Dermatologist, Principal Investigator - PRN/Part Time - Pleasanton, CA

 By embedding high-quality research within local communities, Hawthorne makes clinical trials more accessible and convenient for patients. Our community-based model shortens timelines and helps bring better treatments to market, faster.

Hawthorne Health is Seeking a Dermatologist (1099 | PRN) to support upcoming clinical trials in Pleasanton, CA. This is a flexible, supplemental opportunity for a physician who’s interested in contributing to research alongside their clinical work. Prior clinical research experience is strongly preferred, and hands-on injection experience is required. You’ll help ensure high-quality participant care and protocol execution while gaining (or expanding) valuable, sponsor-backed clinical research experience.

Responsibilities
• Perform and document protocol-required aesthetic injections (e.g., injectables/dermal fillers/neuromodulators as applicable), ensuring precise technique, participant safety, and adherence to study-specific dosing and administration guidelines.
• Document findings and contribute to ongoing clinical trials, registries, or research protocols as applicable.
• Oversee and manage all aspects of clinical trials conducted at the research site, ensuring adherence to the study protocol, Good Clinical Practice (GCP), ICH guidelines, and all applicable regulatory requirements.
• Lead and supervise the clinical research team, including sub-investigators, study coordinators, and other site staff.
• Delegate study-related duties appropriately to qualified personnel and ensure proper training and oversight.
• Conduct remote review of patient assessments, including physical exams, medical histories, and eligibility screenings, to ensure appropriate participant enrollment.
• Review and interpret laboratory results, ECGs, and other diagnostic tests.
• Make critical medical decisions regarding participant care, adverse events, and protocol deviations.
• Ensure accurate, complete, and timely collection and documentation of all study data.
• Communicate effectively with sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), and regulatory authorities.
• Manage investigational product accountability, storage, and administration according to protocol and with the help of the on-site IP team.
• Participate in site initiation visits, monitoring visits, audits, and inspections.
• Maintain continuous medical education and stay current with advancements in clinical research and relevant therapeutic areas.

Requirements
• Experience as a Principal Investigator on at least 3 sponsor initiated clinical trials preferred.
• Medical Doctor (M.D. or equivalent) degree from an accredited institution.
• Current, unrestricted medical license in California.
• Board certification in Dermatology.
• Demonstrated in-depth knowledge of ICH-GCP guidelines, FDA regulations, and other relevant ethical and regulatory requirements for clinical research.
• Proven leadership and team management skills.
• Excellent clinical judgment and decision-making abilities.
• Strong verbal and written communication skills in English, with the ability to present complex information clearly and concisely.
• Exceptional organizational skills and meticulous attention to detail.
• Ability to manage multiple complex studies simultaneously and prioritize tasks effectively.
• Commitment to ethical conduct and patient safety.