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Pv Professional

3-4 years
Not Disclosed
10 July 29, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, 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 dedicated to making good health more affordable and accessible, striving to help millions worldwide enjoy healthier lives. Our mission unites people across nearly 60 countries, encompassing a diverse array of nationalities and backgrounds. As the world's leading manufacturer of generic medicines and the proud producer of numerous products on the World Health Organization’s Essential Medicines List, we impact the lives of at least 200 million people daily. We are continually seeking innovative ways to make a difference and invite new talent to join us in our mission.

Your Role

As a member of our team, you will:

  • Literature Review: Participate in literature review activities by designing and implementing comprehensive search strategies using databases such as Embase, Medline, PubMed, and Ovid.

  • Regulatory Impact Assessment: Assess the impact of regulatory changes on current processes and contribute to process simplification.

  • Pharmacovigilance Support: Support pharmacovigilance teams in case processing, training, quality assurance, audits, and inspections.

  • Consulting & Knowledge Management: Act as a consultant or Single Point of Contact (SPOC) for case-related activities and maintain a knowledge repository of process updates and regulatory changes.

  • Effective Communication: Maintain effective communication with internal departments and external stakeholders to ensure process transparency.

  • Data Analysis & Quality: Analyze quality data for trends and prepare the team for process stabilization while ensuring regulatory compliance by meeting key performance indicators.

  • Independent Initiatives: Operate independently and make valuable decisions in response to dynamic regulatory requirements.

  • Training & Mentoring: Conduct workshops, training sessions, and other interactive activities to educate the team on process improvements and error trends. Mentor new hires in case processing and evaluate their progress.

  • Additional Tasks: Perform other tasks as assigned by the direct manager.

Qualifications

  • Educational Background: Bachelor's or higher degree in life sciences, pharmaceutical, or healthcare fields (e.g., B. Pharmacy, M. Pharmacy, Pharm D, BDS).

  • Experience: Minimum of 3-4 years in pharmacovigilance with a focus on literature review processes in Individual Case Safety Reports (ICSR).

  • Expertise: Solid knowledge of pharmacovigilance concepts, regulations, and procedures, along with advanced proficiency in Microsoft Office.

  • Skills: Excellent communication (written, verbal, and non-verbal), interpersonal, analytical, and problem-solving skills. Ability to adapt to shifting team priorities.

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to providing equal employment opportunities regardless of age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin, or any other legally recognized status protected under applicable laws. We are dedicated to fostering a diverse and inclusive workplace. If you require accommodations during the recruitment process, please inform us, and we will ensure your needs are met confidentially.