Director, Regulatory job opportunity at Precision Medicine Group.



bot
Precision Medicine Group Director, Regulatory
Experience: 10-years
Pattern: full-time
apply Apply Now
Salary:
Status:

Directing

Copy Link Report
degreeBachelor's (B.Sc.)
Singapore

Provide strategic, technical, and regulatory guidance to #clients and team members in the area of clinical development of #human #medicinal products and drug development life cycle Establish operational objectives and assignments for assigned team members Track and report regulatory function metrics and key performance indicators Oversee, review and provide strategic input on applications to Regulatory Authorities including, but not limited to, #CTA/IND, annual reports, routine amendments, scientific advice/regulatory authority meetings, orphan designations, paediatric planning, and expedited pathways As needed, review documents intended for submission to the Regulatory Authorities and/or Ethics Committees to ensure compliance with regulatory standards Select, train, develop, coach and manage the performance of Regulatory Managers, ensuring the sharing of best practices across the team Oversee resource allocation and utilization of Regulatory Managers. __ As needed, represent Global #Regulatory Affairs at project team meetings with both external and internal customers and manage/oversee regulatory workflow between departments Provide oversight to filing and study teams regarding regulations/guidelines and company #SOPs to ensure successful and high-quality regulatory applications Ensure budgets and plans meet corporate requirements Provide ICH/GCP/Regulation guidance, advice and training to internal and external clients Participate in developing, implementing, and maintaining the corporate quality initiatives across business units within Clinical Solutions/Precision for Medicine Implement regulatory tools to support the department Assist in developing, modifying and executing company policies that affect Regulatory Affairs and may impact other departments Support QA audits and/or assign applicable team members to participate in audits Establishes and maintains a high level of technical knowledge in the area of product development and international regulatory affairs. Interprets emerging regulatory requirements and collaborates in impact assessment and implementation Supports Business Development in generation of customer focused, well-presented regulatory proposal content and budgets, partnering with other functional areas as required to define bid content, strategy, scope of work

Other Ai Matches

Regulatory Manager / Senior Regulatory Manager (Clinical Trials) Applicants are expected to have a solid experience in handling Managing related tasks
Associate Medical Director - Market Access Marketing - Applicants are expected to have a solid experience in handling Medical related tasks
Principal Financial Analyst Applicants are expected to have a solid experience in handling Analyst related tasks
Non-Registered Histotechnician Applicants are expected to have a solid experience in handling Technician related tasks
Director, Regulatory Applicants are expected to have a solid experience in handling Directing related tasks
Medical Writing Intern, Medical Communications Applicants are expected to have a solid experience in handling Medical related tasks
IT Senior Support Specialist (SAP SuccessFactors) Applicants are expected to have a solid experience in handling Specialist related tasks
Clinical Research Associate II/ Senior Clinical Research Associate - Clinical Trial Services Applicants are expected to have a solid experience in handling Clinical assistant related tasks
Feasibility Associate/ Senior Feasibility Associate Applicants are expected to have a solid experience in handling Associate related tasks
Principal Financial Analyst* Applicants are expected to have a solid experience in handling Analyst related tasks
Feasibility Associate/ Senior Feasibility Associate Applicants are expected to have a solid experience in handling Associate related tasks
Associate Director, Primary Data Collection Applicants are expected to have a solid experience in handling Associate related tasks
Regulatory and Start Up Specialist Applicants are expected to have a solid experience in handling Specialist related tasks
Join our Talent Community- Clinical Trial Manager Applicants are expected to have a solid experience in handling Management related tasks
Senior Clinical Project Manager Applicants are expected to have a solid experience in handling project management related tasks
Feasibility Associate/ Senior Feasibility Associate Applicants are expected to have a solid experience in handling Associate related tasks
Clinical Research Associate II/Senior Clinical Research Associate Applicants are expected to have a solid experience in handling Research Associate related tasks
Regulatory and Start Up Specialist/ Senior Regulatory and Start Up Specialist Applicants are expected to have a solid experience in handling Specialist related tasks
Senior Data Analyst Applicants are expected to have a solid experience in handling Analytics related tasks
Content Developer Applicants are expected to have a solid experience in handling Developer related tasks
Director, Regulatory* Applicants are expected to have a solid experience in handling Director related tasks
Consultant, Market Access Applicants are expected to have a solid experience in handling Consultant related tasks
IT Senior Support Specialist (SAP SuccessFactors)* Applicants are expected to have a solid experience in handling Specialist related tasks