12 publicaciones de empleo destacadas de coordinator, gss collections en argentina (¡Están contratando!)

Medical Project Coordinator
Thermo Fisher Scientific —Desde casa
- Tiempo completo
2h
Lead Medical Project Coordinator
Thermo Fisher Scientific —Desde casa
- Tiempo completo
2h
Pasito (YC S22) - Business Operations Associate
Silver.dev —Buenos Aires, Buenos Aires
- Tiempo completo
10h
Quality Assurance Analyst
Givaudan —Munro, Buenos Aires
13d
Call Center Agent, 6 month FTC. Fluency in German and English essential
サイネオス・ヘルス —Buenos Aires, Buenos Aires
Clinical Reseach Associate I
ICON Plc —Buenos Aires, Buenos Aires
- Tiempo completo
Paid Media Specialist
Latino Legends —Buenos Aires, Buenos Aires
Postulación rápida
Clinical Data Associate III / Sr CDA (FSP) - Min 2 years of previous data management exp - Argentina, home-based
サイネオス・ヘルス —Buenos Aires, Buenos Aires
6d
Sr CRA I
Fortrea —Buenos Aires, Buenos Aires
- Tiempo completo
Material Handler I
Thermo Fisher Scientific —Buenos Aires, Buenos Aires
- Tiempo completo
1d
Clinical Supply Chain Manager ** open to several EMEA & LATAM countries (Homebased) **
サイネオス・ヘルス —Buenos Aires, Buenos Aires
8d
Senior Medical Project Coordinator
Thermo Fisher Scientific —Desde casa
- Tiempo completo
2h

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Lead Medical Project Coordinator
Thermo Fisher Scientific —Desde casa
As a Lead Medical Project Coordinator, you'll lead the coordination and oversight of medical projects, working closely with cross-functional teams and clients…
2h
Medical Project Coordinator
Thermo Fisher Scientific —Desde casa
Knowledge of GCPs for medical oversight of clinical trials and SAE processing. May serve as the primary point of contact for clinical/data management project…
2h

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Medical Project Coordinator

Thermo Fisher Scientific -
Desde casa

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Detalles del empleo

Tiempo completo
Hace 2 horas

Descripción completa del empleo

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join us as Medical Project Coordinator – And utilize your expertise to support and enhance drug safety operations, ensuring compliance with regulatory standards and optimal patient safety in clinical trials.

What You’ll Do:

Coordinate and review safety data, utilizing line listings, company dashboard(s) and/or other visualization tools. Review data for safety trends,

coding consistencies, and potential follow up with investigator sites. Identify potential issues and resolve or escalate as appropriate.

Review safety data and may provide summations for safety review meetings.
May review designated sections of aggregate reports.
May help to create/review safety and medical management plan(s) on studies (as applicable) and ensures that the processes included in plan documents are reflective of the contract and services requested.
May help manage routine project implementation, forecasting and coordination, including review of metrics and budget considerations.
Monitor the status of the data review and escalate any delays and/or risks to all stakeholders, including study leads.
May present at business development, client, and investigator meetings and participate in strategy/business development calls.
Resolve complex problems through in-depth evaluation of various factors and offers solutions.
May serve as the primary point of contact for clinical/data management project teams.
May assist management in training and mentoring.

Education and Experience:

Bachelor’s degree in nursing or related Health Sciences (Physician's Assistant) or licensed RN
Previous experience to provide the knowledge, skills, and abilities to perform the job (comparable to 2+ years), to include 2+ years clinical safety experience (clinical research monitoring, or pharmacovigilance or combination of clinical research monitoring and pharmacovigilance)

In some cases, an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills and Abilities:

Knowledge of GCPs for medical oversight of clinical trials and SAE processing
Knowledge of drug development and safety reporting
Knowledge of safety data trending to include coding
Working knowledge of biostatistics, data management and clinical procedures
Strong problem solving and critical thinking skills
Good oral and written communication skills
Good attention to detail
Ability to work in a collaborative team environment
Ability to maintain a positive and professional demeanor in challenging circumstances

Working Conditions and Environment:

Work is performed in an office/ laboratory and/or a clinical environment.
Exposure to biological fluids with potential exposure to infectious organisms.
Exposure to electrical office equipment.
Personal protective equipment required such as protective eyewear, garments and gloves.

Physical Requirements:

Ability to work in an upright and /or stationary position for 6-8 hours per day.
Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.
Frequent mobility required.
Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf.
Ability to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
Frequently interacts with others to obtain or relate information to diverse groups.
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multitask.
Regular and consistent attendance.

Why Join Us?
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.

Apply today to help us deliver tomorrow’s breakthrough.

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coordinator, gss collections empleos en argentina

Medical Project Coordinator

Lead Medical Project Coordinator

Pasito (YC S22) - Business Operations Associate

Quality Assurance Analyst

Call Center Agent, 6 month FTC. Fluency in German and English essential

Clinical Reseach Associate I

Paid Media Specialist

Clinical Data Associate III / Sr CDA (FSP) - Min 2 years of previous data management exp - Argentina, home-based

Sr CRA I

Material Handler I

Clinical Supply Chain Manager open to several EMEA & LATAM countries (Homebased)

Senior Medical Project Coordinator

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