Descrição
Janssen is recruiting for *Medical Science liaison role *to be located in Cairo.
Caring for the world, one person at a time has inspired and united the people of Johnson & Johnson for over 125 years. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world.
Thriving on a diverse company culture, celebrating the uniqueness of *our employees *and committed to inclusion. Proud to be an equal opportunity employer. And our culture is interconnected by the shared values of *Our Credo *. It’s a culture that celebrates *diversity *and diverse perspectives. It helps employees achieve an effective mix between work and home life and supports their efforts to have a positive impact on their communities.
Summary of the job:
The main tasks of *Medical Science Liaison *in *Janssen *are:
To be a therapeutic area scientific expert, responsible for discussing our Therapeutic areas, patients’ treatment trends and studies in the therapeutic areas in which we are involved, on a peer-to-peer basis with a defined audience of Leading Specialists (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other stakeholders) and to be considered a trusted scientific counterpart and partner.
Duties & Responsibilities:
To keep abreast of medical and scientific knowledge.:
Continuously update their knowledge of patient’s treatment trends, guidelines, clinical activities and studies within the therapeutic area and patient's treatment trends in the region
- Identify evolving scientific concepts with future clinical implications.
- Development and maintenance of a *contact network with Leading Specialists *.
- Understand their needs, key value drivers, practical treatment patterns and scientific activities within the therapeutic area.
- *Develop and execute an external stakeholder management plan *in close collaboration and coordination with other functions including HEMAR, Commercial, Global clinical operations, medical information and pharmacovigilance.
- Through scientific interactions, champion the medical value of our products fairly based on the risk-benefit profile of our drugs and contribute to the fostering of innovative approaches.
- Represent the company to other therapeutic area stakeholders including professional associations and patient organisations in cooperation with Medical Advisor(s)/Medical Director
- Recognize and nurture relationships with rising stars within the scientific community.
*Proactive and reactive communication *of medical scientific data to Leading Specialists and broader external health-care related audiences:
Communicate non-promotional general information about our company, including pipeline, research and development programs and other relevant information.
- Respond to unsolicited scientific queries from customers for approved products and products/indications in development, based on Medical Affairs and Medical Information documents.
- Use digital technologies and new media to support proactive and reactive communication.
Organization and participation in Medical Education activities:
Identify/support/educate speakers.
- Build Medical Education programs with scientific third parties and scientific steering committees.
- Participation in *Advisory Boards *in cooperation with Medical Lead/Medical director
Provision of scientific support to company Sales Representatives:
Provide medical and product training and scientific support to Sales Representatives in coordination with Training Departments as appropriate.
- Act as a reference point for sales representatives for any scientific query, in collaboration with Medical Information as appropriate
- Support Medical Affairs *clinical activities' strategy, planning, design and *execution **in close co-operation with GCO and CROs when applicable.
- Support the set up and follow up of registries and other non-interventional Medical Affairs studies.
- Understand *Real World Evidence (RWE) *methodologies, identify data needs and opportunities, support protocol development and engage in discussions with customers to help design RWE projects.
- Propose investigators and sites for interventional and non-interventional Medical Affairs studies.
- Support GCO and CROs in site set up, management and issue resolution.
- Contribute to preparation and conduct of investigator meetings, recruitment follow-up and study result presentation.
- Manage investigator proposals for IISs and ensure they are discussed within the Medical Affairs department for decision.
- Support post marketing surveillance and expanded access programs
- Manage field based medical projects.
- Through scientific interactions, *gain valuable insights *into treatme