Global Regulatory Lead
Company Name:
Koch Davis
The proposed person will be responsible for reports to vice president. Close working relationships with research units serve as the global regulatory leader for multiple orphan assets under development as well as potentially other bio-therapeutics research assets. Work with project teams to develop and implement regulatory strategies in support of operating plans for programs including alignment of clinical and commercial targets, preparation of on-time, high-quality, regulatory submissions, understanding the regulatory requirements for key documents including regulatory submissions and registration related documents. Assess and advise teams to mitigate regulatory risks in development projects. Act as the single point of regulatory accountability for the assigned areas of focus for all incoming/outgoing regulatory interactions. Work with teams to develop toxicology, cmc and clinical strategies. Manage regulatory communications among the clinical, clinical operations, regulatory operations and global cmc groups. Collaborate with global regulatory agencies. Oversee preparation, review and editing of sections of regulatory trial documents. Provide answers to regulatory questions for program management, non-clinical and clinical team members, and develop close working relationships with these team members. Integrate knowledge, expertise and negotiation skills to resolve problems, modify procedures, and develop and interpret policy to meet evolving regulatory demands. Maintain working knowledge of relevant global guidance documents and regulations.
Requirements
Not Specified
Education
Not Specified
Client
It is an American multinational pharmaceutical corporation.Estimated Salary: $20 to $28 per hour based on qualifications.
Koch Davis
The proposed person will be responsible for reports to vice president. Close working relationships with research units serve as the global regulatory leader for multiple orphan assets under development as well as potentially other bio-therapeutics research assets. Work with project teams to develop and implement regulatory strategies in support of operating plans for programs including alignment of clinical and commercial targets, preparation of on-time, high-quality, regulatory submissions, understanding the regulatory requirements for key documents including regulatory submissions and registration related documents. Assess and advise teams to mitigate regulatory risks in development projects. Act as the single point of regulatory accountability for the assigned areas of focus for all incoming/outgoing regulatory interactions. Work with teams to develop toxicology, cmc and clinical strategies. Manage regulatory communications among the clinical, clinical operations, regulatory operations and global cmc groups. Collaborate with global regulatory agencies. Oversee preparation, review and editing of sections of regulatory trial documents. Provide answers to regulatory questions for program management, non-clinical and clinical team members, and develop close working relationships with these team members. Integrate knowledge, expertise and negotiation skills to resolve problems, modify procedures, and develop and interpret policy to meet evolving regulatory demands. Maintain working knowledge of relevant global guidance documents and regulations.
Requirements
Not Specified
Education
Not Specified
Client
It is an American multinational pharmaceutical corporation.Estimated Salary: $20 to $28 per hour based on qualifications.
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