Drug Safety Associate (Pharmacovigilance trainee)
🚀Hiring for Drug Safety Associate (Pharmacovigilance trainee)
Company Overview🌐:
i. Pharma Stuff is a leading pharmaceutical manufacturing company focused on innovation and quality in producing life-saving drugs.
ii. Headquartered in Vijayawada, the company employs over 1000 professionals committed to excellence.
iii. Pharma Stuff fosters internal growth by promoting talented individuals within its network.
iv. The company is recognized for its strong presence in the Pharmaceutical Manufacturing industry.
Job Overview
i. Pharma Stuff is looking for a Drug Safety Associate Pharmacovigilance Trainee to join the team.
ii. This entry-level position is suited for candidates with 0-1 year of experience.
iii. Locations include Hyderabad, Pune, Bangalore Urban, Chennai, and Vijayawada, with options for full-time, remote, internship, or freelance work.
iv. Skills required are pharmacovigilance, clinical research, and clinical practices.
🎓Qualifications and Skills:
i. A bachelor’s degree in pharmacy, life sciences, or a related field is required.
ii. Foundational knowledge in pharmacovigilance, especially in drug safety processes and protocols, is essential.
iii. Basic understanding of clinical research methodologies and practices is expected.
iv. Teamwork and independent working ability in a dynamic environment are necessary.
v. Strong organizational skills, attention to detail, and ability to manage multiple tasks are crucial.
vi. Good communication skills, both written and verbal, are essential for effective coordination and documentation.
vii. Proficiency in data entry and basic pharmacovigilance databases and reporting systems is required.
viii. Commitment to meeting deadlines is crucial in this pharmacovigilance role.
📌Roles and Responsibilities:
i. Assist in collecting and reporting adverse event data according to pharmacovigilance standards.
ii. Support the pharmacovigilance team in monitoring drug safety and maintaining databases.
iii. Collaborate with cross-functional teams to ensure accurate safety documentation and reporting.
iv. Participate in training sessions for understanding and implementing safety regulations.
v. Conduct reviews of clinical and post-marketing safety data for company products.
vi. Help prepare and submit safety reports to regulatory authorities as needed.
vii. Maintain confidentiality and follow data protection guidelines for handling patient information.
viii. Continuously update knowledge on pharmacovigilance regulations to support team objectives.
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