Sitero is an emerging leader in clinical services and software solutions for the life sciences industry. We bring extensive experience across diverse therapeutic areas, focusing on innovative, technology-enabled solutions that allow our clients to concentrate on their core strengths. Our experienced team provides high-touch services and technology for early phase studies through Phase III clinical trials, ensuring the safety of all stakeholders in the clinical research community, with an emphasis on ethics, compliance, and innovation.
Location: Mysore
Function: Drug Safety
The Drug Safety Associate (DSA) is a safety professional responsible for assessing the safety of pharmaceutical drugs during clinical trials and in the market. Using standard guidelines, the DSA determines whether medications cause adverse reactions in patients and reports findings to regulatory bodies and health authorities.
As part of a dedicated team of safety professionals at Sitero, the DSA will collaborate closely with safety teams in Contract Research Organizations (CROs) and partners. This role requires maintaining medical knowledge, strong familiarity with drug safety and pharmacovigilance regulations, and expertise in safety surveillance and risk management.
Sitero offers a competitive compensation package, including a competitive salary, variable pay, paid time off, and healthcare and retirement benefits.
Full Time, Permanent
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