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

Project Associate-ideal opportunity for CTA or Project Specialist (Hybrid, Ciudad de Mexico)
サイネオス・ヘルス —Tlalnepantla, Méx.
- Inglés
- Microsoft Office
- 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
Laboratory Proj Coordinator I
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Investigación
- Seguro dental
- Seguro de la vista
Clinical Start-Up & Trial Lead (Start-Up + CTL)
Fortrea —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Licenciatura
- Disponible para viajar
Life Sciences R&D Consultant/Manager
Accenture —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Inglés
- Maestría
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 Specialist II - Mexico and Argentina - Hybrid
Syneos - Clinical and Corporate - Prod —Ciudad de México, CDMX
- Tiempo completo
- Contratos
15h
Safety & PV Specialist II - Mexico Hybrid
サイネオス・ヘルス —Tlalnepantla, Méx.
- Contratos
Logistics Manager for México, Costa Rica & El Salvador
Siemens Healthineers —Ciudad de México, CDMX
- Tiempo completo
- Trabajo híbrido
- Licenciatura
- Negocios
- Liderazgo
2d
TMF Group Lead
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Licenciatura
- Sin título de educación superior
- Seguro dental
- Seguro de la vista
16h
Operations Specialist 1
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Experiencia en bases de datos
- Licenciatura
3h
Clinical Regional Project Lead
PSI CRO —Ciudad de México, CDMX
- Tiempo completo
- Home Office (Desde casa)
- Inglés
- Microsoft Office
- Licenciatura
Postulación rápida
Clinical Scientist, Clinical Science, Cronos
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Maestría
Start-up Associate
Fortrea —Ciudad de México, CDMX
- Tiempo completo
- Licenciatura
Site Contracts Associate, Mexico, IQVIA Biotech
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Microsoft Office
- Licenciatura
Clinical Scientist in CNS - LATAM
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Inglés
- Maestría
Clinical Team Lead
Fortrea —Ciudad de México, CDMX
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Principal Statistical Programmer (Clinical Trials)
IQVIA —Ciudad de México, CDMX
- Tiempo completo
- Administración de personal
- Informática
- Inglés
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
16h

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

Al ingresar a tu cuenta, aceptas las Condiciones del servicio de SimplyHired y das tu consentimiento a nuestra Política de privacidad y Cookies.

Explorar empleos en más ubicaciones

clinical scientist, clinical science, cronos jobs near loreto cdmx

Empleos de Guest Experience & Operations en Ciudad De México

Empleos de Operations Associate en Naucalpan, Méx.

Empleos de Operations Associate en Jalisco, JAL.

Empleos de People Operations Specialist en Ciudad De México

Empleos de Operations Associate en Ciudad De México

Empleos de Project Manager en Edo. De México

Empleos de Credentialing Specialist en Ciudad De México

Empleos de Trade Compliance Specialist en Ciudad De México

Empleos de Clinical Nurse Specialist en Desde Casa

Empleos de Clinical Research en Ciudad De México

Empleos de Safety Specialist en Ciudad De México

Empleos de Hr Specialist en Tlalnepantla, Méx.

Empleos de Safety Specialist en Guadalajara, JAL.

Empleos de Cordinador Safety Mexcal en Tijuana, B.c.

Empleos de Group Leader en Celaya, GTO.

Empleos de The Destination Group en Ciudad De México

Empleos de Empleos En Mer Group en Ciudad De México

Empleos de Group Leader en El Marqués Queretano, QRO.

Empleos de Team Leader Produccion en Querétaro De Arteaga

Empleos de Gape Business Group en Ciudad De México

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

サイネオス・ヘルス
Tlalnepantla, Méx.

Postúlate ahora

Información del empleo

Cualificaciones

Inglés
Microsoft Office
Licenciatura
Contratos
Software de gestión de proyectos
Microsoft Project

Descripción completa del empleo

Updated: Yesterday
Location: Tlalnepantla, MEX, Mexico
Job ID: 25111229

Not ready to apply?
Join our Talent Network

Description

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

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

Discover what your 25,000 future colleagues already know:

Why Syneos Health

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.
We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Job Responsibilities

"JOB SUMMARY The Project Associate will drive and support overall project management activities to ensure successful execution of clinical trials, which may range from single service studies to full scope or multiple protocol and/or global projects. This role requires coordination of project tasks, maintaining documentation, communicating with stakeholders, and maintenance of timelines and budgets. A Project Associate may be allocated to function at the Sr. Project Associate (Sr. PA) level within a large project team or on a small project. JOB RESPONSIBILITIES · Drives the planning and execution of elements of clinical trials in partnership with the Project Lead. · Ensures projects adhere to strict timelines and are delivered within budget. · Coordinates internal resources and third parties/vendors for the efficient execution of projects. · Conducts ongoing analysis of project performance to drive the successful completion of short and long-term goals. · May maintain and distribute study-specific financial reports and contribute to study’s financial health using financial processes and systems. · Documents project scope and objectives, involving all relevant stakeholders. · Leads communication between project team members, ensuring all parties are informed of project status and changes. · Documents and escalates project risks and issues and drives timely follow-through and completion. · Maintenance of systems and project management tools and methodologies. · Drives quality assurance activities, including preparation for audits and internal review, prepare documentation and follow through to resolution on actionable issues. QUALIFICATION REQUIREMENTS · Bachelor’s degree (or equivalent) level of qualification in life sciences, medicine, pharmacy, nursing, project management or related field or equivalent combination of education, training and experience. · Knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory requirements. · Strong organizational skills. · Ability to manage time and work independently. · High proficiency with full MS Office Applications and/or project management software tools. · Strong communication, presentation, interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade. · Ability to travel if necessary preferred (approximately 5%). · Effective verbal and writing skills in English."

Get to know Syneos Health

Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.

No matter what your role is, you’ll take the initiative and challenge the status quo with us in a highly competitive and ever-changing environment. Learn more about Syneos Health.

http://www.syneoshealth.com

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.

Postúlate ahora

Refina tu búsqueda

clinical scientist, clinical science, cronos empleos en loreto cdmx

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

Safety & PV Specialist II - Mexico Hybrid

Data Manager for Clinical Trials

Laboratory Proj Coordinator I

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

Life Sciences R&D Consultant/Manager

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

Safety Specialist II - Mexico and Argentina - Hybrid

Safety & PV Specialist II - Mexico Hybrid

Logistics Manager for México, Costa Rica & El Salvador

TMF Group Lead

Operations Specialist 1

Clinical Regional Project Lead

Clinical Scientist, Clinical Science, Cronos

Start-up Associate

Site Contracts Associate, Mexico, IQVIA Biotech

Clinical Scientist in CNS - LATAM

Clinical Team Lead

Principal Statistical Programmer (Clinical Trials)

Site Specialist II

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

Related Searches

Explorar empleos en más ubicaciones

Herramientas para candidatos

Herramientas para empresas

Explorar

Mantente conectado