לוח משרות דרושים רוקחות ופארמה

Are you looking for a new way to apply your clinical knowledge to help improve patient care and
the lives of others? Are you interested in being at the forefront of healthcare technology and
thrive in a fast-paced environment? MDI Health is looking for a passionate and innovative
pharmacist with a strong clinical background to join our team. This position would be working
primarily with our Operations and Clinical Research and Development teams, and involves a
variety of responsibilities (listed below) with the opportunity for growth as the position and
organization evolves.

What youll do:

Work in the Clinical R&D team on enhancing existing features and developing new ones
Compose and present insights gathered from clients feedback
Clinical QA including reviewing therapy recommendations and data for clinical
accuracy and completeness
Update the system based on scientific literature and professional guidelines
Additional responsibilities:

Provide clinical support to MDI clients and vendors as needed by answering clinical
questions, providing product training to pharmacist users during the onboarding &
implementation process and assisting our client support team
Provide clinical support to the Sales, Implementation, and Account Management
teams by contributing to product configuration decisions and lending clinical expertise

We are looking for a Medical writer and Regulatory Affairs associate.
Primary function of the position:
Clinical scientific knowledge and writing skills to effectively and clearly communicate medical science information in writing. Generally, focus on either scientific medical writing, which includes clinical studies, and regulatory documents, scientific articles or marketing medical writing. Experience in regulatory aspects (RA), help to lead regulatory strategy and provide ongoing regulatory input.
Roles and Responsibilities:
Work with clinical teams and clients to understand the nature of the scientific work that they will be covering.
Assess data or products using medical expertise, and quickly develop expertise in new areas as needed for their writing.
Help to write studies for submissions to the FDA. The writing is also used in publications or medical journals, or for internal company use.
Comprehensive writing of clinical study reports, study protocols, annual reports, investigator brochures, risk/benefit analysis and integrated summaries from raw data.
Prepare abstracts, scientific exhibits, posters and verbal presentations.
Help with develop and write pharmaceutical training materials, eLearning content, video scripts, magazine articles, and presentations to be used by a variety of audiences.
Conduct comprehensive literature searches to enhance background understanding, and evaluate and analyze the information which will be written about.
Provide responses to regulatory agencies regarding product information or issues.
Maintain current knowledge of relevant regulations, including proposed and final rules. Help in manage activities such as audits, regulatory agency inspections etc.
Participate in the development or implementation of clinical trial protocols. Preparation and submission of regulatory agency applications, reports, or correspondence.
Provide regulatory guidance to departments or development project teams regarding design, development, evaluation, or marketing of products.