Pharmatech Associates
Regulatory Affairs Consultant, Orphan Drug
Pharmatech Associates, Boston, Massachusetts, us, 02298
Pharmatech is proud to be an equal opportunity employer. Together we are committed to fostering an environment that is professional, inclusive and diverse. Explore the exciting opportunities currently available in the US and around the world.
Regulatory Affairs Consultant, Orphan Drug We are looking for a Regulatory Affairs Consultant to support several ongoing regulatory submission programs. The support will vary based on the timing of each program but on average could require about 10 hours per week. This role is remote.
Work closely with Pharmatech and our client’s project team to be responsible for the execution of the regulatory operations related to the Lorenz docuBridge TWO submission management software relating to FDA communication and submission of regulatory documentation.
Fast Track and Orphan Drug applications for regulatory submissions to the FDA (or other regulatory agencies)
Participate as part of internal regulatory team to define and execute the regulatory strategy and focus for each program
Support the preparation of briefing packages, and regulatory submission documents as needed, via the Lorenz docuBridge TWO submission management software
Advanced degree from accredited college or university in science, biomedical engineering, plus a minimum of 4 years of experience in Filing Global Regulatory Applications for pharmaceutical and Biotech products using Lorenz docuBridge TWO submission management software
Pharmatech Associates, Inc. provides
equal employment opportunity
to 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
Regulatory Affairs Consultant, Orphan Drug We are looking for a Regulatory Affairs Consultant to support several ongoing regulatory submission programs. The support will vary based on the timing of each program but on average could require about 10 hours per week. This role is remote.
Work closely with Pharmatech and our client’s project team to be responsible for the execution of the regulatory operations related to the Lorenz docuBridge TWO submission management software relating to FDA communication and submission of regulatory documentation.
Fast Track and Orphan Drug applications for regulatory submissions to the FDA (or other regulatory agencies)
Participate as part of internal regulatory team to define and execute the regulatory strategy and focus for each program
Support the preparation of briefing packages, and regulatory submission documents as needed, via the Lorenz docuBridge TWO submission management software
Advanced degree from accredited college or university in science, biomedical engineering, plus a minimum of 4 years of experience in Filing Global Regulatory Applications for pharmaceutical and Biotech products using Lorenz docuBridge TWO submission management software
Pharmatech Associates, Inc. provides
equal employment opportunity
to 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