Senior Manager of Regulatory Affairs

Employer
Sirnaomics, Inc.
Location
United States/Remote
Salary
Competitive salary with full benefits
Start date
28 Jul 2022
Closing date
27 Aug 2022

View more

Discipline
Regulatory Affairs
Hours
Full Time
Contract Type
Permanent
Experience Level
Senior Management
You need to sign in or create an account to save a job.

Sirnaomics, Inc. is a leading clinical stage biopharmaceutical company in the discovery and development of RNAi therapeutics for treatment of cancer and fibrotic diseases. We are seeking candidates to fill the newly created position of Sr. Manager of Regulatory Affairs for our headquarters in Gaithersburg, MD.

 

The well-qualified candidate will prepare, track, and assess regulatory documents for submissions, and will be responsible for developing and maintaining templates, files and archives for regulatory correspondence and submissions, in compliance with regulatory affairs department or company policies, practices and procedures.

Requirements & Responsibilities

  • Prepare, track and assess regulatory documents for submissions.
  • Develop and maintain templates, files and archives for regulatory correspondence and submissions, in compliance with regulatory affairs department or company policies, practices and procedures.
  • In collaboration with the Head of Regulatory Affairs, develop functional area practices, policies and procedures and facilitate their implementation.
  • Serve as day-to-day internal operational lead for the assigned Regulatory Affairs functions and project(s) and collaborate with external consultants and vendors to achieve project goals for regulatory affairs activities.
  • Assist in preparing teams for regulatory agency interactions.
  • Prepare INDs, NDAs, CTAs, MAAs, annual reports, amendments and correspondence as well as participating in the development of meeting briefing information and other documents for regulatory agency meetings.
  • Provide document formatting, preparation and quality assessment of documents for regulatory submissions.
  • Identify regulatory issues proactively that may impact the assigned project(s) and discuss strategies to address them with the VP of Regulatory Affairs.
  • In collaboration with the VP of Regulatory Affairs, the Senior manager/Manager will provide the project team(s) for assigned project(s) with advice on potential regulatory affairs requirements, potential issues, regulatory options, procedures and practices based upon research into relevant regulatory requirements and guidance, as well as clinical practice guidance relevant to the preparation and submission of regulatory documentation.  

Education & Experience

  • Bachelor’s degree, or equivalent, in biological science, nursing, pharmacy or related discipline is required.  An advanced degree is preferred.
  • Seven or more years of experience, to include experience managing regulatory submissions and/or projects, to include the management of complex, multi-stakeholder projects and achieving goals is strongly preferred.
  • Regulatory Affairs Certification (RAC) preferred.
  • Demonstrated experience overseeing multiple vendors of various types is desirable.
  • Demonstrated experience in the identification of emerging regulatory risks (consistent with experience).
  • Demonstrated experience collaboratively working within a multi-disciplinary drug development team to help resolve challenges.
  • Excellent written and verbal communication skills (bilingual in Mandarin and English desirable but not required).
  • Demonstrated ability to conduct responsibilities with high level oversight and competency and ability to drive forward work on own initiative.
  • Diplomatic style to drive collaboration in a multi-stakeholder environment.
  • Experience in multi-cultural professional environments.
  • Energetic, service- and goal-oriented style.
  • Develop and maintain excellent knowledge of regulatory procedures and environments; establish rapport and engage with regulatory agencies on project-related matters for assigned project(s), as requested.
  • Stay abreast of the regulatory environment through active participation in conferences and training.

Sirnaomics is an Equal Opportunity Employer, and offers a fast paced/dynamic environment, growth opportunity, competitive compensation and a full benefits program.

Sirnaomics, Inc. is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender-identity, national origin, disability status, protected veteran status, genetic characteristics or any other characteristic protected by law.

Apply for Senior Manager of Regulatory Affairs

Fields marked with an asterisk (*) are required

Your file must be a .doc, .pdf, .docx, or .rtf. No larger than 2MB
Selected file:

Click here to find out more about TopCV

Add a cover message

Your communication preferences

When you apply for a job we will send your application to the named employer, who may contact you. By applying for a job listed on PharmiWeb.jobs you agree to our terms and conditions and privacy policy. You should never be required to provide bank account details. If you are, please contact us. All emails will contain a link in the footer to enable you to unsubscribe at any time.

You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert