Senior Pharmacovigilance Associate
hace 4 semanas
At ICON, we're driven by a shared vision to advance and improve patients' lives. Our diverse teams enable us to become a better partner to our customers, and we're committed to delivering excellence in every touch-point.
We're seeking a highly skilled Pharmacovigilance Associate to join our team. As a key member of our Pharmacovigilance team, you'll be responsible for responding to medical information inquiries from healthcare professionals, consumers, regulators, and internal colleagues.
Key responsibilities include:
- Triage information received based on regulatory requirements and applicable SOPs to ensure adverse events, product complaints, and medical information queries are handled in a compliant manner.
- Complete adverse event follow-up by phone or in writing based on requirements for each client and/or case.
- Prioritize and complete multiple projects within established time frames.
- Manage client projects, including managing client relationships and project budgets.
- Enter information for medical information inquiries into medical information databases, tracking systems, and project-specific forms to ensure accurate data entry.
- Maintain a library of responses to Frequently Asked Questions and Standard Response Letters.
- Prepare Standard Response letters, including conducting literature searches and article summaries.
- Respond to medical information inquiries within pre-determined timelines and constraints, requesting assistance from clients and safety physicians as appropriate.
- Identify individual Case Safety Reports and technical product complaints and forward them to relevant stakeholders within pre-determined timelines.
- Assist with or perform reconciliation of safety databases, safety tracking systems, medical information databases, product complaint database, and clinical databases.
- Monitor and interpret worldwide regulations pertaining to medical information and pharmacovigilance, providing regulatory expertise to colleagues and clients.
- Assist with regulatory agency inspections, client audits, and internal audits.
- Participate as an active member of multidisciplinary teams to successfully achieve project and corporate goals.
Requirements include:
- Strong written and oral communication skills in English.
- Bachelor's degree completed (Doctor or Nursing).
- At least 1 year of experience with customer service experience similar to a call center.
We offer a competitive salary package, annual bonuses, and a range of health-related benefits to employees and their families. We're an equal opportunity and inclusive employer, committed to providing a workplace free of discrimination and harassment.
-
Senior Pharmacovigilance Manager
hace 4 semanas
Xico, México Icon A tiempo completoAt ICON plc, a world-leading healthcare intelligence and clinical research organization, we are seeking a highly skilled and experienced Senior Pharmacovigilance Manager to join our team.The successful candidate will be responsible for managing personnel within Pharmacovigilance and providing expertise in tasks such as Serious Adverse Events (SAE)...
-
Senior Pharmacovigilance Associate
hace 4 semanas
Xico, México Icon A tiempo completoAt ICON, we're driven by a shared vision to advance and improve patients' lives. Our diverse teams enable us to become a better partner to our customers, and we're committed to delivering excellence in every aspect of our work.As a Senior Pharmacovigilance Associate, you'll play a critical role in ensuring the safety of our clients' products. Your...
-
Pharmacovigilance Associate
hace 1 mes
Xico, México Icon Plc A tiempo completoJob Title: Pharmacovigilance Associate - Regulatory ExpertAt ICON plc, we are seeking a highly skilled Pharmacovigilance Associate to join our team. As a key member of our pharmacovigilance team, you will be responsible for reviewing and processing safety events, generating data listings, and providing input on safety tracking systems.Key...
-
Pharmacovigilance Manager
hace 4 semanas
Xico, México Icon Plc A tiempo completoJob Summary:We are seeking a highly skilled Pharmacovigilance Manager to join our team at ICON plc. As a key member of our Pharmacovigilance department, you will be responsible for managing personnel and providing expertise in various areas, including Serious Adverse Events (SAE) management, periodic safety reports, and regulatory compliance.Key...
-
Senior Pharmacovigilance Associate
hace 3 días
Xico, México Icon A tiempo completoJob Title:Senior Pharmacovigilance Associate - Global Regulatory ExpertAbout ICON:At ICON, we're driven by a shared mission to advance and improve patients' lives. Our diverse teams enable us to become a better partner to our customers, and we strive for excellence in every touch-point.Role Overview:We're seeking an experienced Senior Pharmacovigilance...
-
Pharmacovigilance Specialist
hace 1 mes
Xico, México Engineeringuk A tiempo completoPharmacovigilance Associate Job DescriptionAt Engineeringuk, we're seeking a highly skilled Pharmacovigilance Associate to join our team. As a key member of our pharmacovigilance team, you will play a crucial role in ensuring the safety of our clients' products.Responsibilities:Review and process safety events, including pre-marketing, post-marketing,...
-
Pharmacovigilance Specialist
hace 4 semanas
Xico, México Icon A tiempo completoJob Summary: We are seeking a skilled Pharmacovigilance Associate to join our team at ICON plc. As a Pharmacovigilance Associate, you will play a crucial role in ensuring the safety of our clients' products by reviewing and processing safety events, generating data listings, and performing adverse event follow-up.Key Responsibilities:Review and process...
-
Senior Pharmacovigilance Specialist
hace 1 semana
Xico, México Thermo Fisher Scientific A tiempo completoAbout the RoleAs a Senior Pharmacovigilance Specialist at Thermo Fisher Scientific, you will play a critical role in ensuring the safety of new drugs in clinical trials and marketed products across all major markets. Your expertise in pharmacovigilance requirements will be essential in managing the safety profile of these products.Key...
-
Pharmacovigilance Associate
hace 4 semanas
Xico, México Icon A tiempo completoJob Summary: We are seeking a highly skilled Pharmacovigilance Associate to join our team at ICON. As a key member of our clinical research organization, you will play a critical role in ensuring the safety of our clients' products.Key Responsibilities:Receive and process individual case safety reports (ICSRs) from clinical trials, spontaneous reports, and...
-
Pharmacovigilance Expert
hace 2 días
Xico, México Icon Plc A tiempo completoAt Icon Plc, we're driven by a shared purpose: advancing and improving patients' lives through clinical research excellence. We foster a collaborative environment where talented individuals can thrive and make a meaningful impact.We're seeking a skilled Pharmacovigilance Associate to join our dynamic team. As a key member, you'll play a critical role in...
-
Supervisor, Pharmacovigilance Specialist
hace 4 semanas
Xico, México Icon Plc A tiempo completoAt ICON plc, we are committed to advancing clinical research and providing high-quality services to our clients. As a Supervisor, Pharmacovigilance, you will play a critical role in supporting the creation and updates of SOPs, participating in departmental process and system improvement initiatives, and supervising a subordinated group.Key...
-
Global Drug Safety Associate
hace 2 semanas
Xico, México Novo Nordisk A tiempo completoAs a Drug Safety Associate at Novo Nordisk, you will be responsible for performing initial evaluations, case entry, and verification of reported adverse events in the Argus safety database. This involves ensuring accurate coding of events using MedDRA and evaluating causality, seriousness, and listedness for all cases. You will also assess the need for...
-
Senior Associate, Adaptation
hace 3 semanas
Xico, México Global Green Growth Institute A tiempo completoJob Summary:The Global Green Growth Institute (GGGI) is seeking a highly skilled and experienced professional to fill the position of Senior Associate, Adaptation. This role will play a key part in supporting the implementation of GGGI Mexico's program in integrated planning for climate resilient green growth.About the Role:As a Senior Associate,...
-
Drug Safety Associate
hace 4 semanas
Xico, México Novo Nordisk A tiempo completoJob SummaryWe are seeking a highly skilled Drug Safety Associate to join our team at Novo Nordisk in Mexico City. As a key member of our Global Business Service Centre, you will play a critical role in ensuring the quality and integrity of our safety data.Key ResponsibilitiesPerform initial evaluation, case entry, and verification of reported adverse events...
-
Senior Financial Associate
hace 4 semanas
Xico, México Celanese International Corporation A tiempo completoJob SummaryAs a Senior Financial Associate at Celanese International Corporation, you will play a key role in supporting the Americas Cash Accounting team. This position requires strong analytical and problem-solving skills, as well as excellent communication and teamwork abilities.Key Responsibilities:Perform cash-related journal entries, financial...
-
Senior Finance Associate
hace 1 mes
Xico, México Fusemachines A tiempo completoAbout the RoleFusemachines, a pioneering AI company, is seeking a highly skilled Senior Finance Associate to join its finance department. As a key member of the team, you will play a pivotal role in ensuring the financial health and strategic goals of the organization.Key ResponsibilitiesFinancial Reporting and Analysis: Prepare, analyze, and interpret...
-
Financial Associate
hace 3 semanas
Xico, México Bbvacib A tiempo completoAs a Financial Associate at Bbvacib, you will be responsible for preparing proposals, presentations, and pitches to current and prospective clients.Additionally, you will assist other members of the team in identifying and exploring potential new business by analyzing client's financial profile and market/industry variables.You will synthesize research...
-
Senior Safety Data Specialist
hace 4 días
Xico, México Novasyte A tiempo completoJob OverviewAs a Senior Safety Data Specialist, you will play a key role in reviewing, assessing, and processing safety data and information across various service lines. This involves receiving data from multiple sources, analyzing it, and distributing reports to both internal and external stakeholders while adhering to applicable regulations and...
-
Cyber Risk Senior Associate
hace 1 mes
Xico, México Kroll A tiempo completoJob Title: Senior Associate, Cyber RiskIn today's complex business landscape, our professionals at Kroll bring clarity to our clients' most pressing governance, risk, and transparency challenges. We foster a culture of diversity and inclusion, where our team members can thrive and grow.Key Responsibilities:Deliver strong technical skills in support of cyber...
-
Safety Program Manager, Global Projects
hace 1 semana
Xico, México Thermo Fisher Scientific A tiempo completoThermo Fisher Scientific seeks an experienced Safety Program Manager to oversee global projects and ensure compliance with regulatory requirements. This role requires a strong understanding of pharmacovigilance procedures and the ability to manage multiple aspects of projects, including contractual, procedural, and regulatory requirements.Key...