Senior Clinical Research Clinician & Trial Lead

Pfizer

New Haven (CT)

Vor Ort

USD 139.000 - 232.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

401(k) matching
Retirement contribution
Paid vacation/holiday/personal days
Health benefits (medical, dental, and/

Zusammenfassung

Pfizer Clinical Research Unit seeks a Clinical Research Clinician to act as Investigator and/or Principal Investigator for trials conducted in the PCRU. Provides medical support, consults with clinic physicians, and ensures 24/7 safety coverage for study participants.

As PI or investigator, you will oversee design, conduct, data review, and regulatory submissions, ensuring protocol integrity and high-quality data across Phase I–IV studies.

Qualifikationen

  • Advanced practitioner degree required (APRN).
  • CT license to practice medicine within CT scope.
  • BLS Certification required.
  • Clinical experience of at least 2 years.

Aufgaben

  • Assumes medico-legal scientific integrity and safety oversight for assigned studies.
  • Liaises with Pfizer sites on design, conduct, and progression of PCRU studies.
  • Participates in planning, execution, data review and adverse event coding.
  • Develops informed consent documents and assists in obtaining consent.
  • Oversees conduct of Phase I–IV studies and prepares clinical protocols and reports.
  • Ensures timelines and quality standards for clinical work products.

Kenntnisse

APRN
CT license
BLS certification
leadership

Ausbildung

Advanced practitioner degree (APRN)

Jobbeschreibung

Pfizer Clinical Research Unit seeks a Clinical Research Clinician to act as Investigator and/or Principal Investigator for trials conducted in the PCRU. Provides medical support, consults with clinic physicians, and ensures 24/7 safety coverage for study participants.

As PI or investigator, you will oversee design, conduct, data review, and regulatory submissions, ensuring protocol integrity and high-quality data across Phase I–IV studies.

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