Drug Development Project Manager (NDA Submission/Emerging Biotech) – Top $$/RTP, NC

Job Type: 
Professional Services
Other Professional Positions
Life Sciences
Other Life Science Positions
Employment Category: 
Direct Hire

Our client, a clinical stage biotech that is leveraging its proprietary technology to develop treatments for multiple indications in dermatology, infectious diseases and others, is actively recruiting for a highly capable and knowledgeable candidate to joins its Development team.

This is a hybrid role with a strong focus on Project Management and Regulatory Operations. The company is targeting project managers who have a broad understanding of the entire drug development cycle including knowledge of Regulatory Submission standards and practices. 

This is a critical role for the company and compensation will be generous

Key Things to Note:

  • This company is planning for three potential NDA filings with the first submission expected in Q3 2022.  These are New Chemical Entities (NCE) and this is ground floor opportunity.  Seek candidate who is excited about the science and being part of its build.
  • The focus of the role will be to drive the development and coordination of high-quality regulatory submissions. Seek candidate whose broad knowledge of drug development is complemented by substantial knowledge of regulatory submission standards and practices.
  • The company uses external Regulatory consultants and SMEs to guide regulatory strategy. This Project Manager will coordinate the efforts of these consultants as well as direct all internal operations. Seek candidate who is accustomed to coordinating the work of multiple stakeholders.
  • This individual will be a primary contact for the FDA and other regulatory bodies. Experience communicating with regulatory or other government entities will be important.
  • This is an emerging business setting with a “start-up” vibe.  Seek candidate who enjoys being instrumental in developing and implementing standard operating procedures. Experience implementing enhanced document management systems would be a plus.
  • This is a hybrid role that will split time between the company’s RTP area offices and remote.

Position will involve :

  • working closely with leadership and cross-functional SMEs to support content compilation and finalization, ensure alignment of messaging and oversee submission of final documents
  • leading the organization of and participation in meetings with regulatory agencies, ensuring documentation of discussions, and driving the follow up for resulting regulatory actions
  • overseeing effective and appropriate archival management of regulatory documentation

Selected responsibilities will include

  • Drive content management and integration of content assembled from cross-functional SMEs to support document finalization
  • Plan, coordinate and manage internal preparatory meetings in support of formal regulatory reviews/meetings
  • Create and manage submission plans and ensure coordination of development activities with the submission processes to drive timelines
  • Manage publishing vendors for all regulatory submissions
  • Oversee document publishing for regulatory submissions
  • Oversee management and archival of regulatory records
  • Identify process improvements for internal systems and processes related to publications, submissions and archiving of regulatory documents
  • Maintain awareness of the industry and regulatory developments and support training opportunities to Regulatory Affairs staff on new guidance requirements and submission regulations.

Targeted candidate will offer a BS degree in related science and 10+ years in a biotech/pharma environment, including exposure to Regulatory Affairs matters.  Emerging/start-up company experience is preferred.

Other priorities include:

  • Demonstrated knowledge of FDA and ICH regulations including experience with IND and NDA regulatory submissions
  • Experience in analyzing and developing strategies for clinical development, regulatory submissions, and compliance issues
  • Ability to liaise, negotiate and interact with FDA and worldwide regulatory agencies
  • Exceptional Project Management skills including ability to effectively coordinate the work of multiple, cross-functional stakeholders in a fast-paced, highly dynamic setting.
  • Experience in managing, developing, organizing, and maintaining controlled and noncontrolled files
  • History of growth, impact and longevity

Finally, we seek a highly capable and mission-driven candidate who demonstrates the ability to overcome barriers, work through the ambiguous and earn the respect and cooperation of others in order to achieve shared success.

There is a lot happening and the future is bright.  We seek a leader who is ready and eager to contribute.