Remote Bilingual Medical Front Desk Coordinator

Entrepreneur Cooperative; Ciudad de Mendoza; Remote; ARS 232,274,000 - 325,183,000; Full time

Job summary

IQVIA is seeking an Associate Medical Director / Medical Director - Dermatology to provide medical, clinical, and scientific advisory expertise across divisions. The role involves serving as a Global Medical Advisor on projects, guiding project leaders on medical aspects, and ensuring patient safety and protocol integrity throughout the trial lifecycle.

Required qualifications include an MD with Dermatology board certification, 5+ years in clinical medicine, and 4+ years in clinical trials.

Qualifications

• Excellent communication, presentation and interpersonal skills, including command of English (written and spoken).
• Certification in Dermatology is mandatory and Specialty Board certification required.
• At least 5 years of experience in clinical medicine in addition to 4 years of clinical trials experience as an investigator or in Pharma/CRO/Biotech.

Responsibilities

• Provide medical, clinical and scientific advisory expertise to all IQVIA divisions.
• Serve as Global Medical Advisor on assigned projects and support project teams.
• Review protocol documents, IDB/CRFs, and adverse events with safety focus.
• Ensure medical oversight during Investigator Meetings and trial delivery lifecycle.
• Coordinate with Pharmacovigilance for SAEs and other safety reviews.

Skills

English language

Clinical trials experience

Education

Medical degree

Dermatology board certification

Job description

Buenos Aires, Argentina Mexican City, Mexico São Paulo, Brazil Full time R **Job Overview** The Associate Medical Director / Medical Director - **Dermatology** will provide medical, clinical and scientific advisory expertise to all IQVIA divisions as requested; participate in all aspects of Medical Science involvement on assigned trials; serve as a medical expert during project delivery lifecycle; provide therapeutic and medical expertise to business development activities. **Essential Functions** - Primarily serves as **Global Medical Advisor** on assigned projects. - Serves as **Scientific Advisor** and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects. - Provides medical support to investigative sites and project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility. - Performs medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs). - Performs review and clarification of trial-related Adverse Events (AEs). - Provides therapeutic area/indication training for the project clinical team. - Attends and presents at Investigator Meetings. - May perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department. - May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department. - May perform medical review of adverse event coding. - Performs review of the Clinical Study Report (CSR) and patient narratives. - Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested. **Requirements** - May require regular travel. - Extensive use of keyboard requiring repetitive motion of fingers. - Extensive use of telephone and face-to-face communication requiring accurate perception of speech. **Qualifications** - Excellent communication, presentation and interpersonal skills, including the command of **English** language (both written and spoken). - **Medical degree** from an accredited and internationally recognized medical school with a curriculum relevant to general medical education. - Certification in **Dermatology** (mandatory) - **Specialty Board certification required** . - At least 5 years of experience in clinical medicine in addition to **4 years of clinical trials experience** as an investigator or in the Pharma, CRO, or Biotech industry. - Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in applicable therapeutic area. - Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research. - Excellent skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility. EEObottom