Medical Director – General Medicine

This is a fully remote position, open to applicants in United States.

📋 Description

• Deliver medical, clinical, and scientific advisory insights across various therapeutic areas, such as Immunology, Pain Management, Neurology, and/or Respiratory.

• Act as a Medical Advisor for designated projects.

• Offer medical assistance to investigative sites and project personnel regarding protocol-related concerns.

• Evaluate and clarify trial-related Adverse Events (AEs) and their coding.

• Perform medical case assessments of Serious Adverse Events (SAEs), including documentation and patient narratives.

• Review medical aspects of protocols, Investigative Drug Brochures (IDBs), and/or Case Report Forms (CRFs).

• Conduct medical evaluations of Clinical Study Reports (CSRs), patient narratives, marketing applications, clinical safety/efficacy summaries and overviews, along with other significant documents.

• Function as a Scientific Advisor, providing guidance to Project Managers on medical and scientific elements of assigned projects.

• Engage in the development of the Medical Monitoring section of client proposals, including budgeting considerations.

• Aid Business Development by analyzing and offering medical/scientific feedback on Requests for Proposals (RFPs).

• Participate as a Rho representative during bid defenses and various sponsor meetings.

• Assist in feasibility activities as needed.

• Collaborate with senior management, customers, and project teams to guarantee the safety of clinical-trial subjects and uphold the scientific and ethical integrity of trial design and execution.

• Provide medical insights into clinical programs and contribute regulatory input as required.

⛳️ Requirements

• A medical degree from an accredited medical institution.

• Active medical license in good standing, or previously held.

• Over 5 years of experience in clinical medicine beyond residency training.

• More than 5 years of clinical development experience, preferably within the pharmaceutical sector or a closely related field.

• Strong understanding of research methodologies and clinical trial design, including biostatistics.

• Solid grasp of scientific and ethical regulations and guidelines relevant to clinical research, including knowledge of federal drug development regulations.

• Capability to establish and manage multiple concurrent priorities, deadlines, and strategic departmental goals and objectives.

• Proficient in providing consultation and advice across various assignments.

• Demonstrated initiative and adaptability.

• Ability to foster and maintain productive working relationships with colleagues, managers, and clients.

• Exceptional communication and interpersonal skills, ideally with experience in public speaking and engaging external stakeholders.

🏝️ Benefits

• Medical, vision, and dental insurance.

• Health Savings Account (HSA).

• Flexible Spending Account (FSA).

• Employee Assistance Program (EAP).

• Life and disability insurance.

• 401(k) plan.

• Paid time off.

• Holidays.

• Parental leave.

• Bereavement leave.

• Work-life balance and flexibility.