Safety submissions specialist - Bangalore, Karnataka, India

As a Submission Specialist, Promotional Content, you will play a crucial role in ensuring the timely and accurate submission of healthcare marketing materials to regulatory authorities. · ...

Position Summary · The Safety Submission Specialist, under minimal supervision, will assume the responsibility of reviewing and transmission of required individual cases safety reports (ICSRs) for submission (paper and electronic) to global regulatory agencies, business partners, ...

· Position Summary: · The Safety Submission Specialist, under minimal supervision, will assume the responsibility of reviewing and transmission of required individual cases safety reports (ICSRs) for submission (paper and electronic) to global regulatory agencies, business partn ...

We are seeking a detail-oriented professional to manage promotional pharmaceutical communication deliverables and ensure compliance with Medical, · Legal,and Regulatory (MLR) standards. · Review documents for compliance with MLRgridandstandards,,, ...

Position Summary: · The Safety Submission Specialist, under minimal supervision, will assume the responsibility of reviewing and transmission of required individual cases safety reports (ICSRs) for submission (paper and electronic) to global regulatory agencies, business partners ...

Deliver end-to-end submissions to agreed timelines and in compliance with Regulatory Authority regulations and guidelines. · ...

This role offers an excellent opportunity to develop your expertise in Regulatory Affairs while collaborating with cross-functional teams and gaining exposure to global submission processes. · ...

This role offers an excellent opportunity to develop your expertise in Regulatory Affairs while collaborating with cross-functional teams and gaining exposure to global submission processes. · ...

Regulatory Specialist works closely with global submission teams to deliver end-to-end submissions within agreed timelines and in compliance with Regulatory Authority regulations. · ...

This role offers an excellent opportunity to develop your expertise in Regulatory Affairs while collaborating with cross-functional teams and gaining exposure to global submission processes. · ...

This role offers an excellent opportunity to develop your expertise in Regulatory Affairs while collaborating with cross-functional teams and gaining exposure to global submission processes. · ...

This role offers an excellent opportunity to develop your expertise in Regulatory Affairs while collaborating with cross-functional teams and gaining exposure to global submission processes.We are looking for professionals with these required skills to achieve our goals: · Degree ...

VCLS busca a un experto Senior Publishing Specialist con experiencia para trabajar en nuestro equipo durante las horas nocturnas (6pm-0230am). Esta persona será crucial para asegurar la entrega puntual y precisa de documentos regulatorios a autoridades mundiales. · ...

VCLS busca un especialista senior en publicaciones para su equipo nocturno. · ...

+Senior Publishing Specialist to join our team on the night shift 6pm-0230am. Ensuring timely and accurate submission of regulatory documents to health authorities worldwide. · + · + · Lead eCTD publishing process for clinical and regulatory submissions. · Perform quality control ...

The Regulatory Affairs senior specialist will be responsible for planning, preparing, and managing regulatory submissions and compliance activities for medical devices under CDSCO (India), EU MDR, and US FDA frameworks. · ...

The Regulatory Affairs senior specialist will be responsible for planning, preparing and managing regulatory submissions and compliance activities for medical devices under CDSCO (India). · ...

You will be responsible for managing and overseeing end-to-end content submission processes while ensuring submissions are timely, accurate, and compliant with given Brand/AMA guidelines. · ...

This role supports regulatory management by ensuring alignment between GSK's business objectives, strategy, · and the necessary processes to meet Health Authority requirements for regulatory submissions.This role will provide YOU the opportunity to lead key activities to progress ...

We are looking for an experienced Technical Support Specialist with strong expertise in pharmacovigilance (PV) systems. · Experience: 4-8 years in PV systems technical support and configuration. · Technical Expertise: Argus Safety, Axway Gateway, Apex, BI Publisher. · ...