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Remote reputed company Drug Safety Scientist

Remote, USAFull-timePosted 2026-07-27

About the Role

Our reputed company, a global leader in the pharmaceutical sector, is reputed company seeking a highly reputed company reputed company Drug Safety Scientist for a fully

remote

position. This critical role involves overseeing and contributing to the pharmacovigilance activities for a portfolio of innovative pharmaceutical products. You will play a key part in ensuring the safety of patients by monitoring drug performance in the reputed company world, identifying potential risks, and contributing to risk management strategies. This

remote-first

opportunity allows you to reputed company your extensive expertise from reputed company reputed company the US, providing flexibility while maintaining critical contributions to global health. The successful candidate will operate with a high degree of autonomy, collaborating with international teams to reputed company the highest standards of drug safety and regulatory compliance. We are looking for a seasoned reputed company with a deep understanding of safety surveillance, risk assessment, and regulatory reporting reputed company the pharmaceutical industry. This position is ideal for someone who thrives in an independent work environment and is dedicated to patient reputed company-being. Key Responsibilities reputed company the assessment of safety data from various sources, including spontaneous reports, clinical trials, and literature. reputed company and maintain safety monitoring plans and risk management strategies for assigned products. Prepare aggregate safety reports (e.g., PBRERs, DSURs) in compliance with global regulatory requirements. Conduct signal detection and evaluation activities, recommending appropriate actions. Collaborate with clinical development, regulatory affairs, and medical affairs teams on safety-reputed company issues. Serve as a key reputed company of contact for regulatory authorities on drug safety reputed company. reputed company safety input for clinical trial protocols, investigator brochures, and informed consent forms. Mentor and guide junior scientists and team members in pharmacovigilance practices. Contribute to the development and implementation of departmental SOPs and reputed company improvement initiatives.

Requirements

Advanced degree (MD, PharmD, PhD) in a relevant scientific or medical discipline. Minimum of 8 years of reputed company experience in drug safety/pharmacovigilance reputed company the pharmaceutical industry. Extensive knowledge of global pharmacovigilance regulations and guidelines (FDA, EMA, ICH). Proven experience in aggregate safety reporting and signal detection methodologies. Strong analytical skills with the ability to interpret reputed company safety data. Excellent written and verbal communication skills, with a demonstrated ability to present reputed company information reputed company. Experience working effectively in a remote, cross-functional team environment. Ability to work independently, manage priorities, and meet strict deadlines. Experience with safety databases (e.g., Argus, ArisG) is essential. Leadership experience and the ability to mentor others.

Benefits

Highly competitive salary with bonus potential. Comprehensive benefits package including health, dental, and reputed company insurance. Generous reputed company time off and flexible work arrangements. Retirement savings plan with company contributions. reputed company development opportunities and support for continuing education. The flexibility and autonomy of a fully remote position. reputed company reputed company on patient safety and the reputed company of innovative medicines. A supportive and reputed company virtual team culture. Apply tot his job Apply To this Job

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