Clinical Trial/CRO Medical Monitor - Safety Data Analyst I

The Medical Monitor/ Safety Data Analyst processes Adverse Event (AE) and Serious Adverse Event (SAE) cases promptly and with medical accuracy. The Medical Monitor/ Safety Data Analyst will also assist the Head of Safety and Pharmacovigilance Department with Medical Coding and Medical Monitoring activities and oversees the overall conduct of pre- and post-marketing studies regarding safety of the subjects for his/her studies, and as a back-up for other Medical Monitors.

• Oversee the overall conduct of pre- and post-marketing studies regarding Safety of study subjects for the assigned studies.
• Perform medical review of Protocols, Investigator’s Brochures, Case Report Forms, Informed Consent forms, and Clinical Study Reports according to the Scope of Work
• Have a good understanding of all projects related to Safety and Coding.
• Interacts with Sponsors/Clients directly with minimal or no supervision for the assigned studies and other projects, as needed.
• Direct assigned Safety designees of each assigned projects with regard to Safety and Coding activities. 
• Develop Pharmacovigilance, Safety Management and Medical Monitoring Plans
• Lead coding procedures of medical data including medications (utilizing WHODrug), adverse events and serious adverse events (utilizing MedDRA)
• Prepare safety case reports to the FDA and regional regulatory agencies using MedWatch and CIOMS-I forms, and annual/ periodic safety reports. 
• Oversee Processing, Documentation, and Reporting of Adverse Event and Serious Adverse Event Information to the Client, and the FDA
• Prepare safety narratives 
• Maintain, review, and reconcile safety and clinical databases for paper-based studies
• Evaluate safety trends, and pharmacovigilance risk assessment in collaboration with the biometrics department according to the Scope of Work. 
• Assure that the required study documents are complete, accurate, and in accordance with required global and region-specific regulations and guidelines 
• Participate in sponsor audits as required
• Participate in Bid Defense meetings.
• Provide support for the audits of clinical sites according to the Scope of Work.
• Participate in project team meetings as required
• Participate in Data Safety Monitoring Committees (DSMC), provide and present safety and pharmacovigilance reports for the DSMC meetings for various sponsors, as applicable
• Communicate orally and /or in writing, in a timely and effective manner, with the appropriate internal or external individuals involved in the project, including serving as the Medical Point of Contact for Investigator, and Sponsor teams. 
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• Medical Degree required (e.g., M.D./D.O.)
• Knowledge of global and region-specific regulations and guidelines including ICH, US and EU, UK regulations. 
• Knowledge of Adverse Event processing environments such as ArisGlobal or similar is preferred.
• Exceptional and effective verbal and written communication skills to facilitate and complete concise safety reporting.
• Experience with Safety audits of clinical trials is preferred
• Experience with Electronic Data Capture system (EDC)
• Ability to work in a fast-paced environment, handling multiple projects with high degree of accuracy and attention to detail.
• Basic understanding of clinical bio-statistical analysis, and the ability to think critically, analyze data, and problem solve. 
• Ability to work independently as well as in a team environment contributing to a collaborative work atmosphere.
• Experience in communicating with Regulatory Agencies, Data Safety Monitoring Committees (DSMC), Sponsors, and Principal Investigators is preferred. 
• Experience working with MedDRA and WHODrug dictionaries is preferred. 
• Proficient in the use of Microsoft Office Software. 

Salary Range: $102,00 - $133,000 USD

The total pay range takes into account a wide range of factors that are considered in making compensation decisions including, but not limited to, skills; experience and training; licensure and certifications; and other business and organizational needs. The disclosed pay range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. At NSF, it is not typical for an individual to be hired at or near the top of the pay range for their role and compensation decisions are dependent on the facts and circumstances of each case.

With a legacy spanning more than 80 years, NSF leverages science and innovation to improve human and planet health. We provide science-driven, independent testing, inspection, certification, and advisory services and develop the very standards that drive the food, water, and life sciences industri