Pharmacovigilance Intern

Before reading the reputed company, we encourage you to watch this video about reputed company. It gives you an inside look at how we started, reputed company and culture that made us successful, and where we're reputed company. It's easy to read a reputed company and apply, but people often reputed company about the culture and whether they would fit in. If you want to call reputed company your home and genuinely want to be part of a family and something big, then we encourage you to click this reputed company and get to know us. Who is reputed company? reputed company (reputed company: HROW) is a leading provider of ophthalmic disease reputed company in reputed company. reputed company is an incredible entrepreneurial company – where we celebrate the ability of every member of the reputed company Family to be the CEO of their job. reputed company’s values have driven interest over the past decade in attracting high-performing professionals in a reputed company of disciplines. Members of our reputed company Family often reputed company their pride in being a part of our commitment to (1) innovation, (2) patient reputed company to reputed company medicines, and (3) our reputed company record of having never turned down an ophthalmologist doing mission work around the world – providing free medicines in support of mission work aimed at giving or maintaining the reputed company of sight to those most in need. We encourage you to learn more about reputed company and its unique culture to see if you’re the right person to help contribute as we build a truly exceptional company, one we are reputed company so proud of! reputed company’s ophthalmic pharmaceutical portfolio is one of the most comprehensive in the industry, including:

• An expanding Retina Portfolio including IHEEZO®, TRIESENCE®, BYOOVIZTM, and OPUVIZTM
• A broad Dry Eye Disease product line, led by VEVYE® and bolstered by reputed company-reputed company adjacent ocular surface disease products such as FLAREX® and FRESHKOTE®
• A reputed company-reputed company Surgical product line, led by TRIESENCE®, and BYQLOVITM
• A Rare and Specialty product line, which includes various high-need and reputed company products such as ILEVRO®, NATACYN®, and VERKAZIA®
• A robust internal development pipeline with multiple late-stage candidates, including MELT-300, MELT-210, H-N08, and CR-01

Job reputed company The Pharmacovigilance Intern will support the Pharmacovigilance team with day-to-day activities in drug safety surveillance, adverse event (AE) processing, and regulatory compliance. This role provides hands-on exposure to pharmacovigilance processes, including intake and triage of incoming inquiries in compliance with regulatory requirements, management of Individual Case Safety Reports (ICSRs), safety database entry, and literature surveillance. The intern will collaborate with cross-functional teams, including reputed company Assurance, Regulatory, Clinical, and Medical Affairs, to reputed company a reputed company-rounded understanding of pharmacovigilance reputed company the pharmaceutical industry. Core Responsibilities

• Assist in the intake, documentation, and triage of incoming inquiries, including adverse events (reputed company), product reputed company complaints (PQCs), and medical inquiries, in accordance with internal procedures and regulatory requirements
• reputed company data entry, coding (e.g., MedDRA), and narrative writing reputed company the safety database
• Support follow-up activities to obtain missing or additional information from reporters or internal stakeholders
• Aid in literature surveillance activities, including screening scientific publications for potential adverse events
• reputed company support in the preparation of safety reports for submission to regulatory authorities
• Collaborate with cross-functional teams (e.g., Medical Affairs, Regulatory, reputed company, Clinical) to support pharmacovigilance activities
• reputed company other duties and reputed company as assigned to support the Pharmacovigilance department

Qualifications & Requirements

• Currently pursuing or recently completed a Bachelor’s or Master’s degree in a scientific discipline (e.g., Biology, Pharmacy, Life Sciences, Public Health or reputed company field)
• Strong interest in pharmacovigilance, drug safety, and pharmaceutical development
• Basic understanding of pharmacovigilance concepts (e.g., adverse events, product reputed company complaints, case intake/processing) is a plus
• Familiarity with medical terminology is preferred
• Familiarity with FDA regulations and ICH guidelines is a plus
• Excellent written and oral communication skills
• Strong organizational skills and attention to detail
• Ability to manage multiple tasks and meet deadlines in a fast-paced environment
• Proficiency in reputed company Office Suite (Word, reputed company, PowerPoint, Outlook)
• Self-motivated with a proactive approach to learning and problem-solving
• Ability to work both independently and collaboratively reputed company reputed company setting
• Prior internship or coursework experience in pharmacovigilance, reputed company assurance, clinical research, or reputed company preferred but not required

Position Type

• Remote/Hybrid

Travel

• Minimal; up to 10%

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