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IQVIA

Runs drug trials and sells health data to pharma

PV Specialist

Biology & BiotechPosted on Nov 4
Full-timeNo salary listed

About the Job

Requirements

  • A minimum of a Bachelor's degree in a scientific or healthcare discipline or allied life sciences, with 1–1.5 years of relevant experience.
  • Good knowledge of medical terminology.
  • Working knowledge of the applicable safety database.
  • Knowledge of applicable global, regional, and local clinical research regulatory requirements.
  • Attention to detail and accuracy.
  • Working knowledge of Microsoft Office and web-based applications.
  • Organizational and time-management skills.
  • Verbal and written communication skills.
  • Ability to follow instructions and guidelines, use initiative, and work independently.
  • Ability to multitask and manage competing priorities and deadlines.
  • Ability to delegate to less experienced team members.
  • Ability to establish and maintain effective communication and working relationships with coworkers, managers, and clients.
  • Ability to ensure deliverable quality according to agreed terms.
  • Ability to use the telephone and communicate face-to-face with accurate perception of speech.
  • Ability to sit regularly for extended periods.
  • Willingness and aptitude to learn new skills across Safety service lines.
  • Flexibility to operate in shifts.

Responsibilities

  • Prioritize and complete assigned training on time.
  • Process safety data according to applicable regulations, guidelines, standard operating procedures, and project requirements.
  • Perform pharmacovigilance activities as required by the project, including collecting and tracking incoming adverse events and endpoint information, determining initial or update status of incoming events, entering data into databases, coding adverse events and products, writing narratives, and conducting literature-related activities within internal and project timelines.
  • Meet quality, productivity, and delivery standards for project requirements.
  • Ensure compliance with project-related processes and activities.
  • Create, maintain, and track cases as applicable to the project plan.
  • Identify quality problems and bring them to the attention of a senior team member.
  • Attend project team meetings and provide feedback to the operations manager on challenges, issues, or successes.
  • Comply with people practices and processes.
  • Perform other duties as assigned.

Desired Qualifications

  • Self-motivation and flexibility.
  • Ability to demonstrate problem-solving capabilities.
  • Ability to work as a team player, contribute to team goals, and work effectively with others.
  • Demonstration of IQVIA core values in daily tasks.
  • Willingness to travel occasionally.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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