20 publicaciones de empleo destacadas de medical science en palermo buenos aires (¡Están contratando!)

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- Tiempo completo
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IQVIA —Buenos Aires, Buenos Aires
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IQVIA —Buenos Aires, Buenos Aires
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IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
Sr Clinical Project Manager
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
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CRA1
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
Sr Clinical Trial Manager - Global Studies
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
Centralized Monitoring Lead in LATAM (Remote)
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo

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Senior Medical Data and Safety Review Physician

IQVIA -
Buenos Aires, Buenos Aires

Postulate ahora

Detalles del empleo

Tiempo completo
Hace 9 horas

Descripción completa del empleo

Buenos Aires, Argentina | Full time | Home-based | R1562907

JOB SUMMARY:

Responsible for medical data review and medical safety case processing and related safety activities. Performs review of medical data to ensure medical/scientific plausibility and to employ medical assessment and knowledge. Also, provides medical expertise in assigned trials and standalone safety projects. Train and mentor team members in medical and safety review activities.

ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES:

Attend and present Medical Data Review activities during the client Kick Off Meeting.
Write Medical Data Review Plan in collaboration with the Medical Monitor and in accordance with the client input.
Create protocol specific Medical Data Review Guide in collaboration with the Medical Monitor.
Participate in the internal eCRF review meeting and contribute to the development of eCRF.
Define data capture requirements as required throughout the study that are consistent with the protocol and reporting needs.
Contribute to the Data Review Plan.
Provide requirements and specifications for programming of data listings.
Collaborate with Clinical Science and Data Operations teams in the development of Qlik Sense builds and protocol specific customizations for patient profiles.
Participate in activities involving risk assessment and measuring the effectiveness of risk minimization measures.
Provide medical review of data listings and patient profiles, including but not limited to, adverse events, concomitant medications, medical history, labs, vitals, ECGs, eligibility criteria, efficacy assessments and study specific assessments.
Prepare protocol specific templates for the periodic summary reports for safety data, including the Safety Trend Analysis Report (STAR) or Safety Review Committee slide presentations, in collaboration with the Medical Monitor.
Compose the STAR report during the study according to scope and timelines.
Conduct in-stream data trend analysis in support of data quality and integrity including protocol compliance and targeted review of patient data.
Prepare periodic MDR summary reports or presentations if requested.
Medical review and case assessment of SAEs including assessment and coding of preferred term, medical history, indications of concomitant medications and treatment medications; determination of seriousness, causality, expectedness; narrative review; query generation and follow up of SAE till case closure.
Compose sponsor comment/summary.
Compose, edit, and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements.

MINIMUM REQUIRED EDUCATION AND EXPERIENCE:

Medical degree from an accredited, internationally recognized medical school.
Recipient of a medical license from the country or region in which he/she currently resides or previously resided.
5 years of experience in the practice of medicine in a clinical or academic setting which may include specialty medical training or fellowship.
Minimum of 3 years of experience in Medical Data Review and/or Medical Safety Review.
Advanced English level.
Knowledge of MedRA, WhoDrug.
Previous experience in Medidata Rave, Inform.
Previous experience in Argus Safety.
Solid experience with Excel, Power Point and other data visualization tools as Spotfire, J Review, others.
Availability to work in a flexible global schedule.

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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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