Entry Level Pharmacovigilance Professional - Bengaluru

We are looking for a highly skilled and experienced Pharmacovigilance professional with expertise in Japanese (N3 N1) to join our team. The ideal candidate will have a strong background in the Pharmaceutical and Life Sciences industry. · Roles and Responsibility · Conduct thoroug ...

As an Integration Engineer, you will provide consultative Business and System Integration services to assist clients in implementing effective solutions. Your typical day will involve understanding and translating customer needs into actionable business and technology solutions, ...

We're seeking a Pharmacovigilance Reporting Specialist to join our team. You will prepare pharmacovigilance reports ensuring compliance with regulatory requirements. · ...

Graduate Pharmacovigilance AssociateICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinic ...

Quanticate is seeking an experienced Senior Pharmacovigilance Scientist to take ownership of pharmacovigilance delivery across clinical development and post-marketing programmes. · ...

Quanticate is seeking an experienced Senior Pharmacovigilance Scientist to take ownership of pharmacovigilance delivery across clinical development and post-marketing programmes. · ...

As a Safety Pharmacovigilance Staff member, you will provide essential administrative support and ensure the maintenance and accuracy of the systems used by the team. Your responsibilities will include: · Providing administrative support to the team as required. · Maintaining inf ...

This role offers visible impact,strong learning opportunities,and the chance to grow within a global safety organisation.Lead key activities to progress YOUR career. · Expert in monitoring compliance by GSK and Third Parties with PVASC. · Monitoring compliance with regulatory and ...

As a Medical Writer at Parexel, your role involves utilizing your strong scientific knowledge, writing skills, and patient focus to effectively communicate complex scientific data to various stakeholders, including regulatory agencies, medical professionals, and the general publi ...

You will support the literature monitoring and review activities that help keep our safety and medical teams informed. You will work with colleagues across pharmacovigilance, medical affairs, and regulatory teams. · ...

++Assists in performing safety monitoring activities in cooperation with project Medical Monitor/Medical Officer and other relevant project team members+ · Reviews safety events+ · +Assists in the collection, assessment, monitoring, review and reporting of adverse drug reaction c ...

Perform Safety literature assessment activities for signal detection and aggregate reports purposes in accordance with their procedures and regulatory requirements. · ...

As a Risk and Compliance Representative, you will support service delivery through quality and risk management. You will increase awareness of compliance policies and processes, ensure adherence to compliance standards, conduct risk assessments, and provide guidance on compliance ...

We are seeking an experienced Senior Pharmacovigilance Scientist to lead safety operations on complex projects and provide expert pharmacovigilance guidance throughout study set-up and delivery. · ...

Quanticate is seeking an experienced Senior Pharmacovigilance Scientist to take ownership of pharmacovigilance delivery across clinical development and post-marketing programmes. · This is a hands-on, client-facing role with responsibility for leading safety operations on complex ...

We are seeking an experienced Manager with strong consulting skills and deep industry expertise in Regulatory Affairs and Pharmacovigilance to lead IT implementation projects in regulated GxP environments. · Lead regulatory strategy/ pharmacovigilance (Safety) strategy developmen ...

Hiring Pharmacovigilance Professionals (CL8 & CL9) for Medical Reviewer / Signal Management roles in Chennai and Bangalore. · Medical Reviewer: MBBS / MD · Signal Management: Life Science Graduate · ...

Job Overview · The objective of this position is to provide medical expertise in the evaluation of safety data from a variety of sources as part of the overall pharmacovigilance process and determine the medical and scientific relevance of serious adverse event reports within the ...

We're seeking an experienced Manager – Regulatory Compliance to lead IT implementation projects in regulated GxP environments. · 8–12 years of hands-on experience in regulatory area · Proven experience in regulatory affairs, pharmacovigilance and RIMS implementation or management ...

We are seeking an experienced Senior Manager with strong consulting skills and deep industry expertise in Regulatory Affairs and Pharmacovigilance to lead IT implementation projects in regulated GxP environments. · The opportunity · We are seeking an experienced Senior Manager wi ...