Instagram
youtube
Facebook

Pv Professional

3-4 years
Prefered by Company
10 Nov. 20, 2024
Job Description
Job Type: Full Time Education: life sciences/pharmaceutical/healthcare professional graduate (B. Pharmacy, M. Pharmacy, Pharm D, BDS) Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

About Us

At Teva Pharmaceuticals, we are united by a mission to make good health more affordable and accessible to millions worldwide. Our global presence spans nearly 60 countries, and our diverse team works across a wide range of nationalities and backgrounds. As the world’s leading manufacturer of generic medicines, we proudly produce many products featured on the World Health Organization’s Essential Medicines List. Today, over 200 million people around the world rely on our medicines every day, but our commitment to improving healthcare continues. We’re always seeking innovative ways to make a difference—and we need new people to help us achieve that goal.


Your Role

As a key member of our Pharmacovigilance team, you will play an important role in patient safety, ensuring that we meet the highest standards in case processing, regulatory compliance, and process improvement. You will engage in a variety of activities, including literature reviews, regulatory assessments, and supporting training, audits, and inspections.


Key Responsibilities

  • Literature Review & Data Analysis

    • Design and implement comprehensive literature search strategies for specific products using databases such as Embase, Medline, PubMed, Ovid, etc.
    • Analyze and assess trends in data to help stabilize processes and improve overall quality.
  • Regulatory Compliance & Process Improvement

    • Assess the impact of regulatory changes on current processes and contribute to their simplification.
    • Ensure compliance with regulatory requirements and meet internal reporting Key Performance Indicators (KPIs).
    • Maintain an up-to-date repository of process updates and regulatory changes, acting as a Subject Matter Expert (SME) or Single Point of Contact (SPOC) for case-related activities.
  • Stakeholder Communication & Collaboration

    • Foster effective communication with internal teams (e.g., related departments) and external stakeholders (e.g., partners, authorities, vendors) to ensure transparency in processes.
  • Training & Mentorship

    • Conduct workshops, training sessions, and other interactive activities to educate the team on existing and emerging trends for process improvement.
    • Mentor new hires through knowledge transfer and evaluate their progress, guiding them towards achieving excellence in case processing.
  • Operational Excellence & Independent Initiative

    • Take ownership of independent operations, making informed decisions in response to changing regulatory requirements.
    • Be actively involved in team transitions, ensuring that teams are certified and properly equipped.
  • Audit & Inspection Support

    • Provide analytical support for peer investigations and trend analysis, contributing to audits and inspections.
  • Additional Responsibilities

    • Perform other tasks as assigned by your direct manager.

Your Qualifications & Experience

  • Educational Background: A degree in Life Sciences, Pharmacy, Healthcare, or a related field (e.g., B. Pharmacy, M. Pharmacy, Pharm D, BDS).

  • Professional Experience:

    • 3-4 years of experience in Pharmacovigilance, with specific knowledge in literature review processes for Individual Case Safety Reports (ICSRs).
    • Solid understanding of patient safety, pharmacovigilance concepts, regulations, and procedures.
  • Skills & Competencies:

    • Advanced proficiency in Microsoft Office (Excel, Word, PowerPoint, etc.).
    • Strong analytical and problem-solving skills.
    • Excellent communication skills (written, verbal, non-verbal).
    • Interpersonal skills with the ability to work collaboratively across teams.
    • Adaptability to shifting priorities in a dynamic environment.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. We ensure that all applicants receive fair treatment regardless of age, race, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin, or any other legally protected status.

We are committed to fostering a diverse and inclusive workplace. If you require accommodations during the recruitment process, please inform us so we can provide a supportive and accessible candidate experience.