20 publicaciones de empleo destacadas en lead medical project coordinator (¡Están contratando!)

Lead Medical Project Coordinator
Thermo Fisher Scientific —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Enfermería
- Administración de personal
- Licenciatura
7h
Senior Medical Project Coordinator
Thermo Fisher Scientific —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Enfermería
- Administración de personal
- Licenciatura
7h
Medical Project Coordinator
Thermo Fisher Scientific —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Enfermería
- Administración de personal
- Licenciatura
7h
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Baker Hughes —Ciudad de México, CDMX
- Tiempo completo
- Microsoft Excel
- Administración de personal
- Microsoft Office
- Permiso de maternidad y paternidad
- Seguro de vida
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Project Coordinator I
Fortrea —Ciudad de México, CDMX
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
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Sr. EHS & Facilities Manager
ICU Medical —Tijuana, B.C.
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Excel
- Administración de personal
Operations Project Manager III
Jabil Circuit —Guadalajara, Jal.
- Tiempo completo
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
8d
Clinical Data Coordinator
ICON Plc —Ciudad de México, CDMX
- Tiempo completo
- Oracle
- Administración de personal
- Licenciatura
- Seguro dental
- Seguro de la vista
14d
Facility Vendor & Client Services Coordinator
Touch Support —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Microsoft Excel
- Microsoft Outlook
- Inglés
Postulación rápida
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Sr. CRA with CAR-T experience to work traveling to US
Fortrea —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Administración de personal
- Inglés
- Licenciatura
Remote Executive Assistant Associate - Operations & Project Management (LATAM)
FreedUp —Ciudad de México, CDMX
- Tiempo completo
- Home Office (Desde casa)
- CRM software
Postulación rápida
Project Coordinator
Vertiv —Reynosa, Tamps.
- Correo electrónico
- Microsoft Powerpoint
- Microsoft Excel
- Oracle
VDC Coordinator
Kiewit Mexico —Querétaro, Qro.
- Administración de personal
- Inglés
- Licenciatura
- Seguro dental
- Vacaciones adicionales o permisos con goce de sueldo
Postulación rápida
Regulatory Submissions Coordinator (Biological products)
Parexel —Ciudad de México, CDMX
- Administración de personal
- Inglés
- Licenciatura
TPM Coordinator
Convatec —Del Norte, Tamps.
- Tiempo completo
- Mantenimiento
- Inglés
- Licenciatura
MEP COORDINATOR
Mucho Talento —Benito Juárez, CDMX
- Tiempo completo
- Trabajo híbrido
- Inglés
- Licenciatura
- Plomería
- Vacaciones adicionales o permisos con goce de sueldo
Postulación rápida
WHS Coordinator - 2nd-3rd Shift
Stellantis —Saltillo, Coah.
- Maestría
- Licenciatura
- Experiencia en manufactura
9d
Regional EHS Manager
Versigent —Ciudad Juárez, Chih.
- Administración de personal
- Manejo de grupos
- Liderazgo
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Médico/a internista para Misiones Humanitarias Internacionales
MEDICOS SIN FRONTERAS EN MEXICO A.C. —Ciudad de México, CDMX
- Desde $27,000 por mes
- Tiempo completo
- Microsoft Excel
- Administración de personal
- Hospital
- Seguro de vida
Postulación rápida
Tax Sr. Coordinator
Viva —Ciudad de México, CDMX
- Trabajo híbrido
- Microsoft Excel
- Administración de personal
- ERP systems
- Seguro de vida

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Lead Medical Project Coordinator

Thermo Fisher Scientific -
Desde casa

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Información del empleo

Tiempo completo
Hace 7 horas

Cualificaciones

Enfermería
Administración de personal
Licenciatura
Capacitación
Estimación y pronóstico
Negocios
Experiencia en enfermería

Descripción completa del empleo

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Lead Medical Project Coordinator

At Thermo Fisher Scientific, your work will have a meaningful impact on global health. By supporting clinical research, you'll help advance life-changing therapies while growing your career in a collaborative and innovative environment.

As a Lead Medical Project Coordinator, you'll lead the coordination and oversight of medical projects, working closely with cross-functional teams and clients to ensure high-quality delivery, effective collaboration, and successful project execution throughout the study lifecycle.

What You'll Do:

Work independently to perform and/or lead first pass review of 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. Proactively identify any potential issues and resolve or
escalate as appropriate.

Review safety data and provide comprehensive summations for safety review

meetings. Review designated sections of aggregate reports.

Initiate and lead initiatives to improve current processes and develops new

processes regarding medical monitoring and department services. May develop
guidance documents and assist with the implementation and/or revision of
corporate level documents such as SOP's and WPD's.

Independently function as the Project Lead for medical monitoring services

when SAE case processing has not been contracted. Manage project
implementation, coordination, maintenance and close out of assigned studies as
applicable. Serve as the primary point of contact for clinical project teams on
studies and can act as the alliance level lead on larger alliance/multi-protocol
studies.

Create and maintain safety and medical management plan(s) on studies (as

applicable) and ensure that the processes included in the plan document are
reflective of the contract and service requested for studies that have
department involvement as well as standalone studies (ex. MM and/or MPC).

Work independently to monitor the project financial status, unit forecasting,

actual realization, and team allocations in systems. Coordinate staff
projections based on contract values and actual hours used. Escalate any
financial and/or operational risks and can attend risk management meetings to
discuss.

Present at business development, client, and investigator meetings and

participate in strategy/business development calls. Represent studies at risk
management meetings.

Independently determine hours required for out of scope work for both the MM

and MPC and provides this to the finance/study team for contract modifications.
Attend meetings to discuss/justify the modification requirements.

Train and develop new team members. Serve as main point of contact for

team member questions with escalation to management as appropriate. May
provide input on individual performance to direct line manager. Organize and
lead meetings with team members to discuss potential process issues, answer
questions, and brainstorm ideas and solutions.

Resolve complex problems through in-depth evaluation of various factors and

offers solutions.

Education and Experience Requirements:

Bachelors degree in Nursing or related Health Sciences (Physician's Assistant) or licensed RN
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years), to include 8+ 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, Abilities:

Superior knowledge of GCPs for medical oversight of clinical trials
Advanced knowledge of drug development and safety reporting
Extensive knowledge of safety data trending to include coding
Good knowledge of biostatistics, data management and clinical procedures
Exceptional problem solving and critical thinking skills
Exceptional project management and budget skills
Excellent mentoring skills and ability to train and lead others
Exceptional oral and written communication skills
Detail-oriented mindset
Able to work in a collaborative team environment
Ability to maintain a positive and professional demeanor in challenging circumstances

Working Environment:
Thermo Fisher Scientific values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive. Below is listed the working environment/requirements for this role:

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

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.

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