Job Summary
Join our team as a Specialist in Pharmacovigilance where you will leverage your expertise in Pharma Research & Development to ensure the safety and efficacy of pharmaceutical products. With a focus on PV data management and case processing you will play a crucial role in monitoring and evaluating drug safety. This hybrid role offers a dynamic work environment with no travel required allowing you to contribute effectively during day shifts.
Responsibilities
- Monitor and evaluate drug safety data to ensure compliance with regulatory standards and company policies.
- Collaborate with cross-functional teams to analyze and interpret pharmacovigilance data for accurate reporting.
- Develop and implement strategies to enhance the efficiency of PV case processing and data management.
- Provide insights and recommendations based on data analysis to improve product safety and efficacy.
- Ensure timely and accurate documentation of adverse event reports and safety assessments.
- Assist in the preparation of regulatory submissions and safety reports to support product approvals.
- Conduct regular audits of PV processes to identify areas for improvement and ensure quality control.
- Facilitate training sessions for team members to enhance their understanding of pharmacovigilance practices.
- Utilize advanced tools and methodologies to streamline data collection and analysis processes.
- Coordinate with global teams to ensure consistency in pharmacovigilance operations and reporting.
- Support the development of risk management plans and safety monitoring strategies.
- Engage in continuous learning to stay updated with the latest industry trends and regulatory changes.
- Contribute to the companys mission of ensuring public health and safety through diligent pharmacovigilance practices. Qualifications
- Possess a strong background in Pharma Research & Development with hands-on experience in pharmacovigilance.
- Demonstrate expertise in PV data management and case processing showcasing a keen eye for detail.
- Exhibit excellent analytical skills to interpret complex data and provide actionable insights.
- Have a proactive approach to identifying and resolving issues related to drug safety.
- Show proficiency in using pharmacovigilance software and tools for efficient data handling.
- Display strong communication skills to collaborate effectively with cross-functional teams.
- Maintain a commitment to continuous learning and professional development in the field of pharmacovigilance.
Certifications Required
Certified Pharmacovigilance Professional (CPP) Advanced Pharmacovigilance Certification
コグニザントについて
コグニザント（NASDAQ: CTSH）は、AI Builderおよびテクノロジーサービスプロバイダーとして、お客様にフルスタックのAIソリューションを構築することで、AI投資と企業価値を結ぶ架け橋となっています。業界、ビジネスプロセス、エンジニアリングに関する当社の深い専門知識を活かし、組織固有のビジネス環境をテクノロジー・システムに組み込みます。これにより、人間の可能性を最大限に引き出し、確かな成果を実現するとともに、急速に変化する世界においてグローバル企業が常に一歩先を行くための支援を行っています。 詳細については、cognizant.ai をご覧ください。
雇用に関する追加情報
本募集に記載されている報酬情報は、掲載日時点で正確なものです。Cognizantは、適用される法令に従い、いつでも本情報を変更する権利を留保します。
応募者は、対面またはビデオ会議による面接への参加を求められる場合があります。また、各面接の際に、現在有効な州政府または政府発行の身分証明書の提示を求められる場合があります。
Cognizantは機会均等雇用主です。応募および選考において、人種、肌の色、性別、宗教、信条、性的指向、性自認、国籍、障がい、遺伝情報、妊娠、退役軍人の地位、その他連邦法・州法・地方自治体の法律により保護されるいかなる特性に基づく差別も行いません。
