Remote Bilingual Medical Front Desk Coordinator

Entrepreneur Cooperative

Buenos Aires

Remote

ARS 278,728,000 - 371,638,000

Full time

3 days ago
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Job summary

IQVIA is seeking an Associate Medical Director in Dermatology to provide medical, clinical, and scientific advisory support across divisions. The role involves serving as a global medical advisor on projects and guiding leaders on medical and scientific aspects.

The candidate should have a medical degree with dermatology certification and at least 5 years of clinical medicine experience plus 4 years in clinical trials within pharma/CRO/biotech.

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.

Responsibilities

  • Provide medical, clinical and scientific advisory expertise to IQVIA divisions.
  • Serve as Global Medical Advisor on assigned projects and provide guidance to Project Leaders on medical and scientific aspects.
  • Support investigative sites and project staff for protocol-related issues including safety and eligibility.
  • Review protocols, IDBs, CRFs and adverse events; provide medical interpretation as needed.
  • Train on therapeutic area indications for project teams and participate in investigator meetings.
  • May review SAEs and patient narratives in collaboration with Pharmacovigilance.
  • Contribute to AOSE analyses and adverse event coding review as needed.
  • Participate in CSR review and patient narratives; attend kickoff and client meetings.

Skills

Excellent communication skills
English proficiency (written and oral)

Education

Medical degree

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

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