Assoc. Director, Regulatory Affairs Strategy

Location: Northern

## Assoc. Director, Regulatory Affairs Strategy Apply:
US _North Carolina _Remote:
Full time:
Posted 2 Days Ago:
JR100198
** COMPANY:
*** At Bio Cryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases.
* * We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics. Our global headquarters is in Durham, North Carolina, we have a regional office in Boston, Massachusetts, and our employees span the globe across sites in multiple countries.
* * We are proud of our culture of engagement and accountability that rewards people for innovative thinking and achievement of key objectives. For more information, please visit our website at
* *** or follow us
** on
* * Linked In
* * and
* * Instagram**.
* *
* JOB SUMMARY:

**  ### The Associate Director, Regulatory Affairs Strategy at Bio Cryst Pharmaceuticals (Bio Cryst) will work closely with product development core teams and subteams in setting company goals and work closely with these groups in meeting company goals. This position will be responsible for developing and ensuring efficient and productive regulatory strategies and submissions for Bio Cryst, as well as assisting and collaborating in strategic drug development program implementation.

The position will work to develop and implement key new values and added initiatives focused on the coordination of the company’s regulatory program and product development missions.  
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* ESSENTIAL DUTIES & RESPONSIBILITIES:

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* • With Director of Regulatory Affairs oversight, this position will manage initial global approvals and global post-approval activities for advanced programs working with partnering companies
• Manage and support post-approval maintenance activities for marketed products, including lifecycle management submissions in the US and internationally and support development and early-phase regulatory projects as assigned.
• Support regulatory strategies for assigned projects via researching regulations and guidelines ensuring alignment with regional requirements that will result in the on-time submission and approval of new products.
• Working with Regulatory Operations, compile, prepare and submit IND, BLA/NDA and additional US regulatory filings as necessary to implement the agreed upon strategy.
• May serve as the Global Regulatory Lead (GRL) for defined projects and deliverables that may include, and not limited to, leading identified work streams; attend clinical study team meetings; track and keep reg subteams and program teams current with status of regulatory submissions and any changes in strategies.
• May support GRL for additional programs on defined work streams and deliverables including in the coordination and preparation of Health Authority meetings.
• Review/revise/draft Standard Operational Procedures as required to assure compliance with Global  Regulations and Guidance Documents.
• Manage regulatory timelines and manage/communicate timeline and/or content risks to Director of Regulatory Affairs Strategist or GRL ensuring that regulatory strategies are executed within those approved timelines.
• Maintains current with FDA regulations and guidance regarding INDs, BLAs/NDAs, while developing familiarity with global regulations.
• All other duties as assigned.
** EXPERIENCE &

QUALIFICATIONS:

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* • Bachelor’s degree required with advanced degree (MS; PhD, PharmD) a plus
• Eight (8) to ten years regulatory strategy experience in the biotech/pharmaceutical industry.
• Ability to maintain high ethical standards.
• Excellent organizational skills, attention to details, and communication skills.
• Ability to work as part of a team, both in…