PIERRE v. OTSUKA AMERICA PHARMACEUTICALS

CourtDistrict Court, D. New Jersey
DecidedApril 19, 2024
Docket3:23-cv-21848
StatusUnknown

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

Bluebook
PIERRE v. OTSUKA AMERICA PHARMACEUTICALS, (D.N.J. 2024).

Opinion

NOT FOR PUBLICATION

UNITED STATES DISTRICT COURT DISTRICT OF NEW JERSEY

MIRRIAM PIERRE, Plaintiff, Civil Action No. 23-21848 (MAS) (DEA) Vv. MEMORANDUM OPINION OTSUKA AMERICA PHARMACEUTICALS, Defendant.

This matter concerns alleged retaliation in violation of the New Jersey Conscientious Employee Protection Act (the “CEPA”), N.J. Stat. Ann. § 34:19-1 e¢ seg. Currently before the Court are two motions: one by Defendant Otsuka American Pharmaceutical Development & Commercialization Inc. (“Otsuka” or “Defendant”)! to dismiss Plaintiff's Amended Complaint under Federal Rule of Civil Procedure’ 12(b)(6) (ECF No. 20), and one by Plaintiff Mirriam Pierre (“Plaintiff”) to remand this case to the Superior Court of New Jersey, Somerset County (ECF No. 7). The Court has considered the parties’ moving, opposition, and reply papers, and decides the matter without oral argument pursuant to Local Civil Rule 78.1. For the reasons stated below, Plaintiff's Motion to Remand is denied. Defendant’s Motion to Dismiss is granted.

' Defendant states that it has been improperly named in the Complaint as “Otsuka America Pharmaceuticals.” (Def.’s Opp’n Br. 1, ECF No. 9.) Neither party has moved to amend the caption to date. Unless otherwise noted, all references to “Rule” or “Rules” hereinafter refer to the Federal Rules of Civil Procedure.

I. BACKGROUND A. Factual Background The following facts are derived from the Amended Complaint.? (Am. Compl., ECF No. 17.) Plaintiff was employed with Otsuka as a Senior Director and Head of Data Management from December 2020 until January 2023. (/d. {J 6-7.) Otsuka is a pharmaceutical company that develops health products and pharmaceutical drugs to treat various diseases and health conditions. (/d. 18-19.) While employed with Otsuka, Plaintiff was assigned to a group responsible for handling data of pre-market drugs to ensure the integrity of Otsuka’s database in preparation for clinical trials. dd. 20-22.) Specifically, Plaintiff's group “collected, cleaned|,| and locked data” for all of Otsuka’s clinical trials from December 2020 to January 2023. Ud. § 20.) At the start of Plaintiff’ s employment, her group was comprised of 15 members and tasked with handling 14 clinical trials. (id. □ 26.) By January 2023, Plaintiff was responsible for 37 clinical trials, but her group dwindled to 9 members. (/d. § 27.) This reduction in headcount is alleged to have “affected the quality of data being collected, cleaned[,] and locked.” Ud. ¥ 28.) Beginning in the summer of 2022, Plaintiff made monthly presentations to Otsuka’s Research and Development Team (“RDLT”) to address certain issues that were affecting the group. (/d. Jf 9-15.) These issues included, among other things: (1) “Otsuka’s decision to refuse approval for [an] adequate headcount” which compromised “[Plaintiff’'s] department’s ability to ensure data integrity”; (2) “Otsuka’s database lock period was unreasonably short and objectively shorter than industry standard”; (3) Otsuka’s “site lock process” jeopardized “patient safety and

3 The Court, as it must, accepts as true all of Plaintiff's well-pleaded factual allegations and “construe[s] the complaint in the light most favorable to [P]laintiff.” Fowler v. UPMC Shadyside, 578 F.3d 203, 210 (3d Cir. 2009) (citation omitted).

data integrity”; and (4) Otsuka’s failure to disclose adverse events risked presenting misleading data to regulatory authorities such as the Food and Drug Administration (“FDA”). Ud. ¥§ 10-15.) Plaintiff states that, as these issues surfaced, members of the RDLT became “increasingly upset” and Plaintiff was “aggressively questioned” on the information she was presenting during the RDLT meetings. (/d. {4 81-82.) Plaintiff alleges that she was asked by two individuals outside of the RDLT “not to continue to raise these issues.” (/d. { 83.) Based on Plaintiff's ongoing concerns regarding the “implications on patient health and safety that could arise from improperly cleaned and locked datal,]” Plaintiff “continued to raise these concerns” with the RDLT—all of which went unanswered. (/d. [ff 89, 91-92.) According to Plaintiff, this caused Otsuka’s leadership team to become “increasingly hostile and aggressive towards [Plaintiff] with the hopes that they could push her to quit her job.” (id. € 93.) Specifically, it is alleged that two members of the leadership team, Carol Augustine (“Augustine”) and Debbie Profit (“Profit”) retaliated against Plaintiff by engaging in conduct that included, but was not limited to: stating that Plaintiff was “not capable of performing the role of [Senior] Director[,]” isolating Plaintiff from her peers by stating she was a “‘bad’ employee”, creating a culture which excluded those who objected to the status quo, making disparaging comments about Plaintiff, and “repeatedly humiliat[ing] Plaintiff in meetings by minimizing the evidence [Plaintiff] provided on the data issues found.” Ud. 83, 110-23.) Because Plaintiffs group remained “understaffed” and in light of ongoing concerns over the “risky professional position that Otsuka had put her in,” Plaintiff states that she had no option but to resign from her position with Otsuka in January 2023. (/d. {| 94.)

B. Procedural History Several months after Plaintiff's resignation, in October 2023, this action was filed in the Superior Court of New Jersey, Somerset County (“State Court”) alleging a single claim against Defendant under the CEPA. (See State Court Complaint, annexed to Notice of Removal, Ex. A, ECF No. 1-1.) Defendant timely removed this action in November 2023.4 (See Notice of Removal, ECF No. 1.) The instant motions followed. I. LEGAL STANDARD A. Remand A motion to remand is governed by 28 U.S.C. § 1447(c), which provides that a case removed to federal court shall be remanded “[i]f at any time before final judgment it appears that the district court lacks subject matter jurisdiction.” After a matter is filed in state court, a defendant may remove any action over which the federal courts have jurisdiction. 28 U.S.C. § 1441(a). The party removing the action has the burden of establishing federal jurisdiction. Stee! Valley Auth. v. Union Switch & Signal Div., 809 F.2d 1006, 1010 (3d Cir. 1987). Removal statutes are “strictly construed against removal and all doubts should be resolved in favor of remand.” Jd. For removal to be proper, a federal court must have original jurisdiction; that is, the removed claims must arise from a “right or immunity created by the Constitution or laws of the United States[,]” or there must be complete diversity between the parties. Concepcion v. CFG Health Sys. LLC, No. 13-2081, 2013 WL 5952042, at *2 (D.N.J. Nov. 6, 2013); see also 28 U.S.C. § 1332. To satisfy the jurisdictional requirements of 28 U.S.C. § 1332(a)(1), the federal diversity statute, no plaintiff can be a citizen of the same state as any of the defendants and the amount in

* Plaintiff's Amended Complaint followed the Notice of Removal and was filed on December 15, 2023. (See Am. Compl.)

controversy must exceed $75,000.00. Carden v. Arkoma Assocs., 494 U.S. 185, 187 (1990); Schneller ex rel.

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PIERRE v. OTSUKA AMERICA PHARMACEUTICALS, Counsel Stack Legal Research, https://law.counselstack.com/opinion/pierre-v-otsuka-america-pharmaceuticals-njd-2024.