ThermoFisher Scientific announced job vacancy for the post of FSP – Associate Safety Specialist. The place of posting will be at Remote (Work from Home). Candidates who have completed Bachelor’s degree or equivalent and relevant formal academic / vocational qualification with 0 – 2 Years of Experience are eligible to apply. More details about qualifications, job description and roles & responsibilities are as follows
Company Overview
| Name of the Company | ThermoFisher Scientific |
| Required Qualifications | Graduate |
| Skills | Strong critical thinking and problem-solving skills |
| Category | Clinical Research |
| Work Type | Remote |
As part of their expert team, you’ll have the opportunity to ensure operational excellence that makes a real difference in patient safety. As Associate Safety Specialist, you’ll perform day-to-day Pharmacovigilance (PV) activities within a highly regulated environment driven by strict timelines. Your responsibilities will include, but are not limited to, the collection, monitoring, assessment, evaluation, research, and tracking of safety information. You will perform activities such as adverse event data entry, coding, assessment of adverse events, case review, follow-up, tracking of reports, and regulatory reporting activities. You will effectively collaborate with various parties such as project team members, client contacts, investigators, adverse event reporters, and third-party vendors.
Job Details
Θ Positions: FSP – Associate Safety Specialist
Θ Job Location: Remote (Work from Home)
Θ Salary: As per company standards
Θ Job Type: Full Time
Θ Requisition ID: R-01363423
Roles and Responsibilities:
- Performs day-to-day PV activities. May participate in on-call duties for specific projects to ensure 24-hr coverage for intake of cases from investigative sites.
- Reviews regulatory/pharmacovigilance publications and information sources to keep updated on current regulations, practices, procedures and proposals. Maintains medical understanding of applicable therapeutic area and disease states.
- Reviews cases entered for quality, consistency and accuracy, including review of peer reports.
- Prepares and maintains regulatory safety reports.
Required Skills & Qualifications:
- Bachelor’s degree or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).
- Strong critical thinking and problem-solving skills
- Good oral and written communication skills including paraphrasing skills
- Good command of English and ability to translate information into local language where required
- Computer literate with the ability to work within multiple databases
- Previous exposure to Microsoft Office packages (including Outlook, Word, and Excel)
- Understanding of medical terminology
- Understanding the importance of and compliance with procedural documents and regulations
- Ability to manage and prioritize a variety of tasks and meet strict deadlines with limited supervision
- Strong attention to detail
- Ability to maintain a positive and professional demeanor in challenging circumstances
- Ability to work effectively within a team to attain a shared goal
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