Clinical Development Scientist - I&I Studies (Hybrid)

Pfizer

United States

Hybrid

USD 106,000 - 177,000

Full time

6 days ago
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Benefits offered by this job

Hybrid work arrangement
Relocation assistance may be available

Job summary

Pfizer in the United States is seeking a Clinical Development Scientist to support the development and execution of simple to minimally complex clinical studies for small molecule and novel biological therapies in the I&I therapeutic area. You may participate as an individual contributor on clinical study teams and collaborate with Clinical Operations, Biostatistics, and other functions.

You will work with study sub-teams to ensure collaboration, data review, and timely study delivery.

Qualifications

  • PharmD/PhD or MS/MA/MSN with 2+ years of related industry clinical study experience OR BS/BA/BSN with 4+ years of related industry clinical study experience.
  • Comprehensive knowledge of GCP and ICH guidelines.
  • Strong communication and interpersonal skills.

Responsibilities

  • Support the development and execution of simple to minimally complex clinical studies; assist senior staff on more complex studies.
  • Support preparation and review of study documents including protocols, consent forms, and study training materials.
  • Assist clinician data review activities and safety data collection for review meetings.
  • Provide technical support for clinical issues in collaboration with the Global Development Lead.
  • Collaborate with the study team to maintain open communication and support study completion.

Skills

GCP & ICH knowledge
Strong communication
Microsoft Office

Education

PharmD/PhD or MS/MA/MSN with 2+ years OR BS/BA/BSN with 4+ years experience

Tools

Microsoft Office Suite

Job description

Pfizer in the United States is seeking a Clinical Development Scientist to support the development and execution of simple to minimally complex clinical studies for small molecule and novel biological therapies in the I&I therapeutic area. You may participate as an individual contributor on clinical study teams and collaborate with Clinical Operations, Biostatistics, and other functions.

You will work with study sub-teams to ensure collaboration, data review, and timely study delivery.

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