7 fsp regulatory affairs consultant jobs found

FSP Regulatory Affairs Consultant - CTR (flexible location UK/EU) United Kingdom, Remote Date posted //2 Job ID R4

FSP Regulatory Affairs Consultant - CTR (flexible location UK/EU) United Kingdom, Remote Date posted //2 Job ID R4

We are currently looking for a Regulatory Affairs Professionals to join one of our clients and act as a (Senior) Regulatory Affairs Consultant CTR. This role can be based in either UK or UE (home/office based) and we have flexibility on levels. In this role you will work closely with other departments to design, implement applications & systems to support regulatory business processes. You will work with key stakeholders to map current processes and organize task forces to define and implement process improvements. You will support the organization by analyzing (as business analyst) and managing and/or coordinating EU CTR process changes and organizational changes. Role responsibilities: Draw models for the business processes (process flows) Moderate workshops with business experts Ensure good communication with stakeholders in the project (verbally and written) Draft new procedures based on new business processes & user requirements...

We are currently looking for a Regulatory Affairs Professionals to join one of our clients and act as a (Senior) Regulatory Affairs Consultant CTR. This role can be based in either UK or UE (home/office based) and we have flexibility on levels. In this role you will work closely with other departments to design, implement applications & systems to support regulatory business processes. You will work with key stakeholders to map current processes and organize task forces to define and implement process improvements. You will support the organization by analyzing (as business analyst) and managing and/or coordinating EU CTR process changes and organizational changes. Role responsibilities: Draw models for the business processes (process flows) Moderate workshops with business experts Ensure good communication with stakeholders in the project (verbally and written) Draft new procedures based on new business processes & user requirements...

We are looking for Regulatory Affairs Professionals CTA/INDon various levels (Consultant, Senior Consultant, Principal Consultant) for a client dedicated project within Parexel FSP Group. The role can be home or office based in various European locations. As the Regulatory Affairs CTA/IND Specialist you will provide technical/coordination support and expertise within the client's vaccines group in particular for the R&D, Global Quality Vaccines & Legal/Patent departments and outside of the group (eg: EMA) to ensure: The appropriate project management related to CTA/IND process with the different stakeholders by issuing the master planning/strategy to ensure timely due submissions and approvals of CTA’s/IND in compliance with ethical and regulatory standards The upload and maintenance of the third country form (related to articles 41 & 46) via the EMA gateway The appropriate project management related to DSUR process with the different...

We are looking for Regulatory Affairs Professionals CTA/INDon various levels (Consultant, Senior Consultant, Principal Consultant) for a client dedicated project within Parexel FSP Group. The role can be home or office based in various European locations. As the Regulatory Affairs CTA/IND Specialist you will provide technical/coordination support and expertise within the client's vaccines group in particular for the R&D, Global Quality Vaccines & Legal/Patent departments and outside of the group (eg: EMA) to ensure: The appropriate project management related to CTA/IND process with the different stakeholders by issuing the master planning/strategy to ensure timely due submissions and approvals of CTA’s/IND in compliance with ethical and regulatory standards The upload and maintenance of the third country form (related to articles 41 & 46) via the EMA gateway The appropriate project management related to DSUR process with the different...

The Role Do you want to be part of something new and up and coming? Do you like digging in deep and solving problems? Do you have a solid understanding of eCTDs and the nuances of successfully getting a submission to the Health Authorities? Come help us shape a new paradigm for submissions publishing. Veeva’s Vault RIM suite is the industry’s only unified software solution that provides fully integrated regulatory information management (RIM) capabilities including data and document management, submission publishing, and archival on a single cloud-based platform. Veeva Systems is looking for experts in Regulatory Operations, specifically, eCTD publishing, who are dedicated and passionate about helping our customers hit their submission deadlines. As a key member of the Professional Services team, the Publishing Consultant will be responsible for understanding our customers' global regulatory eCTD publishing needs and assisting their use of Vault Submissions Publishing....