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Drug Safety Associate

  2026-08-03     Mindlance     Blue Bell,PA  
Description:

Safety Data Associate // Blue Bell PA 19422ContractMindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at Safety Data AssociateLocation 920 Harvest Drive, Blue Bell PA 19422Division PharmaceuticalContract 7 Months Temp-To-Hire Based on performanceTimings Mon - Fri 8AM – 5PM, extra hours may be requiredInterview Either phone, or Face-To-Face, or BothBrief DescriptionPerforms data entry functions and other data functions for the Safety DepartmentRequirementsDegree in a science or health‑related field preferred, but not mandatoryExperience in a pharmaceutical company or a service provider (e.g., CRO) highly preferred.Fluent in English; additional languages a plus, but not requiredProficient with computer programs (Microsoft Outlook, Word, PowerPoint, Excel)Good communication, interpersonal interaction, and organizational skills are essentialAbility to manage multiple client projects simultaneously with good time‑management skillsSpecific Job DutiesResponsible for Case Receipt, Book‑in, accurate Data Entry into safety database in a timely mannerEnsure filing of all documents and organize all filing systemsAssist in the timely and accurate completion of reconciliation activitiesAssist in the timely and accurate completion of case processing due diligence activitiesAssist in the timely identification of Individual Case Safety Reports and/or relevant safety information during the monitoring of the literatureSupport and interact with Team Managers Global Case Processing/(Sr) Safety Scientists Global Case Processing to discuss ongoing projects.Be aware of and maintain the workflow and timelines for each projectPerform self‑quality control on entered cases to ensure cases meet highest standardsParticipate in project specific internal teleconferences/meetings for operationsOther duties assigned by managementAdditional InfoShould have at least 1 year of experience in clinical research, drug safety, or regulatory research (highly preferred)No Degree RequiredContractors will be performing data entry from forms into a database (will be trained on the database being used, but previous experience would be a plus)Should be tech savvyShould have excellent communication skills, as they will be interacting with Senior staff to ensure the case is complete, and some Client staff as wellMay be asked to participate in meetings within the departmentPosition is long‑term (at least 8 months contract), but they are ultimately looking for long‑term contractors who they could possibly hire on permanentlyFlexible with work schedule, as long as the start time is between 8am – 9am, but the schedule needs to stay consistent. It can't change from day to day or week to weekIf you are available and interested then please reply with your “ Current Chronological Resume ” and call me on (678)-405-3590 .Thanks & Regards#J-18808-Ljbffr


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