pharmacovigilance

Use Your Power for PurposeThe Safety Intern will provide administrative and operational support to the Safety team by assisting with case processing activities, document management, and data entry tasks. This internship offers hands-on experience in pharmacovigilance and safety operations, supporting compliance with regulatory requirements and company...

Job Description The Associate Director, Study Data Services (M-track) leads and develops a programming and reporting team - set goals, assign work, coach performance, and manage recruiting/onboarding - while communicating status and risks to leadership and partners. Provide hands-on technical review, solutioning support, enforce SOPs/standards, manage...

Job Description The Associate Director, Study Data Services (M-track) leads and develops a programming and reporting team - set goals, assign work, coach performance, and manage recruiting/onboarding - while communicating status and risks to leadership and partners. Provide hands-on technical review, solutioning support, enforce SOPs/standards, manage...

Position Purpose The Cluster Medical Lead will be responsible for the delivery of the medical strategy plan and execution of scientific activities in the cluster. The Cluster Medical Lead will have overall responsibility for ensuring high quality scientific medical input and clinical strategic direction to support the Therapeutic Area teams to deliver...

Job DescriptionAs the Associate Director, Clinical Data Management (CDM) Geography Lead, you will play a key leadership role in shaping data management operations and talent across your assigned geography. You will drive operational excellence, quality, compliance, and resource optimization while partnering with leaders across the organization to advance...

Job Description As the Associate Director, Clinical Data Management (CDM) Geography Lead, you will play a key leadership role in shaping data management operations and talent across your assigned geography. You will drive operational excellence, quality, compliance, and resource optimization while partnering with leaders across the organization to advance...

Job Description As the Associate Director, Clinical Data Management (CDM) Geography Lead, you will play a key leadership role in shaping data management operations and talent across your assigned geography. You will drive operational excellence, quality, compliance, and resource optimization while partnering with leaders across the organization to advance...

Job DescriptionThe Specialist, International Labeling Support will partner cross functionally within GRACS and cross divisionally where applicable to ensure all the Labeling and Artworks regulatory operational activities in scope of ILS are planned, managed, and executed timely, accurately and in a compliant way. The role includes any identification of...

Ayúdanos a adelantarnos a las enfermedades junto con nuestra Área de Farmacovigilancia.Formación requerida: Estudiante avanzado de Farmacia, Medicina, Enfermería, Salud Pública u otra área relacionada. Mínimo a un año para terminar.Otros requisitos: Debe estar matriculado/a en una universidad de Costa Rica durante la pasantía.Requisitos de idioma:...

Job Description These roles are responsible for handling inbound and outbound interactions (phone, email and other channels) from patients, HCPs and customers, while accurately identifying, documenting and routing product quality complaints and related safety information.This role ensures excellent customer experience, compliant intake of information, and...

Company DescriptionAbout AbbVieAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and...

Job DescriptionThe Regional Dossier Publisher (RDP) will work within the Company's Global Regulatory Affairs and Clinical Safety (GRACS) organization, in the Regional Regulatory Operations Department (RRO) supporting regional publishing activities for the LATAM region while also contributing to cross-regional publishing activities as needed.  The RDP is...

Company DescriptionAbout AbbVieAbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and...

Job DescriptionThe Specialist of Regulatory Planning & Publishing works closely with various stakeholders of regulatory and safety submissions to assist in planning, execution, and management of activities that deliver high quality and timely regulatory submissions. Additionally, the incumbent may be involved in supporting internal or external process...

Job DescriptionThe Regulatory Submissions Planner supports the preparation of regulatory submissions and manages registration tracking from a regulatory operations perspective ensuring alignment with strategic target dates across the region.As part of a cross-functional team and assigned programs, he/she/they will manage all operational activities for...

Remote Clinical Trial Support Specialist (Multiple Openings) Company: Angel City VA — Virtual Clinical Research Support. Location: Remote (Philippines, Latin America, Georgia, Ukraine, Moldova, Armenia, Azerbajan. Employment Type: Full-Time, Part-Time, and Project-Based Opportunities Available Join Angel City VA — Where Top Clinical Research Talent Gets...

OBJECTIVEConduct activities and interactions consistent with Company values and in compliance with the Code of Conduct and supporting Policies and Standards relevant to Patient Safety. Complete all required training on the AZ Code of Conduct and supporting Policies and Standards on time. Report potential issues of noncompliance.Ensure and monitor compliance...