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Drug Safety Analyst

Belcan

Los Angeles, CA

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JOB DETAILS
SALARY
$42–$45.70 Per Hour
SKILLS
Administrative Skills, Analysis Skills, Business Administration, Business Support, Change Management, Communication Skills, Computer Systems, Data Administration, Data Analysis, Data Collection, Data Management, Database Administration, Detail Oriented, Documentation, Establish Priorities, File Systems, GMP (Good Manufacturing Practices), Green Business, Health Science, Information Systems/Technology IS/IT Administration, Information Technology & Information Systems, Interpersonal Skills, Medical Coding, Medical Dictionary for Regulatory Activities (MedDRA), Medical Terminology, Microsoft Excel, Microsoft Office, Microsoft PowerPoint, Microsoft Visio, Microsoft Windows 7, Microsoft Word, Multitasking, Operational Support, Organizational Skills, Performance Reviews, Pharmacovigilance, Presentation/Verbal Skills, Problem Solving Skills, Procedure Development, Process Flow Diagram (PFD), Product Marketing, Project Execution, Regulations, Regulatory Compliance, Regulatory Reports, Regulatory Requirements, Regulatory Submissions, SAP BusinessObjects, Safety Process, Software Administration, Standard Operating Procedures (SOP), System Validation, Systems Administration/Management, Technical Delivery, Technical Writing, Test Design, Test Scripts, Testing, Time Management, Willing to Travel, World Health Organization Drug Reference List (WHODrug), Writing Skills
LOCATION
Los Angeles, CA
POSTED
30+ days ago
Job Title: Drug Safety AnalystPay Rate: $42 - $45.7/hrLocation: Los Angeles, CAZIP Code: 90032Start Date: Right AwayKeywords: #LosAngelesjobs #DrugSafetyAnalystjobsBenefits: * Medical / Health Benefits with multiple plan options, Flexible Spending Accounts, Dental and Vision * 401k* On the job training / cross-training * Life Insurance, disability insurance* Voluntary life insurance for family members available. * Accident and critical illness insurance optional. * Scheduled performance reviews* Referral programJob DescriptionThis individual will provide operational support for global pharmacovigilance activities for investigational and marketed products. Ensures pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines. Responsible for data analysis and management obtained from the integrated database utilized by worldwide pharmacovigilance personnel. Responsible for project implementation and execution of system, including responsibilities for providing safety ongoing business support and ongoing improvements. Key interface with the IT system administrators to verify and test system changes, ensuring that the system is compliant and meets business needs.The personnel who cover the workplace will develop their activities according to the Pharmacovigilance System Master File (PSMF), Standard Operating Procedures (SOPs) and Working Practices (WPs) and following the Pharmacovigilance legislation.Responsibilities:Coordinate and participate in the safety data analysis, review, processing and evaluation in order to prepare aggrega1. Process and review safety data to develop aggregate safety reports2. Support to respond to requests from regulatory agencies3. Coordinate and manage creation of queries for data extraction used in different PV documents4. Develop training documentation and/or work instructions to determine methods and procedures5. Work as Signal Analyst during signal management activities including extractions of signal detection reports ensuring document filing and archivingEnsure quality and compliance with the legal requirements for pharmacovigilance tasks and responsibilities:1. Take part in self-inspection visits, audits, inspections and in CAPAs management2. Coordination and management of aggregate safety reports submissions; notifies Regulatory Affairs and business partners accordingly3. Interact with Regulatory Affairs Department as it relates to aggregate safety documents required by Regulatory Authorities4. Review legislation to ensure compliance with local regulatory Authorities requirements5. Provide training to concerned persons based on the training plan and managing training documentation; archive documents according to prevailing standards6. Management of documentation describing PV applications use, which may include, but not limited to: SOPs, WP, User requirements, functional and/or technical specifications, process flow diagrams7. Lead change management actions to assure PV team smoothly adapts to the new processes, as well as supporting the integration of a new application8. Gathering, prioritizing, and planning improvements based on user requests, taking into account overall regulations to the businessPV data base operating activities:1. Provide support in the updates in the database configuration of submission rules to Regulatory Authorities2. Provide support in the updates in the database configuration of products and studies3. Support drug safety applications with business administration tasks. Key project team technical expert to deliver solutions that are cost effective, sustainable, and meet business requirementsScientific and medical literature review:1. Define with the Knowledge Services Department the strategy of scientific searches that are performed2. Review scientific literature and bibliographic search results and determine the actions necessary to be taken therewithExperience:Drug Safety Analyst should ensure their knowledge of pharmacovigilance practices; existing legislation, regulations and guidelines; medical coding and safety-data administration. Drug Safety Analyst should have a university degree in health sciences/ biosciences and additional training in IT or have a university degree in IT with additional training and/or experience in pharmacovigilance. At least 2 years of relevant experience in pharmacovigilance and 2 years of relevant experience in managing data bases, is usually required. Availability for international travelling when necessary is also required.Qualifications:- Bachelors degree in Health Sciences/ Biosciences and additional training in IT or have a university degree in IT with additional training and/or experience in pharmacovigilance. - At least 2 years of relevant experience in pharmacovigilance and 2 years of relevant experience in managing data bases, is usually required. Availability for international travelling when necessary is also required.- Drug Safety Analyst should ensure their knowledge of pharmacovigilance practices; existing legislation, regulations and guidelines; medical coding and safety-data administration.- Proven Self-starter with strong work ethic and the ability to exercise good judgment.- Ability to work independently with minimum supervision.- Must be proactive, results oriented, and have strong attention to detail.- Strong organizational, analytical, and problem-solving skills with the ability to make structured decisions on a routine basis.- Strong interpersonal skills with the ability to interact and collaborate with personnel at all levels in a team environment.- Must possess strong technical writing and communication skills with ability to create and present design proposals, test scripts, execute training sessions and conduct effective meetings.- Ability to effectively prioritize and manage multiple tasks to ensure successful completion targeted deadlines-Proficient in Windows 7 and MS Office (Excel, PowerPoint, Visio, Word)- Familiarity with validation of computer systems and/or GMP environments is essential.- Knowledge of E2b (R2) and E2b (R3) is beneficial. Familiarity with Medical terminology, MedDRA, WhoDrug is beneficial- Familiarity with reporting tools such as Business Objects is strongly preferred.If you are interested in this role, please apply via the apply now link provided. Our overriding goal is to provide quality staffing solutions that help people, organizations, and communities succeed. Belcan is a leading provider of qualified personnel to many of the world's most respected enterprises. We offer excellent opportunities for contract, temporary, temp-to-hire, and direct assignments. We are the employer of choice for thousands worldwide. For more information, please visit our website at Belcan.comBelcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.

About the Company

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Belcan