Medical Safety Analyst

at  AbbVie

Company Description
AbbVie’s mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people’s lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.
Job Description

EDUCATION AND EXPERIENCE:

• Possess a university degree in a health/life sciences-related field
• Have 1-2 years of experience in the pharmaceutical industry or at least 1 year of experience in Pharmacovigilance.
• Previous experience in global drug safety/pharmacovigilance, including both investigational and marketed products, is a plus.

SKILLS AND KNOWLEDGE:

• Ability to effectively handle and prioritize multiple tasks.
• Proficient or fluent in the English language.
• Capable of working efficiently in a team/matrix environment.
• Possess a strong understanding of technical, scientific, and medical information.
• Excellent skills in oral and written communication with a clear professional expression.
• Strong analytical, problem-solving, and decision-making abilities.
• Demonstrates effective interpersonal relationship skills.
• Exhibits initiative and accountability.
• Proficient in time management.
• Attention to detail and a precise, accurate, organized, and structured mindset.
  Additional Information
  AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status

• The MSA is responsible for engaging with both internal and external stakeholders regarding Abbvie products.
• Duties include accurately entering US and international safety information from Clinical Trial sources into the safety database, adhering to Abbvie standard operating procedures and global pharmacovigilance regulations.
• Prioritize case assignments to ensure timely completion in accordance with internal timelines and compliance requirements set by health authorities and licensed partners.
• Meet company standards for quality, compliance, and productivity.
• Stay up to date with conventions, regulations, and skills relevant to case processing.
• Report identified case processing issues to the direct leader.
• Demonstrate Abbvie’s core leadership attributes: Agility and Accountability, Clarity and Courage, Making Possibilities Real, All for One AbbVie, and Smart and Sure Decision Making.
• Perform other duties as assigned according to the needs and work requirements of the organization.
  Qualifications