical Director (CDMD) is the clinical leader of defined program level activities (e.g., submission activities, briefing books, clinical study reports, etc.) and/or a large, complex trial, under the leadership of the Global Program Clinical Head (GPCH). May also lead a section of a clinical program (e.g., an indication, a new formulation, or a specific development phase).   Job Description #LI-Hybrid Location: London UK, Barcelona Spain or Dublin, Ireland Major accountabilities: Provide clinical leadership and medical strategic input for deliverables in the assigned project/program. Deliverables may include sections of individual protocols consistent with the clinical development plan (CDP), data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications (e.g., investigator brochures, briefing books, safety updates, submission dossiers, and responses to health authorities) Drive execution of the section of the program in partnership with global line functions, assigned Global Trial Directors, and regional/country medical associates Oversee/conduct medical and scientific review of trial data with Clinical Scientific Expert (CSE). May be the Program Manager of other associates (e.g.., CSE). May function as study medical monitor Support GPCH in ensuring overall safety of the molecule. May be a core member of the Safety Management Team, and supports program safety reporting (e.g., PSURs, DSURs, and safety related documents) in collaboration with Patient Safety Support the Clinical Development Head by providing medical input into CDP and clinical trial package reviews and contributing/driving development of disease clinical standards for disease areas Provide support to the GPCH or CDH in interactions with external partners (e.g., regulatory authorities, key opinion leaders, data monitoring boards, advisory boards, patient advocacy groups), internal partners (e.g., clinical trial team, Medical Affairs, Commercial, Health Economics & Outcomes Research), and decision boards) Work with BR (Novartis Biomedical Research)/Translational Medicine) to drive transition of early development projects to Transition Decision Point and with Business Development, including target identification and due diligences Ensure career development of Program Reports and clinical colleagues through active participation in performance management and talent planning processes. Provide on-boarding, training, & mentoring support Contribute to medical/scientific training of relevant Novartis stakeholders on the disease area and compound/molecule. May serve as speaker for Global Clinical team Minimum Requirements: MD (or equivalent medical degree) required. Training in cardiology preferred Medical Board certification preferred. 4+ years Clinical practice experience (including residency) preferred Possess advanced knowledge and clinical training in a medical/scientific area (e.g., internal medicine or sub-specialty) required 5+ years of experience in clinical research or drug development from the pharmaceutical/biotechnology industry, preferably spanning clinical activities in phases I through IV 3+ years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting, and publishing) in a global/matrixed environment Showcase advanced knowledge of assigned therapeutic area Demonstrate ability to establish strong scientific partnership with key partners Need thorough knowledge of Good Clinical Practice, clinical trial design, statistical analysis methodology, and regulatory/clinical development processes People management experience preferred, especially at the global level (this may include management in a matrixed environment) Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.  Read our handbook to learn about all the ways we’ll help you thrive personally and professionally:  Novartis Life Handbook   Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.    Skills Desired Clinical Trials, Cross-Functional Teams, Data Analysis, Data Monitoring, Drug Development, Drug Discovery, Medical Research, Medical Strategy, People Management

Other Ai Matches

Senior Product Specialist Applicants are expected to have a solid experience in handling Job related tasks
Vodja tehnoloških prenosov (m/ž/d) / Technical Transfer Lead (m/f/d) Applicants are expected to have a solid experience in handling Job related tasks
Tehnik v proizvodnji bioloških učinkovin (m/ž/d) Applicants are expected to have a solid experience in handling Job related tasks
Global Regulatory Affairs Associate Director (Cardio-Metabolic) Applicants are expected to have a solid experience in handling Job related tasks
Clinical Data Engineering Lead Applicants are expected to have a solid experience in handling Job related tasks
Sr. Specialist- Solution Delivery for Infrastructure Services- AWS/ Azure Applicants are expected to have a solid experience in handling Job related tasks
Senior Business Analyst, Data Digitial & IT Applicants are expected to have a solid experience in handling Data Digitial & IT related tasks
Manager, Content Strategy Applicants are expected to have a solid experience in handling Content Strategy related tasks
Senior Expert - QC Applicants are expected to have a solid experience in handling Job related tasks
Direktor terapevtskih področij (m/ž/d) / Therapeutic Area Head (m/f/d) Applicants are expected to have a solid experience in handling Job related tasks
Legal Intern Applicants are expected to have a solid experience in handling Job related tasks
Senior Principal Clinical Data Scientist Applicants are expected to have a solid experience in handling Job related tasks
Key Account Manager Applicants are expected to have a solid experience in handling Job related tasks
Campaign Delivery Manager Applicants are expected to have a solid experience in handling Job related tasks
Tehnolog proizvodnih procesov (m/ž/d) / Process Expert (m/f/d) Applicants are expected to have a solid experience in handling Job related tasks
Director, Principal Consultant Applicants are expected to have a solid experience in handling Principal Consultant related tasks
Chef de produit Junior en stage Applicants are expected to have a solid experience in handling Job related tasks
Senior Metrologist Applicants are expected to have a solid experience in handling Job related tasks
Director - Integrated Field Insights & Analytics Applicants are expected to have a solid experience in handling Job related tasks
Senior Analyst, Competitive Intelligence Applicants are expected to have a solid experience in handling Competitive Intelligence related tasks
Tehnik v proizvodnji farmacevtskih učinkovin (m/ž/d) Applicants are expected to have a solid experience in handling Job related tasks
Facility Manager Applicants are expected to have a solid experience in handling Job related tasks
Manufacturing Specialist (weekend night shift) Applicants are expected to have a solid experience in handling Job related tasks