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Pharmacovigilance Associate

0-5 years
Not Disclosed
10 Aug. 12, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

About the Role

Please note: This vacancy has expired. However, you can explore similar roles below.

At ICON, our people are what set us apart. Our diverse team empowers us to be a better partner for our customers and helps us fulfill our mission to advance and improve patients' lives.

Our "Own It" culture is driven by four core values ​​that unite us as individuals and distinguish us as an organization: accountability, collaboration, partnership, and integrity. We aim to be the leading contract drug development organization that consistently delivers excellence to our clients and patients. That's our vision, and we are actively pursuing it. We need talented individuals who share this vision.

If you're as motivated as we are, we hope you'll join us. You'll work in a dynamic, supportive environment with some of the brightest and kindest people in the industry, helping shape its future.

We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team. As a Pharmacovigilance Associate at ICON, you will play a crucial role in ensuring drug safety and efficacy, monitoring adverse events, and contributing to the overall quality and compliance of pharmacovigilance activities.

Job Details:

  • Collect, process, and evaluate adverse event reports from various sources, including healthcare professionals, clinical trial sites, and regulatory authorities.
  • Perform case processing activities such as data entry, medical coding, and signal detection in accordance with established procedures and regulatory requirements.
  • Assist in preparing periodic safety reports, risk management plans, and other pharmacovigilance documentation.
  • Collaborate with cross-functional teams in clinical operations, regulatory matters, medical writing, and more to ensure timely and accurate reporting of safety information.
  • Participate in the continuous improvement of pharmacovigilance processes, systems, and standard operating procedures.

Desired Profile:

  • Bachelor's degree in life sciences, pharmacy, nursing, or a related field.
  • Experience in pharmacovigilance or drug safety activities within the pharmaceutical or contract research organization (CRO) industry.
  • In-depth knowledge of relevant regulations, guidelines, and industry best practices in pharmacovigilance and drug safety.
  • Familiarity with adverse event reporting databases and safety management systems.
  • Excellent attention to detail with the ability to accurately interpret and record safety information.
  • Strong written and verbal communication skills, with the ability to work effectively with cross-functional teams.

Benefits of Working at ICON:

Our success depends on the quality of our people. That’s why we prioritize cultivating a culture that rewards performance and develops talent.

We offer a competitive salary package, regularly benchmarked against competitors to stay attractive. Our annual bonuses reflect the achievement of performance targets, benefiting both you and the company.

We also provide a variety of health-related benefits for our employees and their families, along with competitive retirement plans and related benefits like life insurance. This allows you to save and plan with confidence over the long term.

But beyond competitive pay and comprehensive benefits, you'll benefit from an environment that fulfills your sense of purpose and drives lasting change.

ICON is an equal opportunity and inclusive employer committed to providing a workplace free from discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Please let us know if you require reasonable adjustments to any part of the application process or to perform the essential functions of the position due to a medical condition or disability.

If you’re interested in the role but unsure if you meet all the requirements, we encourage you to apply anyway. At ICON, we might have the perfect opportunity for you, whether in this role or another one.