Pharmacovigilance Associate

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0-5 years

Not Disclosed

Tokyo

10 Aug. 5, 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, 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

Join Our Team at ICON: Pharmacovigilance Associate

About Us:

At ICON, our people set us apart. Our diverse team empowers us to be better customer partners and fulfill our mission to advance and improve the lives of patients. Our "Own It" culture is driven by four core values that unite us: accountability and delivery, collaboration, partnership, and integrity. We aim to be a leading contract drug development organization that delivers excellence to our clients and patients at every touchpoint.

Our Vision:

We are committed to being chosen as a partner in drug development. We act on this vision and seek talented individuals to share it. If you're motivated and passionate, we hope you'll join us. You'll work in a dynamic, supportive environment with some of the brightest and kindest people in the sector, helping shape the industry.

Position: Pharmacovigilance Associate

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

Job Responsibilities:

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 the preparation of periodic safety reports, risk management plans, and other pharmacovigilance documents.
Collaborate with cross-functional teams in clinical operations, regulatory matters, medical writing, etc., to ensure timely and accurate reporting of safety information.
Participate in 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 in 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. We prioritize cultivating a culture that rewards performance and develops talent.

Competitive salary package, regularly benchmarked against competitors.
Annual bonuses reflecting performance targets achieved by both the company and you.
Comprehensive health-related benefits for employees and their families.
Competitive retirement plans and related benefits, including life insurance.
An environment that fulfills your sense of purpose and drives lasting change.

Equal Opportunity Employer:

ICON is committed to providing a workplace free of 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.

Reasonable Adjustments:

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

Apply Today:

Even if you’re not sure you meet all the requirements, we encourage you to apply. ICON may have everything you are looking for, whether in this role or another.

Join us and be part of something meaningful!

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Pharmacovigilance Associate

Job Description

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