Local Medical Safety Specialist

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
Product Safety

Job Sub Function:
Pharmacovigilance

Job Category:
Scientific/Technology

All Job Posting Locations:
Istanbul, Turkey

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for a Medical Safety Specialist.

This position will be located in Istanbul, Turkey.

Essential Job Duties and Responsibilities

The position is responsible for supporting the compliance of LOC Safety activities of TURGAN cluster by mainly focused on Turkiye, covering medicinal products, with local regulations, company policies, and global standards, including any Product vigilance agreements with third-party partners.

 It involves assisting in establishing and maintaining effective Pharmacovigilance and Risk management systems and supporting the oversight of the products within its responsibility.

The role includes contributing to the proactive management of Benefit Risk Management throughout the product life cycle, tailoring actions to local needs.

Additionally, it involves aiding in safety reporting requirements as needed by Marketing Authorization Holders (MAH) and study sponsors, as applicable.

Safety Management & Reporting

Oversight and Providing Input


* Support Data-generating Activities: Assist in overseeing data-generating activities to ensure appropriate review and reporting processes are included in project documents for reporting potential Adverse Events (AEs), such as patient support programs, market research surveys, and internet sites, as applicable.

Provide support to the Hub for Related Research Activities (RRA) activities, where applicable.


* Vendor Contracts: Ensure, in collaboration with the Hub if applicable, that all vendor contracts have appropriate Pharmacovigilance language incorporated and that these contracts are archived in the global system, as applicable.


* Product Portfolio Oversight: Support the oversight of the full product portfolio and establish links with local management and key stakeholders.

Assist in overseeing the safety ...