Cell No. 4 Interpretation of a cancer cell, provided by Angela Canada Hopkins, daughter of a cancer patient.

Cell No. 4 Interpretation of a cancer cell, provided by Angela Canada Hopkins, daughter of a cancer patient.

Manager/Director, Regulatory Affairs

About Viracta Therapeutics

Viracta Therapeutics is private biotechnology company committed to advancing new medicines to benefit patients with viral-associated cancers and other serious diseases. Viracta’s proprietary platform is a highly targeted combination therapy approach for virus-associated malignancies. Our initial focus is on cancers associated with the Epstein Barr Virus (EBV). We will also expand into additional applications to utilize this approach for a range of cancers and virus-associated diseases.

Position Description:

We are currently seeking a Manager, Regulatory Affairs to join our experienced drug development team in Cardiff, CA. He/she will oversee day to day regulatory activities and contribute to the overall regulatory strategy for the organization and/or for assigned clinical programs. This team member will provide oversight to relevant CROs and consultants in conjunction with the clinical development leadership. We are seeking a strong team player with experience in oncology drug development, strong communication skills, and ability to contribute to a collaborative interdisciplinary environment.

Primary responsibilities of this position include:

Qualifications


Viracta Therapeutics offers an attractive salary and benefits package, including equity incentives. To apply, please submit your resume to info@viracta.com and include the job title in the subject line. No recruiters please.

Manager/Director, Regulatory Affairs

About Viracta Therapeutics

Viracta Therapeutics is private biotechnology company committed to advancing new medicines to benefit patients with viral-associated cancers and other serious diseases. Viracta’s proprietary platform is a highly targeted combination therapy approach for virus-associated malignancies. Our initial focus is on cancers associated with the Epstein Barr Virus (EBV). We will also expand into additional applications to utilize this approach for a range of cancers and virus-associated diseases.

Position Description:

We are currently seeking a Manager, Regulatory Affairs to join our experienced drug development team in Cardiff, CA. He/she will oversee day to day regulatory activities and contribute to the overall regulatory strategy for the organization and/or for assigned clinical programs. This team member will provide oversight to relevant CROs and consultants in conjunction with the clinical development leadership. We are seeking a strong team player with experience in oncology drug development, strong communication skills, and ability to contribute to a collaborative interdisciplinary environment.

Primary responsibilities of this position include:

Qualifications


Viracta Therapeutics offers an attractive salary and benefits package, including equity incentives. To apply, please submit your resume to info@viracta.com and include the job title in the subject line. No recruiters please.