Corey Masten-Legge Email and Phone Number

- Responsible for all in-house legal services including the review of legal issues and advice to clients on appropriate legal action to be taken including commercial/sales/marketing, clinical, medical affairs, manufacturing/distribution/supply chain, regulatory, IT, HR, biometrics, etc. as well as all vendor, service and consulting agreements. Examples include: MSA/SOW/PA, CTA/IST/MTA/CRADA/ICF, DS/DP/FP/3PL, SLA/DPA, etc.- Recent key achievement(s) includes simultaneously supporting an existing international Phase III study (PACIFICA/PAC303), while executing a US commercial ramp up and launch (24 to 120 employees) in less than 12 months (pacritinib/VONJO) and completing start-up of a Phase III clinical trial for COVID-19 and all supporting service and vendor agreements (CRO, pharmacy, radiology, etc) and related clinical trial agreements and informed consent forms in 2 months (PAC319) with 2 FTE.- Oversee Compliance and enterprise level risk assessment and management and company-wide training including C-level and Directors. - Manage the Company’s patent and trademark portfolios and strategy including prosecution, filing and related budget around the Company’s most important compounds.- Due diligence and implementation of major partnerships or acquisitions with SBio (pacritinib/VONJO), Shire/Baxalta (pixantrone/PIXUVRI), Chroma Therapeutics (tosedostat), Spectrum Pharmaceuticals (Zevalin).- Provide legal support for SEC and financial reporting obligations (review of press releases, 10-K’s, 10-Q’s and 8-K’s and auditor support).- Supervise all company litigation (U.S. and international) and related budgets across a variety of matters (Contracts, Securities & Derivative, Employment, Construction, Environmental, etc).- Oversee all company insurance renewal and budget for Property & Casualty and Directors & Officers- Developed and implemented crucial policies and SOP’s (Compliance & Ethics Manual, Record Retention Policy and Schedule, Data Privacy Policy, etc).

Held positions of increasing responsibility - ultimately responsible for all legal matters of the Company and foreign subsidiaries. - Added role of Chief Risk and Compliance Officer overseeing risk assessment and management and compliance across the organization. Implemented Compliance and Ethics policy and training to all employees and Directors. Role reports directly to CEO & Board of Directors.- Oversaw legal services to in-house clients throughout the organization on transactional and contract matters including the review of legal issues and advice to clients on appropriate legal action to be taken, including: license agreements, research and material transfer agreements, consulting agreements, clinical trial agreements, manufacturing and supply agreements, wholesale and distribution, and all company vendor, service and consulting agreements.- Directly responsible for clinical trial agreements for three Phase III international clinical trials with over 150 sites and all related supporting service and vendor agreements.- Completed major partnerships or acquisitions with Shire (formerly Baxter Oncology/Baxalta), SBio, Chroma Therapeutics, and Spectrum Pharmaceuticals, including negotiation and due diligence as well as ongoing partnership activities.- Managed the Company’s patent portfolio; revised and streamlined the patent and trademark strategy and outside counsel around the Company’s most important compounds.- Lead department of one attorney and one administrator. - Successfully managed legal department budget and vendors (8+ years).- Provided legal support for SEC and financial reporting obligations (review of press releases, 10-K’s, 10-Q’s and 8-K’s).- Supervised all company litigation both U.S. and international and related budgets.- Formed new E.U. subsidiary responsible for commercialization of first drug approved in its indication.- Developed and implemented a Corporate Record Retention Policy and Schedule.

Held positions of increasing responsibility - ultimately responsible for all legal matters of the Company and foreign subsidiaries. Reported directly to the Chief Executive Officer.- Oversaw legal services to in-house clients throughout the organization on transactional/contract matters including the review of legal issues and advice to clients on appropriate legal action to be taken, including: license agreements, research and material transfer agreements, consulting agreements, clinical trial agreements, manufacturing and supply agreements, confidentiality agreements, and all company vendor, service and consulting agreements.- Directly responsible for clinical trial agreements for three Phase III international clinical trials with over 150 sites and all related supporting service and vendor agreements.- Completed major partnerships or acquisitions with Baxter Oncology, SBio, Chroma Therapeutics, and Spectrum Pharmaceuticals, including negotiation and due diligence and ongoing partnership activities- Managed the Company’s patent portfolio; revised and streamlined the patent and trademark strategy and outside counsel around the Company’s most important compounds.- Lead department of five staff and successfully managed multi-million dollar budget.- Provided legal support for SEC and financial reporting obligations (review of press releases, 10-K’s, 10-Q’s and 8-K’s).- Supervised all company litigation both U.S. and international- Formed new E.U. subsidiary responsible for commercialization of first drug approved in its indication.- Negotiated all contracts associated with EU product commercialization including: Manufacturing/Supply, Packaging and Labeling, Warehousing and Distribution, Leases, etc. - Served on CTI’s Compliance Committee and gave regular company-wide training on associated legal requirements and risks.- Developed and implemented a Corporate Record Retention Policy and Schedule.

Promoted to Senior Director of Legal Affairs.- Oversaw legal services to in-house clients throughout the organization on transactional/contract matters including the review of legal issues and advice to clients on appropriate legal action to be taken, including: license agreements, research and material transfer agreements, consulting agreements, clinical trial agreements, manufacturing and supply agreements, confidentiality agreements, and all company vendor, service and consulting agreements.- Directly responsible for clinical trial agreements for three Phase III international clinical trials with over 150 sites and all related supporting service and vendor agreements.- Completed major partnerships or acquisitions with Baxter Oncology, SBio, Chroma Therapeutics, and Spectrum Pharmaceuticals, including negotiation and due diligence and ongoing partnership activities- Managed the Company’s patent portfolio; revised and streamlined the patent and trademark strategy and outside counsel around the Company’s most important compounds.- Lead department of five staff and successfully managed multi-million dollar budget.- Provided legal support for SEC and financial reporting obligations (review of press releases, 10-K’s, 10-Q’s and 8-K’s).- Supervised all company litigation both U.S. and international- Formed new E.U. subsidiary responsible for commercialization of first drug approved in its indication.- Negotiated all contracts associated with EU product commercialization including: Manufacturing/Supply, Packaging and Labeling, Warehousing and Distribution, Leases, etc. - Served on CTI’s Compliance Committee and gave regular company-wide training on associated legal requirements and risks.- Developed and implemented a Corporate Record Retention Policy and Schedule.

Promoted to Director and Head of Legal Affairs after 1 year of interim status

Re-took head of department role after replacement VP of Legal Affairs left after 6 months.

Took interim head of department role for six months following VP of Legal Affairs departure and search for new head of department.

• Performed electronic discovery and litigation support. • Reviewed business and legal documents for responsiveness to requests for production. • Identified documents for potential Attorney/Client privilege and assigned protective order designations for documents produced to opposing counsel. • Frequently collaborated with lead attorneys, other eDAT attorneys, and support staff.

Provided legal advice and services for tenants with eviction related issues• Represented tenants at eviction (show cause) hearings• Negotiated with landlords for tenants facing eviction• Helped answer eviction paperwork – provided referrals and resource information