Pv Professional

3-4 years

Not Disclosed

Bangalore

10 Sept. 11, 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, 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, our mission is to make good health more affordable and accessible, helping millions around the world lead healthier lives. With operations in nearly 60 countries and a diverse range of nationalities and backgrounds, we are the world's leading manufacturer of generic medicines and a proud producer of many products listed on the World Health Organization’s Essential Medicines List. Every day, at least 200 million people take one of our medicines. We are continually seeking new ways to make a difference and new people to join us in this mission.

How You'll Spend Your Day

Literature Review: Participate in literature review activities, designing and implementing comprehensive search strategies on specific products. Utilize databases such as Embase, Medline, Pubmed, and Ovid.
Regulatory Impact Assessment: Evaluate the impact of regulatory changes on current processes and contribute to process simplification.
Teva Portfolio Expertise: Apply knowledge and expertise related to Teva's product portfolio.
Pharmacovigilance Support: Assist pharmacovigilance teams with case processing, training, quality assurance, audits, and inspections.
Consultation and Communication: Serve as a consultant or Single Point of Contact (SPOC) for various case-related activities and maintain a knowledge repository of process updates and regulatory changes. Ensure effective communication with internal and external stakeholders to maintain transparency.
Data Analysis: Analyze quality data for trends and prepare the team for process stabilization. Ensure compliance with internal reporting key performance indicators.
Independent Operations: Interpret and make valuable decisions based on evolving regulatory requirements.
Training and Mentoring: Lead workshops, training sessions, and educational activities for process improvements. Mentor new hires with case processing knowledge and evaluate their progress.
Support and Other Tasks: Provide analytical support for investigations and audits, and perform additional tasks as assigned by the direct manager.

Your Experience and Qualifications

Educational Background: A graduate in life sciences, pharmaceuticals, or healthcare (B. Pharmacy, M. Pharmacy, Pharm D, BDS).
Experience: Minimum of 3-4 years in pharmacovigilance, including literature review processes and ICSR. Solid knowledge of pharmacovigilance concepts, regulations, and procedures.
Technical Skills: Advanced proficiency in Microsoft Office platforms.
Flexibility: Ability to adapt to shifting team priorities.
Communication Skills: Excellent written, verbal, and non-verbal communication skills.
Interpersonal Skills: Strong interpersonal and people skills, with good analytical and problem-solving abilities.

Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to providing equal employment opportunities without regard to 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 entitled to protection under applicable laws. We are dedicated to fostering a diverse and inclusive workplace. If you require accommodations during the recruitment and selection process, please let us know, and we will ensure that your needs are met confidentially.

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