Clinical Development Scientist — Hybrid, Early-Stage Trials

Pfizer; Cambridge (MA); Hybrid; USD 106.000 - 177.000; Vollzeit

Benefits dieser Stelle

Relocation support

Comprehensive benefits package

Zusammenfassung

Pfizer is seeking a Clinical Development Scientist to support development and execution of one or more studies in the I&I therapeutic area. This role operates on a hybrid on-site schedule and requires authorization to work in the United States.

You may contribute as an individual contributor or mentor others on clinical study teams, collaborating with operations, medical monitors, biostatistics, and other functions to meet enrollment and delivery timelines.

Qualifikationen

• Comprehensive knowledge of GCP and ICH guidelines.
• Good understanding of the pharmaceutical/biopharmaceutical environment and drug development.
• Proficiency in Microsoft Office applications, including Word, PowerPoint, and Excel.

Aufgaben

• Support development and execution of simple to minimally complex clinical studies; assist senior team members as needed.
• Assist in preparing and reviewing study documents (protocols, informed consent, training materials).
• Support clinician data review activities and safety data collation for review meetings per the data review plan.
• Provide technical support for clinical issues raised by collaborators in collaboration with the Global Development Lead.
• Collaborate with study team to maintain open communication and support successful study completion.

Kenntnisse

Strong communication and interpersonal

Microsoft Office (Word, PowerPoint,-EX

Ausbildung

PharmD/PhD in a related discipline

MS/MA/MSN with 2+ years clinical study experience

BS/BA/BSN with 4+ years clinical study experience

Jobbeschreibung

Pfizer is seeking a Clinical Development Scientist to support development and execution of one or more studies in the I&I therapeutic area. This role operates on a hybrid on-site schedule and requires authorization to work in the United States.

You may contribute as an individual contributor or mentor others on clinical study teams, collaborating with operations, medical monitors, biostatistics, and other functions to meet enrollment and delivery timelines.