At AstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the utmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people's exceptional skills with those of people from all over the globe. As a Senior Pharmacovigilance Medical Director
in Gaithersburg, MD
, you'll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives. GMD
(Global Medicines Development) drives late-stage development of our innovative pipeline, transforming exciting science into valued new medicines and ensuring patients around the world can access them.
AstraZeneca holds a unique position in Respiratory Disease
, including asthma, chronic obstructive pulmonary disease (COPD) and idiopathic pulmonary fibrosis (IPF), with a range of differentiated potential medicines in development by leveraging novel combinations, biologics and devices. The pipeline also has a number of promising assets in inflammatory and autoimmune diseases within areas such as psoriasis, psoriatic arthritis, gout, systemic lupus and rheumatoid arthritisMain Duties and Responsibilities
As the Senior Pharmacovigilance Medical Director you will be responsible for recruiting and managing a team of safety physicians which contributes to ensuring that an adequate number of qualified physicians and staff is available for Patient Safety to satisfy AstraZeneca's objectives in the Patient Safety area. You will be expected to act as delegate for the TA VP of Patient Safety. You will ensure that your own work and work of team is compliant with relevant internal and external regulations and standards. You will use your expertise and knowledge of global issues to develop strategic Physicians and Scientists objectives for inclusion into business objectives. You will be responsible for providing Disease Area strategic input to a group of drugs in development and post-marketing programs across life-cycle of these substances and products. You will be defining strategies or lead AstraZeneca's response to complex technical issues for specific safety aspects in relation to current drug projects, new drug projects and various improvement plans. You will represent content matter expertise at high level decision-making bodies. You must be able to work across a number of disease areas in the TA and oversee delivery. You must be able to represent Patient Safety in external regulatory meetings. You will influence our strategy and the Patient Safety interface with all Clinical Development groups and Regulatory Affairs leads in the TA and with the Commercial organization. You will review regulatory communication and preparation of higher level documents. You will closely follow medical developments within assigned areas and disseminates new information within Patient Safety to transform trends and emerging data into new plans. You will follow important developments and trends in scientific literature and develops contacts with opinion leaders.Essential Requirements
- Degree in medicine and experience as a physician or academic
- Experience in providing strategic leadership to complex drug projects
- Relevant industry experience in Pharmacovigilance field
- Experience in managing a scientific team
- Demonstrated ability to influence key stakeholders within and outside of company
- Demonstrated proficiency with both written and verbal communications
Next Steps - Apply today!
- PhD in scientific discipline
- Extensive general medical knowledge
- Able to work across TAs and Functions
- Research background including peer reviewed publications
To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience - it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity. If you know someone who would be a great fit, please share this posting with them.
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.