Regulatory Affairs Consultants (San Francisco)
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We are looking for aRegulatory Affairs Consultant to support several ongoing projects at about 10-20 hours per week. This role is remote.
Job Duties
• Work closely with Pharmatech and our clients executive leadership team to lead the development of regulatory strategies and objectives that result in the successful registration and post-approval commercialization of the clients product.
• Develop, lead, and drive the execution of the regulatory strategy from pre-IND to launch, commercialization and product lifecycle management
• Plan and oversee activities in support of all regulatory submissions
• Serve as the primary company contact with the US FDA to achieve company regulatory objectives, by fostering strong relationships and acting as a credible, reputable, and effective advocate for company
• Provide regulatory guidance to the Client across all areas of regulatory affairs throughout all stages from product development
• Experience working with government agencies sponsoring drugs and biologics is highly desirable. Combination Drug and Device regulatory submission experience is a plus.
• Participate as part of internal regulatory team to define and execute the regulatory strategy
• Support the preparation of briefing packages, and regulatory submission documents as needed , providing insightand expertise
Education and Qualifications
• Advanced degree from accredited college or university in science, biomedical engineering, plus a m inimum of 10 years of experience in Filing Global Regulatory Applications for the following registrations NDAs, ANDAs, INDs and BLAs for pharmaceutical and Biotech products.
• Proven record in submission of licenses and authorizations for the maintenance of existing products; International registrations and dossiers and execution of regulatory strategies that align with business deliverables
• Provide Regulatory Affairs support during internal and external audits
• Plans schedules for regulatory deliverables on a project and monitors project through completion
• Responsible for communicating business-related issues or opportunities to next management level
Pharmatech Associates, Inc. providesequal employment opportunityto all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law.
Contact Us
Our unique approach can help your company navigate the complexities of launching a drug, biologic or medical device into multiple markets. The first step? Connecting. Simply fill out our form and a representative will follow-up shortly.
1.877.787.0177
510.732.0177
#J-18808-Ljbffr
Apply Now
Apply Now
We are looking for aRegulatory Affairs Consultant to support several ongoing projects at about 10-20 hours per week. This role is remote.
Job Duties
• Work closely with Pharmatech and our clients executive leadership team to lead the development of regulatory strategies and objectives that result in the successful registration and post-approval commercialization of the clients product.
• Develop, lead, and drive the execution of the regulatory strategy from pre-IND to launch, commercialization and product lifecycle management
• Plan and oversee activities in support of all regulatory submissions
• Serve as the primary company contact with the US FDA to achieve company regulatory objectives, by fostering strong relationships and acting as a credible, reputable, and effective advocate for company
• Provide regulatory guidance to the Client across all areas of regulatory affairs throughout all stages from product development
• Experience working with government agencies sponsoring drugs and biologics is highly desirable. Combination Drug and Device regulatory submission experience is a plus.
• Participate as part of internal regulatory team to define and execute the regulatory strategy
• Support the preparation of briefing packages, and regulatory submission documents as needed , providing insightand expertise
Education and Qualifications
• Advanced degree from accredited college or university in science, biomedical engineering, plus a m inimum of 10 years of experience in Filing Global Regulatory Applications for the following registrations NDAs, ANDAs, INDs and BLAs for pharmaceutical and Biotech products.
• Proven record in submission of licenses and authorizations for the maintenance of existing products; International registrations and dossiers and execution of regulatory strategies that align with business deliverables
• Provide Regulatory Affairs support during internal and external audits
• Plans schedules for regulatory deliverables on a project and monitors project through completion
• Responsible for communicating business-related issues or opportunities to next management level
Pharmatech Associates, Inc. providesequal employment opportunityto all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law.
Contact Us
Our unique approach can help your company navigate the complexities of launching a drug, biologic or medical device into multiple markets. The first step? Connecting. Simply fill out our form and a representative will follow-up shortly.
1.877.787.0177
510.732.0177
#J-18808-Ljbffr
Apply Now
Apply Now