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 Pediatrician for a Principal or Sub-Investigator role at our Tustin, CA site location. Prior research experience is not required. The investigator should be actively practicing and will be able and willing to refer patients to studies. As a Pediatric Principal or Sub-Investigator at our clinical research site, you will play a vital role in advancing medical knowledge and improving patient care. You will be responsible for ensuring the successful execution of research protocols, patient safety, maintaining compliance with regulatory requirements, and contributing to the growth and success of our research site. This contractor position offers the opportunity to make a significant impact in the field of clinical research with the potential for increased involvement as study demand grows. This is a partnership opportunity to conduct clinical research with Tilda Research where Tilda will provide Investigators with facilities, staff, systems, and business development.
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 able to 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:
- Excellent verbal and written communication skills.
- Excellent organizational skills and attention to detail.
- Excellent time management skills with a proven ability to meet deadlines.
- Strong analytical and problem-solving skills.
- Strong supervisory and leadership skills.
- Ability to prioritize tasks and delegate them when appropriate.
- Ability to function well in a high-paced environment.
Education and Experience:
- Medical degree (MD or DO) with board certification in Pediatrics.
- Active medical license in California.
- Actively practicing as a Pediatrician.
- Prior research experience is not required.
