Medical Information & Pharmacovigilance alliance Graduate
We offer an exciting 2-year graduate programme for graduates that are looking to work with us to deliver on our mission to save and improve lives. Our programme will give you the opportunity to collaborate alongside subject matter experts, bring your own ideas and share real responsibility whilst delivering on meaningful projects alongside a passionate, diverse and inclusive workforce.
Who we are…?
We are a global biopharmaceutical leader with a diverse portfolio of prescription medicines, oncology, vaccines and animal health products. We are driven by our purpose to develop and deliver innovative products that save and improve lives. With over 70,000 employees operating in more than 140 countries, we offer state of the art laboratories, plants and offices that are designed to Inspire our employees as we learn, develop and grow in our careers. We are proud of over 125 years of service to humanity and continue to be one of the world’s biggest investors in Research & Development.
We are officially certified by the Top Employer Institute and been awarded the exclusive Top Employer United Kingdom Certification for the third year running.
Our Medical Affairs team advances patient care by engaging in scientific exchange with external medical experts and industry leaders ensuring the scientific value of our products is understood. We connect, communicate and train internal employees to ensure a thorough understanding of the science behind the medicine and review further unmet medical needs to support collaboration to further differentiate our portfolio.
Our 24 Month Graduate scheme encompassing two 12-month rotations in Medical Information (London/Remote) and Pharmacovigilance (London/Remote)
Where do you start…?
12 months in Medical Information – based in London/Remote
You will begin your journey within Medical Information, within the Medical Affairs team, where you will be responsible for providing high-quality, non-promotional and unbiased medical and scientific information across a range of therapeutic areas and preparing scientific content for internal and external customers.
Duties & responsibilities
12 months in Pharmacovigilance – based in London
Within Pharmacovigilance (PV) you will be responsible for day-to-day adverse events case management including case intake and follow-up activities in accordance with Global Safety procedures, the review of local literature as per company procedures and country regulations, and health authority submissions of cases in accordance with Global Safety procedures and health authority standards.
Duties & responsibilities
Qualities we look for
What happens at the end of the 24-month scheme?
Throughout the 24 month scheme you will receive guidance and mentoring to not only help you through your current role, but also to prepare you for applications to permanent roles within the organisation, with the aim that you will continue your career journey with us.
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