Pharmacovigilance Intern
ProPharma
Date: 18 hours ago
City: Hyderabad, Telangana
Contract type: Full time
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 our partners’ most high-profile drug and device programs.
Essential Functions
Post-secondary education.
Experience Requirements
Preferred: one year of industry experience.
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
Essential Functions
- 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.
- Screen and redact the source documents for PHI as per company procedures.
- Facilitate literature related activities as needed.
- Initial triage of regulatory authority database searches.
- Send draft reports to clients for review as needed.
- Enter basic data into safety database as required such as identifiable patient, report, suspect drug, and adverse event.
- As applicable perform full data entry into safety databased with proper experience and training.
- Other duties as assigned.
- Strong verbal, written and interpersonal communication skills.
- Proficient computer knowledge and computer keyboarding skills.
- Strong organization and prioritization skills, with strong attention to detail.
- Ability to work independently and within a team.
Post-secondary education.
Experience Requirements
Preferred: one year of industry experience.
We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.
All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***
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