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Fortrea

Global CRO providing Phase I-IV trials

Lead Safety Systems Specialist

Enterprise ApplicationsConfirmed live in the last 24 hours
Full-timeBengaluru, Karnataka, IndiaNo salary listed

About the Job

Requirements

  • A Life Science or IT/computing degree, although relevant and equivalent experience may be considered in lieu of the educational requirement.
  • Experience in a systems operations support role.
  • Experience working on validated document management systems.
  • At least 4 years of experience with drug safety systems such as Argus, ARISg, or Veeva.
  • Good working knowledge of Microsoft Office tools.
  • Knowledge of system integration.
  • Ability to set priorities and handle multiple tasks.
  • Attention to detail.
  • Good written and verbal communication skills.
  • Logical and spelling skills, preferably with an aptitude for handling and proofreading numerical data.
  • Ability to operate standard office equipment.

Responsibilities

  • Assist with overall safety system implementation, support, configuration, and migration activities, providing services to clients through client project groups or as a standalone business.
  • Provide internal and external clients with quality service in a safe and cost-effective manner.
  • Leverage business and technical knowledge as a pharmacovigilance systems expert.
  • Conduct project-specific configurations in safety systems.
  • Maintain and document system configurations based on initial requirements and subsequent changes.
  • Evaluate proposed project ideas and software changes through technical impact analysis and estimated business value to contribute to decision-making.
  • Develop and document standard and ad hoc reports from safety systems.
  • Support and educate end users and sponsors, where applicable.
  • Collaborate with the training team to develop safety-system-specific training modules.
  • Discuss business needs with stakeholders, document user requirements, and ensure timely delivery in collaboration with the technology partner.
  • Guide and strategize the use of standard safety systems front-end reporting, including advanced conditions and Standard MedDRA Queries.
  • Conduct routine and ad hoc data extraction, including PSURs, DSURs, and six-monthly listings.
  • Participate in data migration activities and related documentation.
  • Support system change management and training as needed.
  • Manage tickets, resolve issues, and escalate system issues where applicable.
  • Respond to mailbox queries and monitor the mailbox for system failures, resolving them in a timely manner.
  • Manage vendors.
  • Train team members on technical and functional aspects.
  • Complete assignments to high quality standards, adhere to relevant standard operating procedures, and keep current with pharmacovigilance regulations.
  • Update departmental standard operating procedures, working practices, and guidelines.
  • Act as a subject matter expert and identify improvements to compliance, quality, and efficiency.
  • Perform user acceptance testing and complete required documentation.
  • Lead critical team projects and manage the team's workload.
  • Perform other duties as assigned.

Desired Qualifications

  • Knowledge of Microsoft Office and Windows.
  • Clinical background working with clinical systems.
  • Understanding of SQL programming language.
  • Experience working with ticket support applications.

About the Company

Fortrea

Global CRO providing Phase I-IV trials

Fortrea is a global contract research organization that provides clinical development services for the life sciences industry. It offers full service, functional service, and hybrid outsourcing models across Phase I–IV trials, clinical pharmacology, and consulting, serving biotech, biopharma, medical devices, and diagnostics. Its work is delivered through a network of investigators and specialized teams in approximately 100 countries, supporting trial design, execution, data management, and regulatory compliance. Fortrea’s approach combines its legacy experience from Covance and Labcorp with a pureplay CRO model to deliver fit-for-purpose solutions and agile project delivery. This positions it to manage trials across more than 20 therapeutic areas with scientific rigor and operational excellence. The company aims to bring predictability to clinical trial execution and help clients turn research ideas into real-world outcomes.

Company size
10,001+
Company stage
IPO
Headquarters
Winston-Salem, NC
Founded
2023

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