<p><b>Job Title: </b>Safety Reporting Specialist</p> <p><b>Job Location: </b>Remote, India</p> <p><b>Job Location Type: </b>Remote</p> <p><b>Job Contract Type: </b>Full-time</p> <p><b>Job Seniority Level: </b></p><p style="text-align:left"><b>Work Schedule</b></p>Standard (Mon-Fri)<p style="text-align:inherit"></p><p style="text-align:left"><b>Environmental Conditions</b></p>Office<p style="text-align:inherit"></p><p style="text-align:left"><b><u>Job Description</u></b></p><p style="text-align:inherit"></p>Join us as Safety Reporting Specialist – To manage and coordinate the production of regulatory and safety reports, ensure accurate and timely documentation of adverse events, and support compliance with global pharmacovigilance requirements.<br/><br/>What You’ll Do:<br/>• Receive, prepare and submit safety reports to applicable parties. Escalate to lead and/or line manager if any issues are encountered. Ensure reports are <br/>submitted in compliance with regulatory timelines and country legislation. <br/>• Assist in producing metrics and alerts managers to any quality or timeline issues. <br/>• Participate in project teams and may lead projects of small to moderate scope. <br/>• Provide training and support for other team members. <br/>• Perform administrative tasks such as filing and the maintenance of safety reporting systems and information. <br/>• Liaise with various departments around safety reporting tasks and the setting up of client accounts. <br/>• Participating in audits where required and performing testing activities as needed. <br/>• Share ideas and suggestions with team members ensuring effective communication and participates in process improvement initiatives.<br/><br/>Education and Experience: <br/>• Bachelor's degree or equivalent and relevant formal academic / vocational qualification <br/>• Previous experience to provide the knowledge, skills, and abilities to perform the job (comparable to 2+ years’). <br/><br/>In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role. <br/><br/>Knowledge, Skills and Abilities: <br/>• Strong knowledge of medical terminology <br/>• Good written and verbal communication skills <br/>• Good Microsoft Word and Excel skills and solid understanding of safety database functionality <br/>• Solid knowledge of procedural documents and working knowledge of global safety reporting requirements (including FDA regulations and guidelines) <br/>• Ability to juggle multiple tasks while still delivering high quality results <br/>• Strong attention to detail and accuracy with orientation toward careful and meticulous work <br/>• Possess the maturity to handle sensitive information and data effectively <br/>• Ability to interact effectively with all levels of the organization <br/>• Strong critical thinking and problem-solving skills<br/><br/>Working Conditions and Environment: <br/>• Work is performed in an office/ laboratory and/or a clinical environment. <br/>• Exposure to biological fluids with potential exposure to infectious organisms. <br/>• Exposure to electrical office equipment. <br/>• Personal protective equipment required such as protective eyewear, garments and gloves.<br/><br/>Physical Requirements: <br/>• Ability to work in an upright and /or stationary position for 6-8 hours per day. <br/>• Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists. <br/>• Frequent mobility required. <br/>• Occasional crouching, stooping, with frequent bending and twisting of upper body and neck. <br/>• Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs. <br/>• Ability to access and use a variety of computer software developed both in-house and off-the-shelf. <br/>• Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. <br/>• Frequently interacts with others to obtain or relate information to diverse groups. <br/>• Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task. <br/>• Regular and consistent attendance.<br/><br/>Why Join Us?<br/>When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.<br/><br/>Apply today to help us deliver tomorrow’s breakthrough. <br/><p></p><p></p><p></p><p></p><br><br><p><strong>This job is curated by Lifelancer.</strong></p> <p><strong>Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. 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