Pharmacovigilance Coordinator - Buenos Aires, Argentina - PSI CRO
Descripción
Company Description
PSI is a leading Contract Research Organization with more than 25 years of experience in the industry, offering a perfect balance between stability and innovation to both clients and employees.
Job Description:
We are looking for a knowledgeable and proactive Pharmacovigilance Coordinator to join our enthusiastic and vibrant team.
In this role, you will provide day-to-day support to the company's Pharmacovigilance Unit and process safety information throughout the course of a clinical trial.
The scope of responsibilities will include:
- Timely distribution of project-specific Serious Adverse Event (SAE) and Immediately Reportable Adverse Events (IRAE) reports to project teams;
- Data entry into the safety database;
- Nonmedical review of incoming SAE and IRAE reports;
- Maintenance and update of the company's projectspecific SAE distribution lists;
- Review of projectspecific SAE trackers maintained by PSI project teams with focus on their timely update;
- A contact point for Safety Desk and clinical project teams regarding SAE and IRAE reports flow and filing;
- Interaction with IT personnel pertaining to safety line maintenance;
- Maintenance of Pharmacovigilance files, calendars and schedules in an orderly manner.
Qualifications:
- College or University Degree (Biology or Bioscience is preferred);
- Administrative work experience is a plus;
- Experience with safety databases is a plus;
- Full working proficiency in English and Spanish;
- Organizational and planning skills;
- Detailoriented, able to work with multiple tasks in a fastpaced environment;
- Communication and collaboration skills;
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.
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