Sub- Investigator / Nurse Practitioner (Clinical Research)

Why work at Tilda?

Our Mission!

Tilda exists to accelerate the development of new medical treatments by providing every person easy access to clinical trials. As a tech-enabled clinical trial network, we build software and services to help pharma innovators better execute their clinical trial programs. Our work leads to faster cures and thus institutes a meaningful impact on millions of lives. You can help us realize that goal.

Who are we?

Tilda Research is an innovator in clinical research recruitment and trial execution. We operate a growing network of clinical research sites in the US, and our team has worked on over 250 pan-indication Phase I through IV studies. Our founders are successful serial entrepreneurs, with three of their past companies leading to IPOs (VMware, MobileIron) or exits (LexentBio acquired by Roche). We also build software and support clinical trial infrastructure to help pharmaceutical companies identify, enroll, and execute clinical trials efficiently.

Who are you?

We are seeking a practicing Nurse Practitioner for a Sub-Investigator role at our Birmingham, AL site location. Prior research experience is not required . The investigator should be actively practicing and be willing and able to refer patients to studies.

Duties and Responsibilities :

• Conduct pediatric clinical research in accordance with research protocols and ethical guidelines
• Ensure the safety and well-being of all pediatric participants in the study at the trial site
• Actively practice pediatrics and refer eligible patients to research studies
• Collaborate with the Principal Investigator and research teams to support the successful execution of studies
• Review and adhere to study protocols
• Participate in monitoring visits and sponsor meetings
• Maintain proper documentation
• Ensure that the study, consent, and other documents provided to the subjects are approved by the Institutional Review Board (IRB) and comply with Good Clinical Practice (GCP) and other regulatory requirements.
• Provide access to research-related records to monitors, auditors, representatives of the IRB, and regulatory authorities.

Required Skills and Abilities :

Education and Experience :

$57 - $75 an hour

Compensation depends on negotiated rates for each study. The compensation can range from $57.00 to $75.00 Per Deim