Pharmacovigilance Reporting Associate (Intelligence) at ICON Plc | Apply Now
A Pharmacovigilance Reporting Associate opportunity is available at ICON plc in Mexico City for professionals interested in safety reporting for clinical trials and post-marketing activities. Interested candidates are encouraged to apply soon.
- Position: Pharmacovigilance Reporting Associate
- Location: Mexico City, Mexico
- Job Reference: JR154023
- Department: Drug Safety
About ICON plc
ICON plc is a world-leading healthcare intelligence and clinical research organization. The company is committed to fostering an inclusive environment that drives innovation and excellence in clinical development. With a focus on improving patient outcomes, ICON operates globally, providing a range of services to the pharmaceutical, biotechnology, and medical device industries.
Pharmacovigilance Reporting Associate Job Description
As a Pharmacovigilance Reporting Associate at ICON, the individual will be responsible for the accurate and timely preparation of safety reports related to clinical trials and post-marketing activities. This role requires a strong commitment to quality and compliance with regulatory requirements.
Eligibility Criteria
- Bachelor’s degree in life sciences, or a related field.
- Experience in pharmacovigilance or drug safety, with an understanding of safety reporting processes and regulatory requirements preferred.
- Excellent attention to detail and organizational skills, with the ability to prepare and review complex safety reports accurately.
- Strong communication and collaboration skills, with experience working effectively within a multidisciplinary team.
- Ability to manage multiple tasks and prioritize effectively in a fast-paced, regulated environment.
Pharmacovigilance Reporting Associate – Key Responsibilities
- Serve as safety reporting intelligence processor and/or lead for multiple safety reporting or safety reporting intelligence stand-alone projects, providing management support as designated.
- Recognize, exemplify, and adhere to ICON’s values, which center around commitment to People, Clients, and Performance.
- Embrace and contribute to a culture of process improvement with a focus on streamlining processes and adding value to the business.
- Complete all departmental project activities accurately in accordance with ICON SOPs, Study Specific Procedures, regulatory requirements, and client processes.
- Responsible for safety reporting or safety reporting intelligence activities on assigned projects, working in a customer-focused approach and an audit and inspection-ready mindset.
- Demonstrate skills pertaining to client management, safety reporting, project scope, submission compliance, quality, and budget.
What ICON can offer you
ICON prioritizes building a diverse culture that rewards high performance and nurtures talent. In addition to a competitive salary, ICON offers a range of additional benefits designed to support well-being and work-life balance for employees and their families. Examples of benefits include various annual leave entitlements, health insurance options, competitive retirement planning, and a global employee assistance program.
This is an excellent opportunity for qualified candidates to join ICON plc as a Pharmacovigilance Reporting Associate. Interested individuals are encouraged to apply before the deadline to take the next step in their career in the pharmaceutical industry.
