Safety Data Associate // Blue Bell PA 19422

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

Brief Description:

· Performs data entry functions and other data functions for the Safety Department

Requirements:

· 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.

Thanks & Regards,

Ranadheer Murari | Team Recruitment | Mindlance, Inc. | W: 678 405 3590

ranadheerm@mindlance .com