Remote Pharmacovigilance Jobs at Thermo Fisher Scientific

Work from Home Pharmacovigilance Jobs at Thermo Fisher as a Safety Specialist

In the rapidly evolving landscape of pharmacovigilance, Thermo Fisher Scientific offers an exciting opportunity for professionals to work from home as Safety Specialists. Explore the details of this unique position and learn how you can contribute to groundbreaking clinical research from the comfort of your home

Thermo Fisher Scientific, a leading global contract research organization (CRO), is actively seeking qualified candidates for full-time remote positions in clinical research. Dive into the specifics of the Safety Specialist role, its responsibilities, and the incredible impact it has on bringing life-changing drugs to market.

About Thermo Fisher Scientific:

Thermo Fisher Scientific, a pioneer in clinical research services, is dedicated to developing drugs that address the world’s most challenging health concerns. Join our team and be part of the leading global CRO powering the PPD® clinical research portfolio.

Thermo Fisher Scientific Vacancies:

Explore the available opportunities to join our dynamic team:

Job Description:

As a Safety Specialist working from home, you will play a vital role in performing day-to-day pharmacovigilance (PV) activities within a highly regulated environment. Your responsibilities will include:

• Collection, monitoring, assessment, evaluation, research, and tracking of safety information.
• Coordination and performance of PV activities such as data entry, coding, and adverse event assessment.
• Regulatory reporting activities and collaboration with project team members, client contacts, investigators, and third-party vendors.

About the Department & Responsibilities:

As a key member of our Clinical Research team, you will:

• Works independently to perform day-to-day PV activities. May participate in on[1]call duties for specific projects to ensure 24-hr coverage for intake of cases from investigative sites.
• Operates in a lead capacity. Provides assistance in the development of program and departmental procedural documents. May prepare for and attend audits. Mentors less expert staff. Reviews regulatory/pharmacovigilance publications and information sources t
• 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.
• Responsible for routine project implementation and coordination (e.g., Clinical Trials, Endpoint Assessment Committee/Data Safety Monitoring Committee), including presentations at client/investigator meetings, and review of metrics and budget considerations.

Educational and Experience Requirements:

• Education and Experience:

  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 5+ years).

  Knowledge, Skills and Abilities:

  • Thorough understanding of pathophysiology and the disease process
  • Solid understanding of relevant therapeutic areas as the need arises for processing AEs
  • Excellent critical thinking and problem solving skills with ability to evaluate and escalate appropriately
  • Proficient at sophisticated clinical study administration including budget activities and forecasting
  • Excellent 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
  • Proficient in Microsoft Office products (including Outlook, Word, and Excel)
  • Thorough understanding of the global regulatory requirements and 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 exciting circumstances
  • Ability to work effectively within a team to attain a shared goal

How to Apply:

To apply for the position of Safety Specialist at Thermo Fisher Scientific, please submit your application here. Include your resume, cover letter, and any additional documents that showcase your qualifications and experience.

Apply here