Veeva RIM - Marlborough

Work closely with business and understand issues. Be proactive. · Maintain and support Veeva RIM and eTMF Projects · ...

The Veeva RIM & eTMF Support Consultant will work closely with business stakeholders to understand regulatory and clinical documentation challenges. · Work closely with business users... · Troubleshoot incidents... · ...

Regulatory Affairs Experience in Regulatory information management VEEVA RIM Demonstrated practical working experience in both processes (eg.xEVMPD) and untilisation of regulatory systems (RIMS,Vault) · ...

The Veeva Vault Support Analyst will work closely with the business and understand the issues. · ...

This job involves working closely with the business and understanding issues to maintain and support Veeva RIM and eTMF Application. · ...

+No C2COur client is looking for an experienced eCTD publishing professional to support the mapping of eCTD metadata from a legacy publishing system into a future-state platform. · Own portions of the data migration and mapping efforts to support Veeva Publishing and eCTD 4.0 ena ...

Our client is seeking an experienced Regulatory Operations Consultant to support Veeva Vault RIM. · ...

No C2COur client is looking for an experienced eCTD publishing professional to support the mapping of eCTD metadata from a legacy publishing system into a future-state platform · ...

+eCTD Publishing Manager, · Regulatory Affairs · We're supporting a U.S.-based biopharmaceutical organization on a highly specialized eCTD Publishing & Veeva Vault RIM initiative. · This role is focused on hands-on eCTD publishing, · data migration into Veeva RIM, · and preparat ...

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year with extensive growth pot ...

Disc Medicine is seeking a detail-oriented and experienced Regulatory Operations senior submission manager. · ...

We are seeking an experienced Regulatory Operations Consultant to support Veeva Vault RIM. · This role will play a key part in submission readiness. · ...

Disc Medicine is seeking a detail-oriented and experienced Regulatory Operations senior submission manager. · ...

Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. · ...

We are seeking a Regulatory Business Analyst with strong Veeva Vault RIM implementation and publishing experience to support regulatory publishing projects and system enhancements. · This is a 6 month contract · ...

We are seeking an IT Validation Specialist to join our team at Net2Source Inc. The successful candidate will be responsible for providing application validation support, documentation, training, and troubleshooting of Veeva systems. · Knowledge of science biology, chemistry, engi ...

We are seeking top talent who share our commitment to patients and have a track record of success in acquiring, developing and commercializing products across the globe. · The Director, Regulatory Operations, will be responsible for day-to-day submission management activities of ...

We are seeking top talent who share our commitment to patients and have a track record of success in acquiring developing and commercializing products across the globe Our colleagues have an opportunity to engage in a fast-paced learning environment and experience individual orga ...

The Associate Director Regulatory Operations will be responsible for submission management across the development pipeline and support the commercial portfolio. · This hands-on position will also assist with regulatory affairs systems applications and tools including supporting s ...

Vor Biopharma is seeking a Senior Director of Information Systems / Digital Systems Lead to help design and deliver the company's digital systems strategy as we prepare for global commercialization of telitacicept. · ...