What are the responsibilities and job description for the Regulatory Operations Consultant position at Pharmatech Associates?
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.
Apply below after reading through all the details and supporting information regarding this job opportunity.
We are looking for a Regulatory Operations Consultant to support several ongoing regulatory submission programs. The support will vary based upon the timings of each program but on average could require about 10 hours per week. This role is remote.
Job Duties
- 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.
- Participate as part of internal regulatory team to define and execute the regulatory strategy for each program.
- Support the preparation of briefing packages, and regulatory submission documents as needed, via the Lorenz docuBridge TWO submission management software.
Education and Qualifications
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.
J-18808-Ljbffr
