Global Coordinator, Pharmacovigilance

Organization
GE Healthcare
Job Location
Marlborough, MA
Job Description

GE is the world's Digital Industrial Company, transforming industry with software-defined machines and solutions that are connected, responsive and predictive. Through our people, leadership development, services, technology and scale, GE delivers better outcomes for global customers by speaking the language of industry. 
There is no other life sciences company quite like GE Healthcare Life Sciences. A $5 billion business with 
more than 11,000 individuals in over 100 countries, we are at work enabling a new era in medicine. For 
more than 60 years, GE Healthcare Life Sciences has globally supported the development and use of new therapies, helping accelerate the journey from biological understanding to clinical therapy. GE Healthcare Life Sciences works with cutting edge technology enabling and advancing the discovery, diagnosis and medical treatments of the present and the future. We are accelerating biology to cell therapy in ways no other company can. 
Follow us on Facebook and Twitter and watch our discoveries in action on our YouTube channel. 
Learn More About GE Healthcare - Life Sciences 
Learn More About Careers at GE Healthcare - 
Life Sciences 
GE offers a great work environment, professional development, challenging careers, and competitive compensation. GE is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.The Global Coordinator interacts proactively with Local Safety Units (LSUs) and distributors to ensure that all adverse event reports received locally are reported to the GEHC Pharmacovigilance (PV) Central Safety Unit (CSU) in a timely manner as specified in PV SOPs. This individual is also responsible for distributing adverse event reports to LSUs and distributors and for monitoring and managing the electronic export and import of adverse event reports from global regulatory authorities. 

Role Summary/Purpose 
The Global Coordinator interacts proactively with Local Safety Units (LSUs) and distributors to ensure that all adverse event reports received locally are reported to the GEHC Pharmacovigilance (PV) Central Safety Unit (CSU) in a timely manner as specified in PV SOPs. This individual is also responsible for distributing adverse event reports to LSUs and distributors and for monitoring and managing the electronic export and import of adverse event reports from global regulatory authorities. 

Essential Responsibilities 
•Interact proactively with LSUs and distributors to ensure that all adverse event reports received locally are reported to the GEHC CSU unit in a timely manner as specified in PV SOPs 
•Monitor workflow status of adverse event reports in the global adverse event database to ensure compliance with case processing timelines 
•Perform daily review in global adverse event database to ensure distribution of adverse event reports to LSUs, distributors and partners 
•Monitor acknowledgment receipts/responses from electronic submissions of adverse event reports to global regulatory authorities, LSUs, Partners and Distributors and address transmission errors 
•Monitor electronic imports into global adverse event database and submit to workflow for processing 
•Assist with other case processing activities as needed 
•Performs other duties and responsibilities as assigned 

Quality Specific Goals: 
•Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position. 
•Complete all planned Quality & Compliance training within the defined deadlines. 
•Identify and report any quality or compliance concerns and take immediate corrective action as required

Requirements: 
Qualifications/Requirements 
•Bachelor of Science degree (Life Sciences Background) 
•Minimum of 2 years of pharmaceutical/biotechnology industry with experience in 
Pharmacovigilance/regulatory affairs including clinical trials and postmarketing. Global experience highly preferred. 
•In-depth knowledge of Individual Case Safety Report (ICSR) processing with hands-on 
experience coordinating and monitoring ICSR workflows and reporting ICSRs to global regulatory agencies 
•Proficient in performing data entry, retrieval and electronic reporting in global drug safety databases 
•Familiar with US/EU/AP/LA regulations and ICH guidelines pertaining to adverse event reporting 
•Proficient in use of Microsoft Office (Word, Excel, PowerPoint, Outlook) 

Desired Characteristics 
•High integrity, sense of urgency and ability to recognize time sensitivity 
•Excellent organizational, interpersonal skills, problem solving and negotiation skills 
•Excellent written and verbal communication skills 
•Being open to change (positive or negative) in response to new information, different or unexpected circumstances, and/or to work in ambiguous situations 

Additional Eligibility Qualifications 
GE will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a background investigation and drug screen. 

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