FSP Pharmacovigilance Coordinator – Night Shift
Posted 25 days ago
You'll complete your application on Thermo Fisher Scientific's career site.
About the Role
This role is for a night-shift Pharmacovigilance Coordinator focused on advancing life science research and health outcomes. Working within a worldwide, cooperative group, you will maintain the integrity, regulatory compliance, and audit readiness of safety programs to support the creation of innovative medical treatments. Operating in a flexible, virtual setting, you will oversee intricate project logistics and data organization. You will serve as a vital link between clients, board members, and project staff, ensuring all safety matters and communications are addressed accurately. Through managing records, monitoring project information, and assisting office operations, you will contribute significantly to the progress of global scientific projects.
Requirements
- You must hold a high school diploma or equivalent, plus a pertinent vocational or academic degree.
- You need a minimum of two years of professional experience relevant to the position's requirements.
- You must be skilled in using Microsoft Office tools, specifically PowerPoint, Word, Access, and Excel.
- You should have strong communication and interpersonal abilities, a talent for problem-solving, and the capacity to function autonomously with little oversight.
- You need to demonstrate extreme precision and the ability to juggle numerous responsibilities under firm time constraints.
- You must have a firm grasp of ICH Good Clinical Practices, FDA mandates, and internal operating procedures.
- You must be prepared to work night shifts and show adaptability when project schedules evolve.
Responsibilities
- You will manage the punctual evaluation of adverse events and protocol questions, while tracking data and producing comprehensive reports for interested parties.
- You will organize logistics for national and international committee meetings and produce key legal documents, such as member and confidentiality contracts.
- You will assemble adjudication files, ensure project records remain current and prepared for audits, and support meetings by recording minutes and disseminating documents.
- You will conduct data entry, track budgets and expenditures, coordinate translations, and offer guidance to less experienced team members.
- You will remove personal subject information to protect data privacy.
- You will act as the primary contact to maintain professional and tactful interactions among external vendors, clients, and internal staff.
Benefits & Perks
- This is a full-time, completely remote position with a Monday to Friday working schedule.
- You will receive continuous professional development and training, with opportunities to mentor and instruct junior staff.
Note: This listing is summarized and paraphrased by WorkNow from a publicly posted role. For the original wording and full details, please refer to the employer's official posting.
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