Résumé
About the Role
Location
This role is either based in Dublin (Hybrid office/home) OR UK (Homebased)
Your responsibilities include, but are not limited to:
- Prepares / supports the preparation of highly complex scientific documents to meet highest quality standards.
- Initiates, implements and champions process improvement techniques. Manages multiple projects across multiple brands and therapeutic areas. Defines and implements customer management strategies and tactics. Develops a Center of Excellence (CoE) for identified TA/disease area/deliverable.
- Provides strategic inputs to development and brand plans and assists in policy decision making as TA/disease/deliverable champion.
- Ideates and implements tactics to influence internal and external development environment.
- Complies with and support group’s project management tool, standards, policies and initiatives.
- Follows Novartis specifications for documentation, templates etc. Maintains records for all assigned projects including archiving. Maintains audit, SOP and training compliance. Trains new joiners, fellow colleagues as and when required. Performs additional tasks as assigned.
Key Performance Indicators
- Preparation of the above referenced documents meeting set quality standards and on time for submission to Health Authorities/ Clinical teams / Journals as appropriate. (i.e. complying with standards e.g. CONSORT regarding publication of trial results, complying with journal formatting requirements etc).
- Derive maximum efficiency from the teams working on projects assigned. Publications are acceptable to internal and external authors (no issues with authorship).
- Completion of an adequate number of medical and scientific documents (taking into account complexity) per year.
- Active contribution to knowledge creation, use and dissemination activities. Adheres to Novartis values and behaviors.
Requirements
Education (desirable):
- Minimum: Minimum science degree or equivalent, B.Sc./equivalent with 12 years Clinical Research (CR) experience, M.Sc./M.Pharm +10 years of clinical research (CR) experience
- Desired: Doctoral Degree or Qualification in Medical Sciences
(MBBS/MD/equivalent)
PhD > 8 year of CR experience, MBBS/equivalent >8 year of
CR experience, MD >6 years of CR exp
- Excellent written and oral English
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
