Safety Data Associate // Blue Bell PA 19422

Company Description Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at http://www.mindlance.com. Job Description Business                     Safety Data Associate Visa                               GC/Citizen Location                       920 Harvest Drive, Blue Bell PA 19422 Division                        Pharmaceutical Contract                       7 Months Temp-To-Hire Based on performance Timings                        Mon - Fri 8AM – 5PM, extra hours may be required Interview                        Either phone, or Face-To-Face, or Both

Qualifications

Brief Description: · Performs data entry functions and other data functions for the Safety Department

Requirements

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• Degree in a science or health-related field preferred, but not mandatory ·
• Experience in a pharmaceutical company or a service provider (e.g., CRO) highly preferred. ·
• Fluent in English; additional languages a plus, but not required · Proficient with computer programs (Microsoft Outlook, Word, PowerPoint, Excel) · Good communication, interpersonal interaction, and organizational skills are essential ·
• Ability to manage multiple client projects simultaneously with good time management skills Specific Job Duties: · Responsible for Case Receipt, Book-in, accurate Data Entry into safety database in a timely manner ·
• Ensure filing of all documents and organize all filing systems ·
• Assist in the timely and accurate completion of reconciliation activities ·
• Assist in the timely and accurate completion of case processing due diligence activities ·
• Assist in the timely identification of Individual Case Safety Reports and/or relevant safety information during the monitoring of the literature ·
• Support 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 project ·
• Perform self-quality control on entered cases to ensure cases meet highest standards ·
• Participate in project specific internal teleconferences/meeting for operations · Other duties assigned by management Additional Info: · Should have at least 1 year of experience in clinical research, drug safety, or regulatory research (highly preferred) · No Degree Required · Contractors 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 savvy · Should have excellent communication skills, as they will be interacting with Senior staff to ensure case is complete, and some Client staff as well · May be asked to participate in meetings within the department · Position is long term (at least 8 months contract), but they are ultimately looking for long term contractors who they could possibly hire on permanently · Flexible with work schedule, as long as start time is between 8am - 9am, but schedule needs to stay consistent. It can't change from day to day or week to week If you are available and interested then please reply me with your “ Current Chronological Resume” and call me on (678)-405-3590 . Additional Information Thanks & Regards, Ranadheer Murari | Team Recruitment | Mindlance, Inc. | W : 678 405 3590 ranadheerm@mindlance .com