10 дней назад
Associate Medical Director - Dermatology
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Associate Medical Director - Dermatology (Clinical Trials): Providing medical, clinical, and scientific advisory expertise for dermatology clinical trials with an accent on protocol review, patient safety, and investigator support. Focus on reviewing adverse events and clinical study reports, advising project teams, and presenting therapeutic-area guidance during trial delivery.
Location: Buenos Aires, Argentina
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Serve as a global medical and scientific advisor on assigned dermatology clinical trial projects.
- Provide medical guidance to project leaders, investigative sites, and project staff on protocol clarifications, eligibility, and patient safety.
- Review protocols, Investigative Drug Brochures, Case Report Forms, adverse events, clinical study reports, and patient narratives.
- Support Serious Adverse Event reviews, Analysis of Similar Events, and adverse event coding in collaboration with Pharmacovigilance.
- Deliver therapeutic-area training and present at investigator, kick-off, team, and client meetings.
- Provide medical and therapeutic expertise for business development activities and project delivery.
Requirements
- Medical degree from an accredited and internationally recognized medical school.
- Mandatory Dermatology certification and specialty board certification.
- At least five years of clinical medicine experience and four years of clinical trials experience as an investigator or in the pharmaceutical, CRO, or biotech industry.
- Excellent written and spoken English communication, presentation, and interpersonal skills.
- Current knowledge of the scientific, clinical, regulatory, commercial, and competitive landscape in dermatology.
- Availability 24 hours a day, 7 days a week to respond to urgent protocol-related issues; regular travel may be required.
Culture & Benefits
- Full-time position supporting global clinical research and medical development programs.
- Regular collaboration with project leaders, investigative sites, Pharmacovigilance, clients, and clinical teams.
- Participation in investigator meetings, kick-off meetings, weekly team meetings, and client meetings.
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