Pharmacovigilance Job at ProPharma: Apply now for an Intern Role
Looking for a pharmacovigilance job in India? ProPharma is offering an exciting Pharmacovigilance Intern opportunity in Hyderabad for candidates with Argus safety database experience. This role provides hands-on exposure to drug safety processes, case management, and regulatory reporting within a global pharmacovigilance environment.
Job Details:
- Job Position: Pharmacovigilance Intern
- Location: Hyderabad, India
- Duration: 12 Months
- Department: Pharmacovigilance
- Job ID: JR 7887
About the Company:
For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate partners’ most high-profile drug and device programs.
Job Description:
We are offering an exciting internship opportunity in the Pharmacovigilance department for individuals with experience in the Argus safety database. This pharmacovigilance job will provide hands-on experience in drug safety processes, case management, and regulatory reporting, helping interns build a strong foundation in pharmacovigilance.
Qualifications:
- Completed a degree in Medicine or a related field.
- Basic knowledge and prior training/experience with the Argus safety database are required.
- Understanding of pharmacovigilance principles and drug safety regulations.
- Strong attention to detail, analytical skills, and ability to work in a fast-paced environment.
- Proficiency in Microsoft Office (Word, Excel, PowerPoint).
- Strong verbal, written, and interpersonal communication skills.
Key Responsibilities:
- Manage assigned mailboxes, including inbox triage of client communication, inbound reports, and internal case processing communications.
- Perform duplicate searches and complete initial book-in as required.
- Enter basic data into the safety database, such as the identifiable patient, report, suspect drug, and adverse event.
- Assist in case processing within the Argus database, including follow-ups.
- Assist in narrative writing and MedDRA coding.
- Support in Individual Case Safety Report (ICSR) management, ensuring compliance with regulatory requirements.
- Work with cross-functional teams to ensure timely adverse event reporting.
- Maintain accurate documentation and adhere to pharmacovigilance compliance standards.
