Yancy v. Azar

CourtDistrict Court, D. Maryland
DecidedSeptember 16, 2021
Docket8:20-cv-00276
StatusUnknown

This text of Yancy v. Azar (Yancy v. Azar) is published on Counsel Stack Legal Research, covering District Court, D. Maryland primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Yancy v. Azar, (D. Md. 2021).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF MARYLAND

: HAILE F. YANCY, PHD. :

v. : Civil Action No. DKC 20-0276

: XAVIER BECERRA,1 IN HIS OFFICIAL CAPACITY AS SECRETARY : OF THE DEPARTMENT OF HEALTH AND HUMAN SERVICES :

MEMORANDUM OPINION Presently pending and ready for resolution in this employment case is a motion to dismiss or for summary judgment filed by Defendant, Xavier Becerra, Secretary of the United States Department of Health of and Human Services (“HHS” or the “Agency”). (ECF No. 11). The issues have been fully briefed, and the court now rules, no hearing being deemed necessary. Local Rule 105.6. For the reasons that follow, Defendant’s motion will be granted. I. Background Plaintiff, Haile F. Yancy, is an African American research biologist in the Office of Research (“OR”) within the Center for Veterinary Medicine (“CVM”), a division of the Food and Drug Administration (“FDA”). For most of the time relevant, Dr. Mary

1 The complaint named Alex M. Azar II, former Secretary of Health and Human Services (“HHS”) as Defendant. (ECF No. 1). Xavier Becerra now serves as HHS Secretary. Pursuant to Fed.R.Civ.P. 25(d), Secretary Becerra is automatically substituted as a party to this action. Allen served as Plaintiff’s direct supervisor, and Dr. John Graham served as Plaintiff’s second-level supervisor. Dr. Michael Myers became Plaintiff’s first-level supervisor in early 2016. During his twelve-year career at CVM, Plaintiff invented a DNA sequence used to create a “primer” that detects contaminants in animal feed.

Plaintiff’s OR lab would manufacture and provide the primers to several other labs within CVM’s Office of Regulatory Affairs (“ORA”), which used the primers to conduct regulatory testing on commercial products. During the relevant time period, Plaintiff was also involved in multiple research studies and technology transfer agreements (“TTAs”). TTAs allow FDA scientists to develop new technologies in collaboration with private industry partners. Both sides may contribute funds, personnel, facilities, and equipment. If the technology is then licensed by the private company for commercialization, the Agency is entitled to collect royalties, a portion of which go directly to the inventor. There are two types

of TTAs: Cooperative Research and Development Agreements (“CRADAs”) and Research Collaboration Agreements (“RCAs”). Plaintiff had two open CRADAs in place with BioGX and InstantLabs and one draft CRADA with Qiagen not yet executed. Despite FDA scientists’ ability to license inventions with Agency approval, all such inventions belong to the government. In November 2013, Dr. Graham became the OR Director and later implemented a series of reforms. In September 2014, he instituted a policy requiring that all TTAs be connected to an approved research study. He also began a department-wide “triage process” subjecting all research studies to review. Multiple reviewers

assessed the research studies for criteria designed to determine whether the studies remained relevant to OR’s strategic mission and its current client needs. If the study or a connected TTA failed to satisfy the criteria, it would be cancelled. Plaintiff filed two prior Equal Employment Opportunity (“EEO”) complaints on an undisclosed date presumably prior to November 2013.2 Both complaints were fully resolved by a settlement agreement dated September 18, 2015. A. Review & Cancellation of CRADAs On October 20, 2015, Dr. Graham emailed Plaintiff requesting the study numbers related to his CRADAs. On November 10, 2015, Dr. Graham informed the four OR scientists with open CRADAs or RCAs of the criteria that would be used to assess their TTAs. It

was ultimately determined that Plaintiff’s CRADAs were not sufficiently relevant to OR’s mission. Dr. Graham made attempts

2 Plaintiff does not provide the date he made either EEO complaint or attach copies of them. He does, however, state that “Dr. Graham was informed of the existence of [the] complaint around the time he entered into the [Director] position in November 2013.” (ECF No. 1-1, at 3). This implies he made such complaints prior to November 2013. to find other departments to house Plaintiff’s CRADAs but was unsuccessful. In April 2017, Plaintiff’s BioGX and InstantLabs CRADAs were cancelled and his draft Qiagen CRADA was closed. The other three scientists’ agreements were reviewed but not cancelled.3 Plaintiff alleges that the Agency’s new requirement

that a CRADA be tied to a study was instituted by Dr. Graham to retaliate against him for his prior EEO activity. B. Internal Disclosure of Primer Sequence In January 2016, Dr. Graham determined that it was not within OR’s purview to provide primers to ORA for regulatory testing because ORA received funding to procure such materials and because the process OR was using to produce the materials was not subject to adequate quality control procedures. Effective April 2016, Dr. Graham stated that OR would no longer produce the primers for ORA but would instead provide it with the primer sequence so that it could produce and pay for the materials itself. C. Review & Cancellation of Plaintiff’s Research Studies In September 2016, Plaintiff was notified that fourteen of

his research studies would be cancelled for failure to meet the assessment criteria. Plaintiff alleges that his studies were

3 The race of the other scientists whose TTAs were reviewed is not stated. cancelled in retaliation for his prior EEO activity. In total, 100 out of 130 studies evaluated were terminated.4 D. Failure to Endorse for Promotion In order to receive a non-competitive promotion to the general schedule (“GS”) 15 level, research scientists within CVM must undergo peer review. Under this process, a candidate must submit

a peer review package to his immediate supervisor for review and concurrence. If the immediate supervisor does not concur, the candidate and supervisor attempt to discuss and resolve differences in the package. If the differences cannot be resolved, the candidate may submit a self-nomination package without managerial support. In February 2016, Plaintiff submitted a peer review package for promotion to GS-15 to Dr. Allen. Dr. Allen reviewed the package and informed Plaintiff that she would not endorse it. Plaintiff and Dr. Allen were scheduled to meet to discuss his package on April 7, 2016 but shortly after the meeting was scheduled to begin, Plaintiff cancelled at the advice of his

attorney and the EEO office. Plaintiff had instead initiated the peer review process by self-nomination on March 22, 2016. Before the self-nomination package was processed, however, it was forwarded to Dr. Graham for endorsement as Plaintiff’s second-

4 The race of the other scientists whose research studies were cancelled is not stated. level supervisor. On April 26, 2016, Dr. Graham notified Plaintiff that he also would not endorse his package. Plaintiff’s self- nomination package was then forwarded to the Peer Review Committee for review. At Plaintiff’s request, a colleague served as the in-depth

reviewer of his promotion package. The colleague interviewed Plaintiff’s first-level supervisor at the time, Dr. Myers, as part of her review. A summary of her findings was presented at the Peer Review Committee meeting on July 11, 2016. The Committee gave Plaintiff a score of 40 points, which falls within the range for a GS-14-level position (36 to 42 points). The CVM HR Specialist for Plaintiff’s review concurred with the appraisal. Plaintiff was notified in December 2016 that he was not promoted. On March 1, 2016, Plaintiff initiated contact with an EEO counselor.

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