Description:

24 months Programme based in the Scientific Enablement & Pharmacovigilance team

* Who we are *

The Team

Throughout the development of our drugs it is essential to making sure our products are safe to use in humans, and that side-effects are well understood and managed.

Our team manages communication and education of safety risks with medicines. We are therefore looking for a great communicator who can capture case studies from our clinical teams and create engaging and interesting content to highlight their work.

You would be joining a team of Global Process Experts in the Pharmacovigilance & Scientific Enablement team within the Medicines Safety Organization at Roche. The specific Risk Management (RM) project team is a small team led by the RM Global Process Owner.

Key Responsibilities

* Contribute to a project team to improve patient and healthcare professional communications which focus on identifying and managing side-effects (known as risk management tools)

* The project aims to support clinical safety teams to :

* consider testing tools in clinical trials

* to identify and highlight innovative new tools

* selecting the best tools available for product launch and

* to measure the effectiveness of the tools

* Embed regular review of data throughout the medicine lifecycle

* The role would be supporting this project with specific deliverables: For example capturing team experiences and producing online content in engaging ways

* Creating engaging best practice content for Clinical Safety Teams

* Reviewing tools used across molecule teams and connecting people

* Engaging with teams and people in UK, Switzerland and USA

*Who you are*

Soft Skills

* Uses initiative to make suggestions for improvements

* Bring ideas on new ways to do things

* Verbal and online communication skills

* Team player: works with team members of project and clinical teams and wider Roche teams

* Confidence in contributing to meetings and leading assigned work (with support)

* Ability to build relationships and networks with people virtually

* Digital literacy

* Connect the Dots between ideas, data, teams

* Enthusiastic to learn more about medicines safety, regulatory science and specifically risk management

Skills

* To work with Clinical Safety teams to capture stories on best practice, lessons learned and innovation

* To develop online information in interesting and engaging ways

* To review and compare tracking and compliance data

* Review of global tracking data to ensure targets have been met and identify when not met

* Ability to produce google/ excel sheets to track

* Ability to produce slides to support meetings/ presenters

* Ability to use databases and common IT packages e.g. Microsoft and Google suite

* Understands project teams goals and contributes to delivery of them

* To communicate with local country offices to explore and document reasons where targets have not been met

* To work with Roches' Clinical Safety community to support their Risk Management tool selection and effectiveness

* Organize meetings and note actions where needed

*Application Process*

Phase I:

Purpose - our focus on this first stage is to understand why you have applied for this role and what you will bring to the role to ensure team and personal success.

* * Cover letter & CV *

* * Video interview *

As part of your cover letter, Roche is keen to understand your motivation in applying for this position. You should, therefore, provide responses to the following:

* *Why Roche: What do you know about Roche and why do you want to work here?*

* *Why you: If you had to choose a single example or achievement in your life, that you feel would make you suitable for this role, what would it be and why?*

Your cover letter should not exceed one page.

** note any application without a cover letter will be automatically rejected. **

Phase II:

* Final Assessment Centre

Check out application tips and tricks HERE :

Job Details