Drug Safety Specialist
Company: Selva Infosys LLC
- Location: Manchester, United States
- Work mode: On-site
- Seniority: Entry level
- Employment type: Full-time
- Posted: Yesterday
- Offer language: English
Job description
Company Description Selva Infosys LLC operates at the intersection of medical practice compliance and automated workflows for healthcare organizations. The company provides a complete financial lifecycle framework that reduces operational friction and improves process efficiency. Its solutions are designed to shorten turnaround times and help healthcare systems capture the full value of patient care. Team members collaborate with clinical and administrative stakeholders to support compliant, streamlined operations that enable better healthcare delivery.
Role Description The Drug Safety Specialist is a full-time, on-site role based in Manchester, NH. This position is responsible for monitoring, evaluating, and documenting adverse drug events and safety signals across supported healthcare environments. Day-to-day tasks include reviewing clinical and pharmacy data, performing risk assessments, maintaining safety documentation, and ensuring adherence to applicable regulatory requirements and company policies. The specialist will collaborate with physicians, pharmacists, and other healthcare professionals to support safe medication practices and contribute to the development of safety protocols and training materials. The role also involves preparing reports for internal and external stakeholders and participating in audits or inspections related to drug safety and compliance.
Qualifications
- Strong knowledge of regulatory requirements and regulatory affairs relevant to drug safety and healthcare compliance.
- Background in pharmacy and medicine, with the ability to interpret prescribing information, medication profiles, and clinical documentation.
- Experience with clinical trials or clinical research, including adverse event reporting and safety monitoring processes.
- Attention to detail, analytical skills, and ability to synthesize clinical and operational data into clear safety assessments and reports.
- Bachelor’s or advanced degree in Pharmacy, Medicine, Nursing, Public Health, or a related life sciences field.
- Familiarity with healthcare compliance frameworks, quality assurance practices, and electronic health records or safety databases.
- Effective written and verbal communication skills, with the ability to collaborate in multidisciplinary teams and interact with clinical and administrative stakeholders.
- Prior experience in pharmacovigilance, drug safety, or a related healthcare quality role is preferred.
