_:ndaaeebb861974594bb705f966ec45b61xb0
<http://schema.org/description>
"&lt;p&gt;&lt;b&gt;Work Schedule&lt;/b&gt;&lt;/p&gt;Standard (Mon-Fri)&lt;p&gt;&lt;/p&gt;&lt;p&gt;&lt;b&gt;Environmental Conditions&lt;/b&gt;&lt;/p&gt;Office&lt;p&gt;&lt;/p&gt;&lt;p&gt;&lt;b&gt;&lt;u&gt;Job Description&lt;/u&gt;&lt;/b&gt;&lt;/p&gt;&lt;p&gt;&lt;/p&gt;&lt;p&gt;&lt;span&gt;As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.&lt;/span&gt;&lt;/p&gt;&lt;p&gt;&lt;/p&gt;&lt;p&gt;&lt;b&gt;&lt;span&gt;A day in the Life:&lt;/span&gt;&lt;/b&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;Provides medical review and analysis for clinical trial serious adverse events, marketed products ICSR and periodic safety reports (e.g. PBRER, PSUR, DSUR), as well as other client deliverables (e.g. labeling reconciliation documents, CTD modules, REMS, RMP, Signal detection reports and CSR).&lt;/li&gt;&lt;li&gt;Maintains understanding of methods for recording time spent on project and administrative tasks, expense submissions and travel.&lt;/li&gt;&lt;li&gt;Ensures tasks delegated to PVG are properly executed. Adheres to applicable regulations and ICH guidelines regarding clinical trials, regulatory documents, and safety issues. Adheres to client SOPs/directives and project specific WPDs for assigned projects. Adheres to PPD’s corporate policies and SOPs/WPDs.&lt;/li&gt;&lt;li&gt;Provides medical consultation to team members and answer all project/study related medical questions. Communicates clearly with associates and clients, maintaining an open line of communication to ensure all procedures are followed appropriately.&lt;/li&gt;&lt;li&gt;Provides safety reporting training on assigned projects/studies, as requested.&lt;/li&gt;&lt;li&gt;Medically reviews adverse event and serious adverse event data from all sources (solicited, spontaneous, literature, etc) as contracted.&lt;/li&gt;&lt;li&gt;Provides medical review of adverse events of special interest, serious adverse events and clinical outcomes events reported in Clinical Trials.&lt;/li&gt;&lt;li&gt;Performs data review as specified in the client contract and data validation manual including review of coding listings and/or full safety data to assess for potential safety concerns.&lt;/li&gt;&lt;li&gt;Assists in writing (interpretation of safety data) and/or review of CSR, IND/NDA report, ICSR, signal detection reports, periodic reports, RMP, REMS, CTD modules, etc. to ensure that the medical content is accurate and complete.&lt;/li&gt;&lt;li&gt;Manages signal detection activities, scientifically reviews periodic safety reports, contributes to label updates, supports dossier maintenance and risk management activities.&lt;/li&gt;&lt;li&gt;Serves as a consultant and spokesperson for the functional area or as an external spokesperson for the organization on highly significant matters. Creates formal networks with key decision makers.&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;/p&gt;&lt;p&gt;K&lt;b&gt;&lt;span&gt;eys to Success:&lt;/span&gt;&lt;/b&gt;&lt;/p&gt;&lt;p&gt;&lt;span&gt;Education/experience:&lt;/span&gt;&lt;/p&gt;&lt;ul&gt;&lt;li&gt;MD or equivalent required. History of an active medical license highly preferred.&lt;/li&gt;&lt;li&gt;Candidates should have at least one of the following:&lt;/li&gt;&lt;li&gt;Clinical experience in having direct responsibility for diagnostic and treatment decisions (comparable to 2 years); Or.&lt;/li&gt;&lt;li&gt;Direct experience in medical review and assessment of safety &lt;span&gt;information/Pharmacovigilance&lt;/span&gt; (comparable to 3 years).&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;/p&gt;&lt;p&gt;&lt;b&gt;&lt;span&gt;Physical Requirements / Work Environment&lt;/span&gt;&lt;/b&gt;&lt;/p&gt;&lt;p&gt;Thermo Fisher Scientific values the health and well-being of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working &lt;span&gt;environment/requirements&lt;/span&gt; for this role:&lt;/p&gt;&lt;ul&gt;&lt;li&gt;Able to communicate, receive, and understand information and ideas with diverse groups of people in a comprehensible and reasonable manner.&lt;/li&gt;&lt;li&gt;Able to work upright and stationary for typical working hours.&lt;/li&gt;&lt;li&gt;Able to work in non-traditional work environments.&lt;/li&gt;&lt;li&gt;Able to use and learn standard office equipment and technology with proficiency.&lt;/li&gt;&lt;li&gt;Able to perform successfully under pressure while prioritizing and balancing multiple projects or activities.&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;/p&gt;&lt;p&gt;Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000&#43; colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.&lt;/p&gt;&lt;p&gt;&lt;/p&gt;"
<https://jobs.thermofisher.com/mx/es/job/TFSCGLOBALR01275485EXTERNALESMX/$%7Beach.locationUrl%7D>