Employment Type: Full‑time
Location: Budapest
Shift Pattern: General daytime schedule
Work Arrangement: Primarily hybrid. Our team currently meets in the office 1 day per week.
We offer:
· Competitive salary and benefit package (cafeteria + annual bonus)
· Training and continuous learning and certification opportunities
· Free medical benefit package
· Reimbursable language courses
· Risk and accident insurance
· Chance to be part of a rapidly expanding organization
· Multilingual, multicultural environment with native colleagues
· All You Can Move SportPass (at a discounted price)
· Team events, company events
· Relocation package
· High value awards and recognitions
Your profile:
- Graduate in Pharmacy or Life Science
- 1 year of Pharmacovigilance or relevant clinical experience
- Min. B2 spoken and written Spanish and English proficiency
Key Responsibilities
- Responsible for receiving/downloading information from different channels and receiving voice calls for reporting safety information.
- Route information/safety reports to appropriate Department (e.g. medical information, quality assurance) as applicable.
- Monitoring mailbox, triage for patient safety reports and emails.
- Maintaining and archival of emails/source documents and updating shared folders.
- Handling of source document and entering data in front-end system as per triage criteria; acknowledge receipt of information.
- Obtain consent from reporter to follow up on safety reports.
- Assess cases for missing information and follow up attempts until closure.
- Check case validity.
- Perform initial checks, search database to prevent duplicate entries.
- Ensure upfront clarification requests in case of data discrepancy identified in source document.
- Enter safety information in front-end system and evaluating the safety information for case seriousness and potential upgrade and downgrade for seriousness in follow up cases, evaluate dechallenge-rechallenge.
- Translation & Back Translation of safety information as applicable.
- Anonymize/redact source documents and/or AE forms (as applicable).
- Responsible for receiving, reviewing and archiving source data records for any missing/discrepant safety information.
- Identify discrepancies and maintain email clarifications of discrepancies for SDV.
- Perform Health Authority database/registry extraction to retrieve and processes Individual Case Safety Reports.
- Document review processes.
- Responsible for completion of day-to-day work and process flows within the agreed SLAs
- Maintaining data as per customer guidelines.
- Work with project quality roles to improve case quality.
- Attend training sessions and develop skills and capabilities on an ongoing basis.
- Timely completion of assigned trainings and training files.
- Co-ordinate with internal teams to obtain necessary information required for day-to-day operations.
- Assists in the training and mentorship of new joiners as necessary.
CogHU103
私たちについて：
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として、AI投資を企業価値へとつなげるフルスタックのAIソリューションを提供しています。業界、業務プロセス、エンジニアリングに関する深い専門性を強みに、各企業固有のコンテキストをテクノロジーシステムに組み込み、人の力を最大限に引き出すとともに、具体的な成果の創出と、急速に変化する世界におけるグローバル企業の競争力維持を支援します。詳しくは、当社ウェブサイト www.cognizant.com 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。
