Research Medical Director (Part TIme) – Maitland, FL Position Available In Orange, Florida

Research Medical Director (Part TIme) – Maitland, FL Advanced Dermatology and Cosmetic Surgery – 2.4

Maitland, FL Job Details Part-time Estimated:

$194K – $270K a year 19 hours ago Qualifications Medicine Management Clinical research

BC/BE HIPAA 3

years Quality assurance Dermatology Patient care Clinical trials Typing Phone etiquette Senior level Medical terminology Communication skills Full Job Description Join a workplace recognized by Newsweek as America’s Greatest Workplaces for 2024. Advanced Dermatology and Cosmetic Surgery’s mission is to deliver the highest quality patient care and experience in dermatology and aesthetic services. The Medical Director of Clinical Research is responsible for providing clinical and medical expertise across all phases of clinical trials. Working in close partnership with the Clinical Research Administrator, this role ensures patient safety, protocol integrity, data quality, and compliance with regulatory and ethical standards. The role serves as a key liaison between the investigators and cross-functional teams to support the successful execution of clinical trials.

KEY RESPONSIBILITIES

Medical Oversight & Patient Safety Serve as the primary medical contact for clinical trial sites and safety queries. Conduct ongoing medical review of clinical trial data, including adverse events (AEs), serious adverse events (SAEs), and protocol deviations. Ensure timely medical assessment and reporting of safety data to internal and external stakeholders. Alongside the Clinical Research Administrator, ensure trials are conducted in accordance withICH-GCP, local regulations, and internal SOPs. Support preparation and review of clinical and safety sections of regulatory documents (e.g., INDs, CTAs, CSRs). Maintain awareness of current dermatologic clinical practice and evolving regulatory expectations related to dermatology studies. Protocol Development & Scientific Leadership Provide medical insight during protocol feasibility and site selection processes. Review medical components of clinical study documents, including the Investigator Brochure (IB), Clinical Study Report (CSR), and Informed Consent Forms (ICFs). Provide guidance on the use of clinical photography, lesion tracking, histopathology requirements, and biomarker collection (e.g., skin biopsies). Review subject enrollment eligibility and diagnostic accuracy of dermatologic conditions. Cross-functional Collaboration Work closely with clinical operations, data management, and compliance teams Participate in clinical trial team meetings and provide medical expertise throughout the trial lifecycle. Support training of clinical site staff and internal teams on the medical and scientific aspects of the study. Regulatory & Ethical Compliance Ensure studies are conducted in accordance with ICH GCP, local regulations, and company SOPs. Support regulatory filings, including IND/CTA submissions and responses to health authority queries. Contribute to the development of safety narratives and clinical sections of regulatory documents.

KNOWLEDGE, SKILLS, AND ABILITIES

Knowledge of ADCS policies, including quality assurance policies and applicable government regulations and standards, and the ability to actively apply that knowledge in the performance of all job duties Knowledge of electronic health record access-level privileges and responsibilities, and the ability to perform electronic health record job duties for this position within the parameters of the access level assigned Ability to practice confidentiality and follow HIPAA regulations with patient information Ability to practice professional ethics and use discretion concerning ADCS directives and proprietary information/trade secrets of the organization Ability to recognize a problem and effectively problem-solve, using guidance from the provider and/or management when necessary Knowledge of medical terminology and ability to use appropriately Ability to manage time efficiently, prioritize, multi-task, and adapt to change Ability to maintain high level of accuracy in all documentation and in the performance of all job duties Ability to perform the essential job duties within the scope of education and training Skilled in typing/keyboarding; skilled in using computers

PROFESSIONALISM

Project a professional manner and image, including proper workplace attire and grooming standards; exhibitprofessional conduct at all times Adhere to ethical principles and core ADCS values; follow all ADCS policies Treat all patients and staff with respect, compassion, and empathy, recognizing and respecting cultural diversity Demonstrate initiative and responsibility for actions Work as an effective team member Maintain a strong record for attendance and punctuality in arriving at work Enhance skills through continuing education

Education:

MD, DO, or equivalent medical degree; board certification preferred.

Experience:

Minimum 3-5 years of clinical research experience Prior experience as a clinical research physician strongly preferred.

LANGUAGE/COMMUNICATION REQUIREMENTS

Ability to read and interpret work-related documents such as reports, communications, safety rules, operating and maintenance instructions, and procedure manuals Ability to write routine reports and correspondence Ability to listen, speak, and interact effectively with all patients and co-workers, adapting communication for optimal understanding Ability to practice professional telephone etiquette and techniques on all calls

MATHEMATICAL SKILLS

To the extent necessary for the performance of the job duties of a Medical Assistant – such as pharmacology-related job duties (mixing medications, Botox, lidocaine, etc.) – the ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals.

REASONING ABILITY

Ability to understand and follow instructions, both written and verbal. Must possess strong problem identification/resolution skills and be able to manage complications involving several variables.

WORK ENVIRONMENT AND CONDITIONS

Work is performed in a medical clinic and offices. Involves frequent telephone and in-person contact with patients, staff, vendors, providers, and management. Requires some flexibility in working hours. Requires the ability to work in a demanding environment and to effectively resolve conflicts as they arise. Occasional weekend work may be required. Occasional travel to clinical sites, investigator meetings, or conferences may be required.

PHYSICAL DEMANDS

Work requires sitting with prolonged periods of walking and standing. Tasks require grasping, fine finger and hand dexterity, and computer keyboarding and mouse usage. This position requires that the employee be able to push/pull, reach, bend, and kneel/crouch/squat. Occasional lifting up to 25 pounds. Normal vision required, with or without corrective lenses. Normal hearing is required.