Job Summary
We are seeking a Subject Matter Expert in Pharmacovigilance with 2 to 4 years of experience to join our team. The ideal candidate will have a strong background in Pharma Research & Development and a keen interest in PV data management and case processing. This hybrid role offers the opportunity to work in a dynamic environment contributing to the safety and efficacy of pharmaceutical products.
Responsibilities
Conduct thorough analysis of pharmacovigilance data to ensure compliance with regulatory standards and enhance drug safety.Collaborate with cross-functional teams to support the development and implementation of pharmacovigilance strategies.Provide expert guidance on PV case processing to ensure accurate and timely reporting of adverse events.Utilize technical skills in Pharma Research & Development to drive innovation and improve pharmacovigilance processes.Monitor and evaluate the effectiveness of pharmacovigilance systems and recommend improvements.Develop and maintain comprehensive documentation of pharmacovigilance activities and findings.Assist in the preparation of regulatory submissions and safety reports to ensure compliance with global standards.Engage in continuous learning to stay updated on the latest trends and advancements in pharmacovigilance.Support the training and development of team members to enhance overall team performance.Ensure data integrity and accuracy in all pharmacovigilance activities to maintain high-quality standards.Participate in audits and inspections to demonstrate compliance with regulatory requirements.Foster a culture of safety and vigilance within the organization to protect public health.Contribute to the companys mission by ensuring the safe and effective use of pharmaceutical products.
Qualifications
Possess a strong foundation in Pharma Research & Development essential for driving pharmacovigilance initiatives.Demonstrate expertise in PV data management and case processing enhancing the quality of safety assessments.Exhibit excellent analytical skills to interpret complex pharmacovigilance data and derive actionable insights.Show proficiency in regulatory compliance ensuring adherence to global pharmacovigilance standards.Display effective communication skills to collaborate with cross-functional teams and stakeholders.Maintain a proactive approach to problem-solving ensuring timely resolution of pharmacovigilance issues.
Certifications Required
Certified Pharmacovigilance Professional (CPP) or equivalent certification preferred.
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。
