Company Overview

Pharma Stuff, a leading pharmaceutical manufacturing company, is dedicated to innovation and quality in the production of life-saving drugs. With headquarters in Vijayawada, our firm employs over 1000 professionals focused on excellence. We nurture growth by promoting talented individuals from within our network and are proud of our strong presence in the Pharmaceutical Manufacturing industry.

Job Overview

Pharma Stuff is seeking a dedicated Drug Safety Associate Pharmacovigilance Trainee to join our team. This fresher-level role is ideal for individuals with 0 to 1 year of work experience. The position is available in multiple locations including Hyderabad, Pune, Bangalore Urban, Chennai, and Vijayawada and offers options for full-time, remote, internship, or freelance employment. This position requires skills in pharmacovigilance, clinical research, and clinical practices.

Qualifications and Skills

• A minimum of a bachelor's degree in pharmacy, life sciences, or a related field.
• Strong foundational knowledge in pharmacovigilance, focused on drug safety processes and protocols.
• Basic understanding of clinical research methodologies and practices.
• Ability to efficiently work in a team and independently, adapting to dynamic work environments.
• Attention to detail with strong organizational skills and ability to manage multiple tasks efficiently.
• Good communication skills, both written and verbal, essential for coordination and documentation.
• Proficiency in data entry and basic use of pharmacovigilance databases and reporting systems.
• Commitment to timelines, delivering results in a timely and efficient manner, crucial in pharmacovigilance roles.

Roles and Responsibilities

• Assist in the collection and reporting of adverse event data in compliance with pharmacovigilance standards.
• Support the pharmacovigilance team in monitoring drug safety and maintaining drug safety databases.
• Collaborate with cross-functional teams to ensure accurate documentation and reporting of safety information.
• Participate in training sessions to enhance understanding and implementation of safety regulation procedures.
• Conduct comprehensive reviews of clinical and post-marketing safety data related to company products.
• Contribute to the preparation and submission of safety reports to regulatory authorities as required.
• Maintain confidentiality and adhere to data protection guidelines when handling sensitive patient information.
• Continuously update knowledge on pharmacovigilance regulations and practices to support team objectives.