Singapore Global Safety Vigilance Risk Management Lead
Singapore Global Safety Vigilance Risk Management Lead
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
1. Considering impact on subject/patient safety and product value maximization from development to postmarketing stage.
2. Flexible mindset and refined negotiation skill to achieve challengeable targets.
3. Act as Product Safety Lead with responsibility for risk management activities as below for Santen investigational and postmarketing products.
- Preparation of signal assessment documents
- Creation of action plans to mitigate/manage product risks
- Development and maintenance of product Core Risk Management Plans (cRMP) and Company Core Safety Information (CCSI)
- Preparation of aggregate safety report such as PSUR
- Development of clinical trial relevant documents such as DSUR safety management plan periodic risk monitoring of investigational products
- Preparation for safety relevant documents at NDA/MAA dossier in cooperation with other SV members and relevant stakeholders
- Contribute to R&D project as a representative of SV with scientific and strategic input.
4. In addition provides support to SV related activities/projects globally according to the direction made by head of PharmacoEpidemiology at any given time.
Qualifications :
- Experience in drug safety activities but not limited in PV function in pharmaceutical companies (e.g. pharmacovigilance medical affairs medical science liaison regulatory affairs R&D clinical development nonclinical research etc.) for more than 5 years.
- Bachelors degree in Life Science or a related field preferably pharmacist.
- High compatibility with scientific and strategic way of thinking to find solution even in complicated situations.
- Experience in cross functional and regional projects (e.g. R&D project).
- Experience in risk management for medicinal product .
- Knowledge of products development process including preparation for NDA/MAA dossier.
- Familiarity with and ability to work as a standalone or a few members of Pharmacovigilance unit within a global Safety Vigilance Structure
- Wellorganized and detail oriented with strong verbal and written communication skills in English
- Ability to effectively participate in multidisciplinary teams; strong handson leadership
- Solid decisionmaking skills interdependent partnering skills teamorientation and demonstrated ability to influence outcomes.
- Solid computer skills using MS Office / Word.
Additional Information :
Grow your career at Santen
A career at Santen is an opportunity to make a difference. Through our longterm vision outlined in Santen 2030 we are committed to be a Social Innovator addressing the social and economic needs of people with visual impairments. We have team members around the world using their diverse talents to unlock new modalities and drive innovations for patient outcomes education and treatment. At Santen we believe in empowering all our team members with flexible ways of working and a highly inclusive work environment.
The Santen Group is an Equal Opportunity Employer. We are committed to building diverse teams and ensuring a safe and inclusive physical and virtual workplace for every one of our team members. All employment decisions are based on business needs role requirements and individual qualifications regardless of race color ethnicity national origin/ancestry religion sexual orientation gender gender identity/ expression age disability medical condition marital status veteran status or any other characteristic protected by law.
If you require any kind of accommodation during our recruitment process please let the recruiter from our team know.
Remote Work :
No
Employment Type :
Fulltime
Employment Type
Full-time
