Medical Scientific Liaison Immunology

5 days ago

مصر, Egypt Johnson & Johnson Full time

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

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