Associate Medical Director- Neurology

IQVIA; Madrid; Presencial; EUR 120.000 - 180.000; Jornada completa

Descripción de la vacante

IQVIA is seeking an Associate Medical Director / Medical Director to provide medical, clinical, and scientific advisory support across divisions. You will contribute to Medical Monitoring and Medical Strategy activities, review protocols and reports, and assist with business development through medical insight.

The role requires a medical degree, neurology certification, and clinical trials experience, with strong English communication and global collaboration skills.

Formación

• Medical degree from an accredited medical school.
• Neurology board certification is required.
• Ideally 2+ years of clinical trials experience as investigator or medical expert.
• Strong communication and interpersonal skills in English.
• Ability to provide medical and scientific guidance to multi-region teams.

Responsabilidades

• Act as Global/Regional Medical Advisor on assigned projects.
• Provide medical monitoring and scientific input to project leaders.
• Review protocols, IDB/CRFs, and CSR with medical accuracy.
• Deliver medical training and clarify adverse events with sites and teams.
• Travel regionally or internationally as required.

Conocimientos

Clinical trials experience

English communication

Stakeholder management

Educación

Medical degree

Neurology board certification

Descripción del empleo

Job Overview

The Associate Medical Director / Medical Director 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

The role includes predominantly Medical Monitoring responsibilities with Medical Strategic input involvement as requested.

Medical Monitoring

• – Primarily serves as Global and /or Regional 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).
• – Provides therapeutic area/indication training for the project clinical team.
• – Attends and presents at Investigator Meetings.
• – Performs review and clarification of trial-related Adverse Events (AEs).
• – 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.
• – Available 24/7 to respond urgent protocol -related questions from investigative sites, in accordance with local labor laws.

Medical Strategy

• – Provides expert advises to the development of medically sounded delivery strategies for small to large and/or complex multi-region studies in partnership with sales and other functions responsible for business development activities.
• – Responsible for the development of the medically related aspects of client proposals including the budget related to medical monitoring.
• – Provides medical and scientific advises to key internal stakeholders developing proposals: this may include, but is not limited to, reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
• – Attends and presents at bid defense meeting, as required.
• – Participates in strategic business development activities including presentations to prospective clients.
• – Maintains awareness of industry development and may author related publications.
• – Requires periodic regional and international travel.

Qualifications

• – Medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education, plus a minimum of 5 years’ experience in clinical medicine.
• – Specialty board certification- Neurology
• – Ideally, candidate will have a minimum 2 years clinical trials experience as an investigator or medical /clinical expert in the Pharma, CRO, or Biotech industry.
• – Ability to establish and maintain effective working relationships with co-workers, managers and clients.
• – Strong communication, presentation and interpersonal skills, including good command of English language (both written and spoken).
• – Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in applicable therapeutic area.
• – Proven skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility.

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.