Senior Medical Director

Atrium Staffing•San Diego, CA

63d•$300,000 - $320,000

About The Position

The Senior Medical Director (SMD) will lead clinical research at a fast-paced integrated research organization. This role combines direct oversight of clinical trials with strategic medical leadership. The SMD will act as Principal Investigator (PI) across various therapeutic areas, ensure studies run safely and smoothly, and build strong relationships with sponsors, CROs, and community partners. This is ideal for a physician with experience in clinical trials and managing adult chronic conditions, who enjoys working in a collaborative and innovative environment.

Requirements

7+ years of healthcare experience in clinical research.
2+ years of FDA-regulated clinical trial experience as a PI or Sub-I.
Strong understanding of medical ethics, GCP, and clinical trial safety.
MD or DO from a U.S.-accredited medical school is required.
Active Board Certification and U.S. medical license.

Nice To Haves

Experience as PI on GLP-1 studies lasting 12+ months.
Clinical trial experience with adult chronic conditions: COPD, Type 2 diabetes, obesity, GLP-1 therapy, movement disorders, psychiatry, pulmonology.
Strong analytical, problem-solving, and organizational skills.
Excellent communication and leadership abilities.
Proficiency in Microsoft Office Suite and clinical trial systems.
Willingness to travel for meetings, audits, and site visits.

Responsibilities

Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials.
Lead all PI responsibilities, including oversight of site staff, patient safety, and regulatory compliance.
Be the main medical contact for sponsors, corporate leaders, and executives.
Ensure trials follow GCP/HSP guidelines, with a focus on safety and data quality.
Help grow research programs and explore new therapeutic areas.
Build partnerships with local doctors and community groups to support recruitment.
Stay updated on therapeutic areas through ongoing learning and conferences.
Review study protocols and materials carefully.
Evaluate study feasibility and site readiness.
Work closely with Operations, Data, and Regulatory teams to ensure smooth execution.
Train and support Project teams and investigators.
Help develop risk assessments and recruitment strategies.
Monitor safety data, patient eligibility, and protocol compliance.
Contribute to strategic planning and tech initiatives.
Ensure compliance with SOPs, GCP, and ethical standards.
Promote a culture of collaboration and scientific excellence.
Provide coaching and feedback to team members.
Track performance and help staff meet goals and deadlines.
Ensure adherence to company policies and legal requirements.
Maintain strong communication across teams.