UnitedHealth Group is among the most ambitious Fortune 25 companies
you'll ever meet. Through our family of businesses, we're working to
make the health care system perform better for more people, in more
ways than ever.
Simply put, we think the entire system can be greater than it's ever been. And that drives us to work harder, aim higher, and expect more from one another.
Here,
you'll be empowered to make an immediate impact for millions of others.
And you'll achieve more than you ever expected. How does that fit with
your plans?
Job Description
i3 Pharma Resourcing provides high-quality pharmaceutical personnel supported by world-class service. We draw on our clinical understanding and global resources to match the best individual for the unique needs of the job, then provide ongoing support and personal development.
We have both contract and permanent positions available. We offer competitive rates and a benefits package that is second to none in the industry!
Job Requirements
M onitors the safety profile of the registered/marketed products in collaboration with Global Pharmacovigilance and Epidemiology (GPE). Oversees the local clinical assessment and approval for all individual adverse reactions, product technical complaints and/or serious individual adverse events either unsolicited or collected from appropriate solicited sources (Phase IV clinical studies, compassionate use, intensive monitoring) leading to adverse event reports. Facilitates safety data analysis and management by optimizing the quality documentation and assessment of individual reports from clinical studies and all post marketing events involving sanofi-aventis products. Oversees data management into the Pharmacovigilance database. Ensures compliance with sanofi-aventis SOPs related to the collection, evaluation, analysis and reporting of adverse experience reports. Detects and evaluates potential safety signals in collaboration with the US-RiSC group and GPE.
Experience:
3 - 5 years Public Health or general practice experience.
Minimum 3 years experience in Safety Surveillance, Pharmacovigilance or Drug Safety managing spontaneously reported adverse events.
3+ years of total experience in the pharmaceutical industry, partly in related areas, such as Medical Affairs, Clinical trials management, Regulatory Affairs or Quality Assurance is a plus.
Education:
MD or equivalent degree with postgraduate specialization in either a primary care or a subspecialty.
Has a valid license to practice medicine within the United States or a foreign medical degree with clinical practice experience.
Clinical practice experience preferred.
Diversity creates a healthier atmosphere: equal opportunity employer M/F/D/V.
UnitedHealth Group is a drug-free workplace. Candidates are required to pass a drug test before beginning employment.