Description
You will support the development and execution of one or more less complex studies for small molecule and/or novel biological therapies in the Infectious Diseases and Immunology (I&I) therapeutic area.
You may participate as an individual contributor on clinical study teams to support enrollment and study delivery timelines, working with other functional disciplines as needed.
Your responsibilities will include:
- Supporting the development and execution of simple to minimally complex clinical studies
- Preparing and reviewing study-related documents, such as clinical protocols and informed consent documents
- Supporting clinician data review activities and collecting safety data for safety review meetings
- Providing technical support for clinical issues raised by internal and external collaborators
- Collaborating with the study team to maintain open communication and support successful study completion
The minimum qualifications for this role are:
- PharmD/PhD in a related discipline, 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
- Good understanding of the pharmaceutical/biopharmaceutical environment and drug development
- Strong communication and interpersonal skills
- Proficiency in Microsoft Office applications, including Word, PowerPoint, and Excel
Preferred qualifications include experience in a clinician-type role or clinical operations-type role, as well as project management experience.
The annual base salary for this position ranges from $106,000.00 to $176,600.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan and share-based long-term incentive program. Pfizer offers comprehensive benefits, including a 401(k) plan, paid vacation, and health benefits.