Principal Investigator

Job Description

Job Description

Celerion is committed to swift, exceptional clinical research through translational medicine.  Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.

The PI is responsible for the safety of subjects who participate in clinical trials and for executing the study according to the IRB-approved protocol and applicable FDA and GCP regulations.

Pre-Study :

• Review protocol and Investigator Brochure for subject safety, scientific, and operational feasibility of study.  Provide input to sponsor as indicated.
• Complete FDA 1572 and financial disclosure forms.
• Attend study initiation meetings with sponsor.
• Communicate with Institutional Review Board during protocol approval process and subject safety issues.
• Explain study to subject and answer questions, ensure proper consent, and perform screening examination.
• Final review of all screening data and authorization of subjects to be enrolled in the study.

During / Post Study :

Additional Responsibilities :

Qualifications

Celerion Values :        Integrity   Trust   Teamwork   Respect

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.