20 publicaciones de empleo destacadas de clinical scientist, clinical science, en loreto cdmx (¡Están contratando!)

Clinical Trial Psych Rater - US Spanish Speaking
IQVIA —Ciudad de México, CDMX
- $62,700 a $156,700 por año
- Medio tiempo
- Administración de personal
- Doctorado
- Inglés
Laboratory Proj Coordinator I
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Investigación
- Seguro dental
- Seguro de la vista
Clinical Lead - Global Study Leadership
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Licenciatura
- Mejora continua
Clinical Data Science Programmer
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Oracle
- Informática
- Inglés
- Seguro dental
- Seguro de la vista
12d
Centralized Monitoring Lead in LATAM (Remote)
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Home Office (Desde casa)
- Inglés
- Licenciatura
Site Management Associate
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Licenciatura
- Disponible para viajar
- Seguro dental
- Seguro de la vista
8h
Project Associate-ideal opportunity for CTA or Project Specialist (Hybrid, Ciudad de Mexico)
Syneos - Clinical and Corporate - Prod —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Microsoft Office
- Licenciatura
Safety & PV Specialist II - Mexico Hybrid
サイネオス・ヘルス —Tlalnepantla, Méx.
- Contratos
Clinical Scientist, Clinical Science, Cronos
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Maestría
Drug Safety Physician
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Licenciatura
- Seguro dental
- Seguro de la vista
Analyst (Consulting)
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Maestría
- Licenciatura
Central Monitor in LATAM
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Enfermería
- Microsoft Excel
- Inglés
Clinical Start-Up & Trial Lead (Start-Up + CTL)
Fortrea —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Licenciatura
- Disponible para viajar
Site Contracts Associate, Mexico, IQVIA Biotech
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Microsoft Office
- Licenciatura
Lead Specialist, Healthcare Market Access & Reimbursement (LAM)
Siemens Healthineers —Ciudad de México, CDMX
- Tiempo completo
- Trabajo híbrido
- Administración de personal
- Inglés
- Maestría
9d
Lead Clinical Research Associate
PSI CRO —Ciudad de México, CDMX
- Tiempo completo
- Home Office (Desde casa)
- Inglés
- Microsoft Office
- Licenciatura
Postulación rápida
Consulting Intern
IQVIA —Ciudad de México, CDMX
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Sr Clinical Trial Manager - Global Studies
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Investigación
- Licenciatura
Site Specialist II
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Licenciatura
- Sin título de educación superior
- Habilidades de organización
- Seguro dental
- Seguro de la vista
8h
Sr. CRA - Mexico (FSP - Sponsor Dedicated)
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Enfermería
- Administración de personal
- Disponible para viajar
- Seguro dental
- Seguro de la vista

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Clinical Trial Psych Rater - US Spanish Speaking

IQVIA -
Ciudad de México, CDMX

Postúlate ahora

Información del empleo

Medio tiempo
$62,700 a $156,700 por año

Cualificaciones

Administración de personal
Doctorado
Inglés
Microsoft Office
Maestría
Habilidades de comunicación
Administración del tiempo

Descripción completa del empleo

Mexico City, Mexico | Part time | Home-based | R1563625

Clinical Trial Psych Rater - US Spanish Speaking

Location: Remote/Virtual
Hours: Estimated 10–16 hours per month
Role: Clinical Specialist

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.

Position Overview

The Clinical Specialist plays a key role in ensuring the integrity and reliability of clinical trial data. This position involves reviewing scales administered by raters to confirm standardized assessment practices. Responsibilities include evaluating assessment quality, engaging in live discussions with raters to provide guidance on methodology and scoring techniques, and supporting rater performance through functional assessments (e.g., mock interviews). Additional tasks may include assisting with communication materials and documentation.

Key Responsibilities

Participate in all required orientation, training, and calibration activities.
Review case data and prepare for rater discussions, ensuring all relevant documents and scale items are available.
Conduct live interactions with raters to provide feedback and guidance on assessment methodology and scoring.
Complete assigned tasks and rater interactions according to schedule.
Submit all required documentation accurately and on time.

Required Qualifications

Education: Master’s degree (MA/MS) in Psychology, Counseling, Psychiatric Nursing, or Social Work (or equivalent). MD, DO, or PhD preferred.
Experience:
- Minimum 3 years administering psychiatric assessments, rating scales, and/or structured clinical interviews (specifically PANSS, MINI and CGI-SCH).
- Minimum 3 years of clinical experience with psychiatric populations.
- Minimum 3 years administering scales in clinical research trials (excluding graduate/doctoral research).
- Experience in CNS trials preferred.
Skills:
- Strong interpersonal and communication skills for professional interaction at all levels.
- Excellent organizational skills, attention to detail, time management, and problem-solving ability.
- Proficiency with Windows and Microsoft Office applications.

Language Requirement

Current openings require fluency in English and native-level proficiency in US Spanish.

#LI-DNP #LI-Remote #LI-HCPN

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 proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

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.

The potential base pay range for this role, when annualized, is $62,700.00 - $156,700.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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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Refina tu búsqueda

clinical scientist, clinical science, empleos en loreto cdmx

Clinical Trial Psych Rater - US Spanish Speaking

Laboratory Proj Coordinator I

Clinical Lead - Global Study Leadership

Clinical Data Science Programmer

Centralized Monitoring Lead in LATAM (Remote)

Site Management Associate

Project Associate-ideal opportunity for CTA or Project Specialist (Hybrid, Ciudad de Mexico)

Safety & PV Specialist II - Mexico Hybrid

Clinical Scientist, Clinical Science, Cronos

Drug Safety Physician

Analyst (Consulting)

Central Monitor in LATAM

Clinical Start-Up & Trial Lead (Start-Up + CTL)

Site Contracts Associate, Mexico, IQVIA Biotech

Lead Specialist, Healthcare Market Access & Reimbursement (LAM)

Lead Clinical Research Associate

Consulting Intern

Sr Clinical Trial Manager - Global Studies

Site Specialist II

Sr. CRA - Mexico (FSP - Sponsor Dedicated)

Quiero recibir la alerta de empleo más reciente para clinical scientist, clinical science, en loreto cdmx

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