לוח משרות דרושים רוקחות ופארמה

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.

A 100% Tel-Avivian Pharmacy, dedicated to Medical Cannabis, located in the heart of the Florentin quarter - TLV's most vibrant and lively neighborhood.
We're looking for compassionate, knowledgeable certified pharmacists who are interested in taking part in the Israeli Medical cannabis retail industry, from a unique point of view.
We started the Pharmacy in order to disrupt the way medical cannabis is communicated and treated in the country. 
This position will sharpen your existing, and will further equip candidates with valuable skills, useful for their continued development as professionals in the field.
Reach out to us if you feel this is an interesting opportunity.

Our company is a global pharma company on a mission to help patients worldwide get faster access to lifesaving, innovative, breakthrough therapies.
We operate on 4 continents in over 25 countries and are growing fast.
If you want to be part of our mission and help save patients by getting them the latest treatments, join us!
Our company seeks a Therapeutic Area Manager for the Neuro Rare Diseases Unit.
This role includes independently managing a Therapeutic Area.
Outline strategic policies for several fields and products and implement the policy.
Prepare a plan for achieving and maintaining goals.
Managing human resources.
Responsible for the budget of the Therapeutic Area, planning and monitoring it.
Working closely with overseas partners, having an in-depth understanding of the field and KOL's.
Mentoring employees for personal and career development.
Responsibilities:
- Responsible for managing the product managers and human resources within the unit.
- Mentoring team members, product managers, and product specialists.
- Career development for employees.
- Approving and monitoring business plans.
- Involved in building cooperation between marketing units.
- Maintaining strong relationships with overseas partners.
- Business meetings with overseas partners, training sessions, conferences, etc.
- Monitoring and following up on the unit's goals.
- Locate new companies/new products.
- Implement company's principles and vision.
- Report all safety data received within the working framework and pass it on to the PV dept.
- Work by company's code of ethics and guidelines set by the compliance and regulatory dept.
- Report to BUM.