14 publicaciones de empleo destacadas de science lead en desde casa (¡Están contratando!)

Senior CRA level I
Thermo Fisher Scientific —Desde casa
- Tiempo completo
- Enfermería
- Administración de personal
- Inglés
Lead Medical Project Coordinator
Thermo Fisher Scientific —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Enfermería
- Administración de personal
- Licenciatura
Medical Project Coordinator
Thermo Fisher Scientific —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Enfermería
- Administración de personal
- Licenciatura
Patient Engagement Lead (LATAM)
Precision Medicine Group —Desde casa
- Home Office (Desde casa)
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Account Manager
Julius 2 Grow —Desde casa
- $20,000 a $35,000 por mes
- Tiempo completo
- Home Office (Desde casa)
- Administración de personal
- Mercadotecnia
- Inglés
Postulación rápida
11d
Sales Development Representative (Contract, Remote, LATAM - Life Sciences)
LARVOL —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Experiencia en ventas
- Salesforce
- Inglés
Postulación rápida
11d
Senior Clinical Data Engineer (LATAM)
Precision for Medicine —Desde casa
- Home Office (Desde casa)
- Administración de personal
- Inglés
- SQL
Postulación rápida
Senior Software Engineer - JAVA (Level V)
Confiz —Desde casa
- Home Office (Desde casa)
- DevOps
- Java
- Experiencia en bases de datos
Postulación rápida
Senior Database Reliability Engineer
Sezzle —Desde casa
- $5,000 a $9,500 por mes
- Tiempo completo
- Home Office (Desde casa)
- Administración de personal
- Informática
- DevOps
Manager Cloud, DevOps Engineering
Solera —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Azure
- Informática
- DevOps
Java Engineer Level III - AWS , Kafka, Kubernetes (MEXICO ONLY)
Confiz —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Informática
- Java
- Maestría
Postulación rápida
Senior Engineer- Generative AI & ML
Confiz —Desde casa
- Home Office (Desde casa)
- Informática
- Maestría
- Licenciatura
Postulación rápida
Senior Solution Consultant
Trellix —Desde casa
- Home Office (Desde casa)
- Azure
- Administración de personal
- Experiencia en bases de datos
- Seguro dental
- Vacaciones adicionales o permisos con goce de sueldo
Senior Cloud Architect, Delivery (GenAI)
DoiT —Desde casa
- Tiempo completo
- Home Office (Desde casa)
- Azure
- Informática
- DevOps
- Permiso de maternidad y paternidad
Postulación rápida

More jobs to discover

Find similar jobs that you might be interested in.

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…
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…

Quiero recibir la alerta de empleo más reciente para science lead en desde casa

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

science lead jobs near desde casa

Empleos de Senior Ai Ml Engineer en Desde Casa

Empleos de Account Manager en Desde Casa

Empleos de Sitel Mexico Services, S A De en Iztapalapa, CDMX

Empleos de Fermaca Services en Ciudad De México

Empleos de Piston Trucks Prologic Services en Atizapán De Zaragoza, Méx.

Empleos de Sap Consultant en Ciudad De México

Empleos de Science Teacher en San Mateo Xalpa, CDMX

Empleos de Data Science en Toluca, Méx.

Empleos de Project Coordinator en Puebla

Empleos de Project Coordinator en Ciudad De México

Empleos de Project Manager en Zapopan, JAL.

Empleos de Project Manager en Guadalajara, JAL.

Empleos de Project Coordinator en Monterrey, N. L.

Empleos de Project Coordinator en Renovación, CDMX

Empleos de Project Coordinator en Jalisco

Empleos de Scrum Master Project Manager en Ciudad De México

Empleos de Project Manager Construction en Ciudad De México

Empleos de Chemical Engineer en Ciudad De México

Empleos de Research Analyst en Ciudad De México

Empleos de 100 Market Research en Ciudad De México

Senior CRA level I

Thermo Fisher Scientific -
Desde casa

Postúlate ahora

Información del empleo

Tiempo completo

Cualificaciones

Enfermería
Administración de personal
Inglés
Microsoft Office
Licenciatura
Uso de computadora
Terminología médica
Administración del tiempo

Descripción completa del empleo

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Senior Clinical Research Associate (Level I) – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Senior Clinical Research Associate (Level I), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You’ll Do:

Monitors investigator sites with a risk-based monitoring approach: applies rootcause analysis (RCA), critical thinking and problem-solving skills to identify siteprocesses failure and corrective/preventive actions to bring the site intocompliance and decrease risks. Ensures data accuracy through SDR, SDV andCRF review as applicable through on-site and remote monitoring activities.Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System, CTMS). Performs QC check of reports generated from CTMS system where required.
Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Ensures trial close out and retrieval of trial materials.
Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
Contributes to the project team by assisting in preparation of project publications/tools, and sharing ideas/suggestions with team members. Performs additional study tasks as assigned by CTM (e.g. trip report review, newsletter creation, lead CRA team calls etc).
Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:

Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 2+ years as a clinical research monitor).
Valid driver's license where applicable
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:

Effective clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Excellent understanding and demonstrated application of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
Ability to manages Risk Based Monitoring concepts and processes
Effective oral and written communication skills, with the ability to communicate effectively with medical personnel
Ability to maintain customer focus through the utilization of good listening skills, attention to detailand the ability to perceive customers’ underlying issues
Effective interpersonal skills
Strong attention to detail
Effective organizational and time management skills
Ability to remain flexible and adaptable in a wide range of scenarios
Ability to work in a team or independently as required
Good computer skills: proficient knowledge of Microsoft Office and the ability to learn appropriate software
Good English language and grammar skills
Good presentation skills

Working Conditions and Environment:

Working Conditions and Environment:
Work is performed in an office/ laboratory/clinical/and/or home office environment with exposure to electrical office equipment.
Frequent drives to site locations. Frequent travel, generally 60-80% but more for some individuals.
May also include extended overnight stays.
Exposure to biological fluids with potential exposure to infectious organisms.
Personal protective equipment required such as protective eyewear, garments and gloves.
Exposure to fluctuating and/or extreme temperatures on rare occasions.
Must be able to comply with specific sponsor/client/site requirements, even if not required by Thermo Fisher Scientific (e.g., disclosure of vaccination status, or other personal information). On some occasions, this information may be required to be provided directly to sponsor/client/site.

Postúlate ahora

Refina tu búsqueda

science lead empleos en desde casa

Senior CRA level I

Lead Medical Project Coordinator

Medical Project Coordinator

Patient Engagement Lead (LATAM)

Account Manager

Sales Development Representative (Contract, Remote, LATAM - Life Sciences)

Senior Clinical Data Engineer (LATAM)

Senior Software Engineer - JAVA (Level V)

Senior Database Reliability Engineer

Manager Cloud, DevOps Engineering

Java Engineer Level III - AWS , Kafka, Kubernetes (MEXICO ONLY)

Senior Engineer- Generative AI & ML

Senior Solution Consultant

Senior Cloud Architect, Delivery (GenAI)

More jobs to discover

Quiero recibir la alerta de empleo más reciente para science lead en desde casa

Related Searches

Explorar empleos en más ubicaciones

Herramientas para candidatos

Herramientas para empresas

Explorar

Mantente conectado