We are seeking an experienced Clinical Research Director to join our team at Tilda Research Inc. as a Principal Investigator for our Birmingham, AL site.

• Protocol Execution: Ensure the successful execution of research protocols, maintaining compliance with regulatory requirements and contributing to the growth and success of our research site.
• Partnership Opportunity: This is a partnership opportunity to conduct clinical research with Tilda Research, where we will provide Investigators with facilities, staff, systems, and business development.

• Medical Direction: Provide overall medical direction and medical review of protocols in conformance with the investigational plan and good clinical practice.
• Feasibility Assessments: Provide medical and scientific feasibility assessments for all new sponsor inquiries.
• Participant Safety: Ensure that the safety and well-being of all participants in the study at the trial site are protected.
• Data Integrity: Ensure that data collected at the study site is credible and accurate.
• Participant Rights: Ensure the rights, integrity, and confidentiality of all participants in the trial at the site are protected.
• Monitoring and Auditing: Participate in monitoring visits and sponsor meetings; allow monitoring and auditing by sponsors and inspection by appropriate regulatory agencies.
• Study Procedures: Perform physical assessments and study procedures, review participants' medical history, administer Investigational Product, and review and adhere to the study protocol.
• Documentation: Ensure accuracy, completeness, legibility, and timeliness of data reported on the CRF (case report form) and be consistent with source documents.
• Reporting: Immediately report Serious Adverse Events (SAEs) or any abnormalities affecting participants' safety to sponsors and the IRB as per specific reporting guidelines.
• Regulatory Compliance: Maintain proper documentation, ensure that the study, consent, and other documents provided to the subjects are approved by the IRB and comply with GCP and other regulatory requirements.

• Medical Degree: Medical degree (MD or DO) with board certification in Internal Medicine or Family Medicine.
• Active Medical License: Active medical license in California.
• Clinical Research Experience: Clinical research experience is required with a minimum of 10 completed studies.

• Business Development: We liaise with sponsors to secure studies for you.
• Facilities and Equipment: Modern infrastructure ready for any clinical trial.
• Dedicated Staff: Our team includes Clinical Research Coordinators (CRCs), Research Associates (RAs), Nurses, Pharmacists, and more, ready to support you.
• Advanced Systems: Tilda has a proprietary technology system for executing trials end-to-end that prioritizes automation, increases flexibility (e.g., the ability to review visits remotely), and minimizes administrative work for investigators.