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

Start-up Associate
Fortrea —Ciudad de México, CDMX
- Tiempo completo
- Licenciatura
Safety & PV Specialist II - Mexico Hybrid
Syneos - Clinical and Corporate - Prod —Ciudad de México, CDMX
- Tiempo completo
- Contratos
Data Manager for Clinical Trials
PSI CRO —Ciudad de México, CDMX
- Tiempo completo
- Home Office (Desde casa)
- Oracle
- Administración de personal
- Inglés
Postulación rápida
Clinical Scientist, Clinical Science, Cronos
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Maestría
Clinical Scientist in CNS - LATAM
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Maestría
Lead Specialist, Healthcare Market Access & Reimbursement (LAM) - Mexico or Colombia
Siemens Healthineers —Ciudad de México, CDMX
- Tiempo completo
- Trabajo híbrido
- Administración de personal
- Inglés
- Maestría
11d
Clinical Team Lead
Fortrea —Ciudad de México, CDMX
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Logistics Manager for México, Costa Rica & El Salvador
Siemens Healthineers —Ciudad de México, CDMX
- Tiempo completo
- Trabajo híbrido
- Licenciatura
- Negocios
- Liderazgo
4d
Clinical Regional Project Lead
PSI CRO —Ciudad de México, CDMX
- Tiempo completo
- Home Office (Desde casa)
- Inglés
- Microsoft Office
- Licenciatura
Postulación rápida
Site Contracts Associate, Mexico, IQVIA Biotech
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Microsoft Office
- Licenciatura
Clinical Trial Investigator Grant Forecasting
Fortrea —Ciudad de México, CDMX
- Tiempo completo
- Microsoft Excel
- Administración de personal
- ERP systems
14d
Principal Statistical Programmer (Clinical Trials)
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Informática
- Inglés
Operations Specialist 1
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Experiencia en bases de datos
- Licenciatura
1d
Bilingual 3Shape Specialist Designer.
Solventum —Ciudad de México, CDMX
- Tiempo completo
- Bilingüe
- Inglés
Centralized Monitoring Lead in LATAM (Remote)
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Home Office (Desde casa)
- Inglés
- Licenciatura
Sr Clinical Trial Manager - Global Studies
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Investigación
- Licenciatura
Safety Specialist II - Mexico and Argentina - Hybrid
Syneos - Clinical and Corporate - Prod —Ciudad de México, CDMX
- Tiempo completo
- Contratos
2d
Representante médico virtual: Col. Nápoles.
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Licenciatura
Central Monitor in LATAM
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Enfermería
- Microsoft Excel
- Inglés
Sr Clin Data Assoc
Thermo Fisher Scientific —Ampliación Nápoles, CDMX
- Tiempo completo
- Enfermería
- Oracle
- Administración de personal

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Start-up Associate

Fortrea -
Ciudad de México, CDMX

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Información del empleo

Tiempo completo

Cualificaciones

Licenciatura

Descripción completa del empleo

Job Overview:

Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within the timelines agreed with project management and Site Readiness team. Develop awareness of regulatory legislation, guidance, and practice in the assigned countries with the support from senior staff.

Summary of Responsibilities:

Develop awareness of regulatory legislation, guidance, and practice in the assigned countries with the support from senior staff.
Assist senior staff to compile, prepare, submit, and obtain approval of the submission documents to IRB/IEC/Third body/Regulatory Authority in accordance with local requirements.
Liaise with internal and external vendors in the generation of Regulatory Authority submissions (as applicable).
Perform a review of final submission documents as applicable.
Organize communication related to the submissions/outcomes within Fortrea as applicable.
Escalate study issues appropriately and in a timely fashion.
Perform other duties as assigned by management depending upon country and situational requirements with proper supervision (if applicable).
In Country specific tasks (Global):
Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner.
Collect and track all the necessary documents required and perform a quality review, formatting, and compilation of the final documents for effective and compliant site activation and maintenance.
Ensure that all assigned maintenance and Start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality and applicable laws and guidelines.
Update study documents when there are changes in study personnel/study amendments.
Ensure high quality documents are filed and systems are updated on an ongoing and timely basis, making Fortrea ready for an audit at any time.
Update status reports, applicable logs, and tracking systems as applicable for the projects with input provided by senior staff.
With guidance from line manager and experienced colleagues, adapt Informed Consent Forms and other patient facing material to country specific requirements.
May support / assist the contract negotiation process under supervision of an experienced colleague or line manager.
Proactively identifying and escalating to Submission Leads any risk to meeting deliverables.
Notify the Submissions Lead of hours identified as Out-of-Scope or over burn with the support of more senior specialists.
All other duties as needed or assigned.
Clinical Trials Information System (CTIS) tasks (specific centralized role for EU):
Upload of submission documentation to CTIS under supervision as applicable.

Qualifications (Minimum Required):

University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology).
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Experience (Minimum Required):

Minimum 0 – 2 + years of experience, or an equivalent combination of education and experience to successfully perform the key responsibilities of the job.
Working knowledge of ICH, RA, IRB/IEC, and other applicable regulations/guidelines
Demonstrated basic understanding of the clinical trial process.

Physical Demands/Work Environment:

General Office Environment.

Learn more about our EEO & Accommodations request here .

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Refina tu búsqueda

clinical scientist, clinical science, empleos en loreto cdmx

Start-up Associate

Safety & PV Specialist II - Mexico Hybrid

Data Manager for Clinical Trials

Clinical Scientist, Clinical Science, Cronos

Clinical Scientist in CNS - LATAM

Lead Specialist, Healthcare Market Access & Reimbursement (LAM) - Mexico or Colombia

Clinical Team Lead

Logistics Manager for México, Costa Rica & El Salvador

Clinical Regional Project Lead

Site Contracts Associate, Mexico, IQVIA Biotech

Clinical Trial Investigator Grant Forecasting

Principal Statistical Programmer (Clinical Trials)

Operations Specialist 1

Bilingual 3Shape Specialist Designer.

Centralized Monitoring Lead in LATAM (Remote)

Sr Clinical Trial Manager - Global Studies

Safety Specialist II - Mexico and Argentina - Hybrid

Representante médico virtual: Col. Nápoles.

Central Monitor in LATAM

Sr Clin Data Assoc

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

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