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Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry professionals ensuring the scientific value of our products is realized.
We engage and train internal employees to ensure that they thoroughly comprehend the science behind the medicine and review further unmet medical needs to bolster collaboration and further differentiate our portfolio.
The Medical Science Liaison (MSL) is a credentialed therapeutic and disease expert who engages in scientific exchange with leaders in the external medical and scientific community.
The role provides scientific leaders (SLs) balanced, factual, scientific information about non-product areas of interest to the company and replies to scientific questions from SLs, include questions about Company products. The work of an MSL is aligned to these four core pillars: Scientific Exchange, Research, Scientific Congress Support, and Scientific Insights.
MSLs liaise between the scientific community and the company to enhance the comprehension of scientific foundations and goals for approved, in-development, and active Company-sponsored trials and/or investigator-sponsored research studies.
The MSL serves as a role model for other field medical team members in ways that include on-boarding and/or sharing of therapeutic expertise.
Responsibilities:
Scientific Exchange:
Develops professional relationships and engages with national and/or regional SLs to ensure access to medical and scientific information on areas of therapeutic interest and Company products.
Conducts peer-to-peer scientific discussions and maintains a reliable presence with those SLs to ensure they have a medical contact within the Company.
Addresses scientific questions and directs SL inquiries on issues outside of MSL scope (e.g., grants) to appropriate Company resources consistent with applicable policies.
Maintains current knowledge and comprehension of dynamic scientific and clinical environment in the Company's Areas of Interest (AOI).
Research:
Upon request from Global Clinical Trial Operations (GCTO),
Identifies barriers to patient enrollgment and retention efforts to achieve study milestones, recommends study sites, and identifies potential investigators to participate in phase II-IV clinical development programs.
Addresses questions from investigators and provides information regarding participation in Company-sponsored clinical studies.
Upon request from Scientific Affairs,
Enhances the comprehension of the scientific foundations and goals of investigator-sponsored research.
Identifies barriers to patient enrollment and retention efforts to achieve study milestones.
Initiates discussions with SLs and/or potential investigators that include scientific/data exchange within our AOI to determine the alignment with our research strategies, studies concepts, scientific merit, and qualifications for a specific compound or trial.
Scientific Congress Support:
Engages in scientific and medical meetings through pre-congress preparation.
Facilitates scientific and data exchange for both Company and competitor data and collects meaningful insights.
Staffs congress exhibit booth as applicable.
Scientific Insights:
Gathers feedback, data, or information during routine activities that can help the Company better comprehend medical or scientific needs, priorities, or concerns of healthcare practitioners and/or patients.
Inclusive Mindset and Behavior:
Demonstrates eagerness to contribute to an environment of belonging, inclusion, equity, and empowerment.
Leads by example and serves as a role model for creating, leading and retaining a diverse and inclusive workforce.

We are looking for a Regulatory & Safety Manager.
This pivotal Regulatory Manager role offers you the opportunity to champion collaboration across teams, enhancing your leadership abilities. As the bridge between Reckitt and regulatory agencies, your expertise will be key in guiding our innovative products through complex regulatory landscapes to reach consumers safely and efficiently.
Your responsibilities:
Manage and coordinate all aspects of regulatory affairs on full portfolio
Responsible for local regulatory team including Development plan, Growth and proper knowledge and expertise
Ensure all registration objectives financial targets are met
Ensure full compliance with local & global requirements towards regulatory activities
Effectively manage Pharmacovigilance
Have responsibility for defining and adapting regulatory strategies and implement them across defined categories
Complying with Global standards and local procedures and help providing safe, effective and compliant products to customers, consumers and patients.