6 publicaciones de empleo destacadas de medical science en buenos aires, b (¡Están contratando!)

Assoc CRA - CRA School
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
10h
FSP - Import/Export Specialist
IQVIA —Buenos Aires, Buenos Aires
- Tiempo completo
2d
Consultant - Commercial Strategy
Syneos Health Commercial Solutions —Buenos Aires, Buenos Aires
Sr. Safety Specialist
サイネオス・ヘルス —Buenos Aires, Buenos Aires
5d
Senior AWS Data Engineer
ON.energy —Capital Federal, Buenos Aires
Intern
Vylor —Buenos Aires, Buenos Aires
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FSP - Import/Export Specialist
IQVIA —Buenos Aires, Buenos Aires
At least 1 year experience related to international trade (ComEx), import and export processes in pharmaceutical industry (clinical Trials).
2d

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Assoc CRA - CRA School

IQVIA -
Buenos Aires, Buenos Aires

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Detalles del empleo

Tiempo completo
Hace 10 horas

Descripción completa del empleo

Buenos Aires, Argentina | Full time | Hybrid | R1562678

Job Overview
Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.

Essential Functions

Complete appropriate therapeutic, protocol and clinical research training to perform job duties.
Gain experience in study procedures by working with experienced clinical staff.
Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.
Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.
Under close supervision, evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution.
Under close supervision, ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) and local regulatory requirements.
Under close supervision may support start-up phase.
Under close supervision, create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Collaborate and liaise with study team members for project execution support as appropriate.
If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site recruitment progress.

Qualifications

Bachelor's Degree in scientific discipline or health care (Required)

Monitoring course completed (Pref)

Based in Buenos Aires (CABA / GBA)

Availability to travel
Written and verbal communication skills including good command of English language.

Prior clinical experience preferred.
Some organizations may require 2 years of clinical experience.
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
Organizational and problem-solving skills.
Effective time and financial management skills.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Advanced knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
Knowledge of applicable protocol requirements as provided in company training.

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

Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.

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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medical science empleos en buenos aires, b

Assoc CRA - CRA School

FSP - Import/Export Specialist

Consultant - Commercial Strategy

Sr. Safety Specialist

Senior AWS Data Engineer

Intern

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Quiero recibir la alerta de empleo más reciente para medical science en buenos aires, b

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