Job summary the sr. scientist drug safety will perform in line medical safety review of individual case safety reports (icsrs) reports and other ae reports of interest: as required per sop and in conjunction with the icmr physician/management and/or therapeutic area team lead performs adverse experience reports review from specified sources in the safety database for regulatory reporting purposes apply knowledge of safety profiles for the adverse experience reports review develop working knowledge of pharmacovilance and regulatory reporting of icsrs consult with the icmr physician/management and/or therapeutic area team lead for cases requiring additional clinical or safety subject matter expertise may perform medical review of other reports of adverse events as required in conjunction with the icmr physician/management and/or therapeutic area team lead may perform icsr follow up activities in conjunction with the icmr physician/management and/or therapeutic area team lead may participate in process, quality, innovation, technology and other business-related activities under the guidance of icmr physician/management may participate on special projects or rotational assignments within or outside of icmr the icmr associate with oversight from the icmr physician/management and/or therapeutic area team lead, may work closely and collaboratively with colleagues in other departments in the company, including but not limited to: global and us pharmacovigilance, global pharmacovigilance case management, and clinical safety & risk management. education: - advanced/gradua...
Job summary job description current employees apply here current contingent workers apply here search firm representatives please read carefully merck & co. inc. rahway nj usa also known as merck sharp & dohme llc rahway nj usa does not accept unsolicited assistance from search firms for employment opportunities all cvs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company no fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place where agency agreements are in place introductions are position specific please no phone calls or emails employee status project temps fixed term relocation visa sponsorship travel requirements flexible work arrangements hybrid shift valid driving license hazardous material(s) required skills accountability accountability adaptability administrative policies adverse event reporting system clinical research methods clinical site management clinical study management clinical testing clinical trial planning clinical trials analysis clinical trials monitoring data analysis data reporting documentations early clinical development good clinical data management practice gcdmp good clinical practice gcp human resources policies management process medical research pharmacovigilance policy development protocol adherence recruiting preferred skills job posting end date 08/29/2025 - a job posting is effective until pm on the day before the ...
Operar en las areas logísticas de las bodegas a nivel nacional, asegurando eficiencia en los procesos de recepción, almacenamiento, alistamiento y despacho, así como el cumplimiento de los indicadores de servicio y productividad. responsabilidades principales: supervisar y garantizar el buen funcionamiento diario de las bodegas a nivel nacional. implementar estrategias para optimizar recursos, reducir costos y mejorar la productividad. liderar y motivar al equipo de fulfillment en cada ubicación. asegurar el cumplimiento de los procedimientos operativos y logísticos. ser el enlace principal con clientes que usan los servicios de fulfillment. garantizar el control de inventarios y cumplimiento de indicadores (kpi). requisitos: tecnólogo o profesional en logística, ingeniería o áreas afines. mínimo 1 año de experiencia liderando bodegas o centros de distribución. conocimiento en gestión de inventarios, erp/wms y procesos logísticos. disponibilidad para viajar. tipo de puesto: tiempo completo...
Job description under the direction of the global data operations (gdo) leadership, the gdo operations manager is responsible for leading senior clinical data managers (scdms) and clinical data managers (cdms) in operations tasks, both strategic and tactical in nature, within a data management center (dmc). they are responsible for ensuring the consistent execution of quality processes and deliverables and managing the workload and development of their direct staff. encourages effective interaction of dmc staff with business partners to achieve common objectives. primary activities include, but are not limited to: direct line management of scdm and cdms. talent management and performance management of teams with more than 10 members escalates to appropriate leadership/management as needed as risks and needs arise in the business increases functional effectiveness by supporting departmental efforts to simplify and standardize procedures to the greatest extent possible, sharing best practices and participating or leading in continuous improvement efforts. participates in or leads gdo business excellence networks (bens)gdo improvement efforts, gdo and/or gdms special initiatives as needed facilitates and/or participates in management and functional area meetings, contributing expertise when necessary, through formal or informal presentations. keeps abreast of process and technology changes both within and outside of the company that may impact staff. may support any other projects or perform any other data management task deemed appropriate by management. supports gdo manageme...
Senior manager data integration page is loaded senior manager data integration apply remote type hybrid locations col - cundinamarca - bogotá (colpatria) time type full time posted on posted 12 days ago time left to apply end date: july 31, 2025 (2 days left to apply) job requisition id r352979 job description join our dynamic team as a senior manager data integration! in this role, you will play a vital part in leading and directing our functional area. you will be responsible for overseeing business deliverables, interpreting performance metrics, and ensuring the success of your team while aligning objectives with the broader goals of the organization. we are seeking a motivated individual who is passionate about fostering team development and driving performance. if you possess strong leadership capabilities and are ready to take the next step in your career, we encourage you to apply and join our innovative environment focused on excellence. key responsibilities: lead and manage direct reports, setting priorities and developing performance objectives that align with organizational goals. assign work and ensure team members receive necessary training for effective performance. motivate staff by managing workloads realistically, anticipating challenges, and elevating complex issues when needed. conduct regular performance assessments, provide constructive feedback, and facilitate annual appraisals for your team. support career development by collaborating with staff on development plans and growth opportunities. participate in recruiting efforts and may supervise continge...
Join to apply for the ehs/fm coordinator role at merck group join to apply for the ehs/fm coordinator role at merck group work your magic with us! ready to explore, break barriers, and discover more? we know you’ve got big plans – so do we! our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in healthcare, life science, and electronics. together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. that's why we are always looking for curious minds that see themselves imagining the unimaginable with us. ehs/fm coordinator your role: as an environmental, health, safety & security (ehs) coordinator , you will be responsible for implementing, monitoring, and continuously improving programs related to occupational hygiene, workplace safety, environmental compliance, and physical security across our facilities in colombia. a key part of your role will involve coordinating external facility management services and occupational health providers, ensuring full compliance with local regulations and internal global standards, while guaranteeing a safe and efficient site operation. your responsibilities will include conducting internal audits and inspections, preparing and submitting regulatory reports, and leading employee training programs on safety, environmental practices, and emergency response. you will oversee waste management processes, monitor adherence to sustainability objectives, and ensure compliance with sg-sst (occupational health and safety...
Job description join our dynamic team as a senior manager data integration! in this role, you will play a vital part in leading and directing our functional area. you will be responsible for overseeing business deliverables, interpreting performance metrics, and ensuring the success of your team while aligning objectives with the broader goals of the organization. we are seeking a motivated individual who is passionate about fostering team development and driving performance. if you possess strong leadership capabilities and are ready to take the next step in your career, we encourage you to apply and join our innovative environment focused on excellence. key responsibilities: lead and manage direct reports, setting priorities and developing performance objectives that align with organizational goals. assign work and ensure team members receive necessary training for effective performance. motivate staff by managing workloads realistically, anticipating challenges, and elevating complex issues when needed. conduct regular performance assessments, provide constructive feedback, and facilitate annual appraisals for your team. support career development by collaborating with staff on development plans and growth opportunities. participate in recruiting efforts and may supervise contingent or temporary workers. enhance functional effectiveness by conducting meetings, sharing best practices, and leading continuous improvement initiatives. stay updated on process, technology, and regulatory changes, contributing to the development of standard operating procedures. requirements: b...
The sr. scientist drug safety will perform in line medical safety review of individual case safety reports (icsrs) reports and other ae reports of interest: 1. as required per sop and in conjunction with the icmr physician/management and/or therapeutic area team lead performs adverse experience reports review from specified sources in the safety database for regulatory reporting purposes 2. apply knowledge of safety profiles for the adverse experience reports review 3. develop working knowledge of pharmacovilance and regulatory reporting of icsrs 4. consult with the icmr physician/management and/or therapeutic area team lead for cases requiring additional clinical or safety subject matter expertise 5. may perform medical review of other reports of adverse events as required in conjunction with the icmr physician/management and/or therapeutic area team lead 6. may perform icsr follow up activities in conjunction with the icmr physician/management and/or therapeutic area team lead 7. may participate in process, quality, innovation, technology and other business-related activities under the guidance of icmr physician/management 8. may participate on special projects or rotational assignments within or outside of icmr the icmr associate with oversight from the icmr physician/management and/or therapeutic area team lead, may work closely and collaboratively with colleagues in other departments in the company, including but not limited to: global and us pharmacovigilance, global pharmacovigilance case management, and clinical safety & risk management. education: - adva...
Aplica tu magia con nosotros estás listo para explorar, romper barreras y descubrir mucho más? sabemos que tienes grandes planes. nosotros, también, innovar con la ciencia y la tecnología para enriquecer la vida de las personas con las soluciones en healthcare, life science y electronics apasiona a nuestros colegas en el mundo entero. juntos, soñamos en grande y compartimos el entusiasmo por cuidar a una gran diversidad de personas, clientes, pacientes y al planeta. por eso, siempre buscamos mentes curiosas que imaginen lo nunca visto con nosotros. unidos como uno solo para los pacientes: nuestra meta en healthcare es ayudar a crear, mejorar y prolongar vidas. creamos tratamientos, dispositivos inteligentes y tecnologías innovadoras en campos terapéuticos como la oncología, la neurología y la fertilidad. nuestros equipos colaboran en 6 continentes con pasión y una curiosidad incesante con el objetivo de ayudar a los pacientes en cada etapa de su vida. unirte a nuestro equipo de healthcare significa formar parte de una cultura de trabajo diversa, inclusiva y flexible, que ofrece fantásticas oportunidades para el desarrollo personal y profesional en todo el planeta. bienvenidos a merck. nos interesa tener en nuestro equipo de trabajo personas competitivas, empoderadas y propositivas. que se caractericen por ser agentes de cambio, orientados al futuro y resultados; con valores de responsabilidad, respeto, transparencia y, especialmente, ganas de aprender. requisitos adicionales: - manejo de herramientas de office (excel, word, power point). - manejo de p...
Las mejores invenciones no se llevarían al mercado sin la gestión de proyectos y el apoyo administrativo adecuados. nuestros equipos administrativos, entrelazados en cada parte de la organización, aseguran que nuestros conceptos se hagan realidad. realiza actividades de seguimiento de los indicadores de desempeño clave del área (calidad, cumplimiento, productividad, entrenamiento para el equipo general) en diferentes bases de datos y formatos de presentación de datos.realiza actividades de inventario. asiste en logística durante las actividades dentro y fuera de la oficina. nuestra división de salud humana mantiene una ideología que consiste en “primero el paciente, los beneficios más tarde”. la organización está compuesta por ventas, marketing, acceso al mercado, análisis digitales y profesionales comerciales a los que les apasiona su papel de llevar nuestros medicamentos a nuestros clientes de todo el mundo. **quiénes somos ** se nos conoce como merck & co., inc., rahway, nueva jersey, ee. uu., en estados unidos y canadá, y como msd en el resto del mundo. durante más de un siglo hemos estado inventando para la vida, desarrollando fármacos y vacunas para muchas de las enfermedades más difíciles del mundo. actualmente, nuestra empresa sigue estando a la vanguardia de la investigación para ofrecer soluciones de salud innovadoras y avanzar en la prevención y tratamiento de enfermedades que amenazan a personas y animales de todo el mundo. **lo que buscamos ** imagina levantarte por la mañana para hacer algo tan importante como lo es ayudar a salvar y mejorar vi...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, pharmaceutical chemist * 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), acknowledgm...
Operar en las areas logísticas de las bodegas a nivel nacional, asegurando eficiencia en los procesos de recepción, almacenamiento, alistamiento y despacho, así como el cumplimiento de los indicadores de servicio y productividad. responsabilidades principales: - supervisar y garantizar el buen funcionamiento diario de las bodegas a nivel nacional. - implementar estrategias para optimizar recursos, reducir costos y mejorar la productividad. - liderar y motivar al equipo de fulfillment en cada ubicación. - asegurar el cumplimiento de los procedimientos operativos y logísticos. - ser el enlace principal con clientes que usan los servicios de fulfillment. - garantizar el control de inventarios y cumplimiento de indicadores (kpi). requisitos: - tecnólogo o profesional en logística, ingeniería o áreas afines. - mínimo 1 año de experiencia liderando bodegas o centros de distribución. - conocimiento en gestión de inventarios, erp/wms y procesos logísticos. - disponibilidad para viajar. tipo de puesto: tiempo completo...
Aplica tu magia con nosotros estás listo para explorar, romper barreras y descubrir mucho más? sabemos que tienes grandes planes. nosotros, también, innovar con la ciencia y la tecnología para enriquecer la vida de las personas con las soluciones en healthcare, life science y electronics apasiona a nuestros colegas en el mundo entero. juntos, soñamos en grande y compartimos el entusiasmo por cuidar a una gran diversidad de personas, clientes, pacientes y al planeta. por eso, siempre buscamos mentes curiosas que imaginen lo nunca visto con nosotros. **qué haces**: - planear, organizar, dirigir y controlar las actividades y estrategias orientadas a la generación de mayor comercialización de los productos del negocio life science. - responsable del cumplimiento de las cuotas de ventas y promoción planificadas, según las zonas asignadas y tomando acciones de ser necesarias, con el fin de asegurar el cumplimiento de los objetivos trazados. - liderar un equipo de profesionales y es responsable por sus resultados. responsable de la gestión del día a día de los colaboradores a su cargo, el establecimiento de objetivos, desarrollo, evaluación de desempeño, compensaciones, etc. - apoyar al gerente general en realizar la planificación estratégica del negocio life science, de acuerdo a la metodología establecida, y apoyarlo en divulgar a los colaboradores y realizar seguimiento a la misma. - ejecutar las acciones tácticas que aseguren el cumplimiento de los objetivos de ventas. - planificar el trabajo, supervisar pipeline en sfdc, seguimiento y ejecución de proyectos ...
Msd latam bogota, d.c., capital district, colombia join or sign in to find your next job join to apply for the assoc. dir., clinical data mgmt role at msd latam get ai-powered advice on this job and more exclusive features. job description under the direction of the global data operations (gdo) leadership, the gdo operations manager is responsible for leading senior clinical data managers (scdms) and clinical data managers (cdms) in operations tasks, both strategic and tactical, within a data management center (dmc). they ensure the consistent execution of quality processes and deliverables, manage workload and staff development, and foster effective interactions with business partners to achieve objectives. primary activities include, but are not limited to - direct line management of scdms and cdms. - talent and performance management of teams with more than 10 members. - escalate risks and needs to leadership as they arise. - support departmental efforts to simplify and standardize procedures, share best practices, and participate in continuous improvement initiatives. - participate in or lead gdo business excellence networks (bens) and special initiatives. - contribute to management and functional meetings through presentations and expertise sharing. - stay updated on process and technology changes impacting staff. - support other projects or data management tasks as deemed appropriate. - assist gdo management in setting objectives and leading the team to achieve business goals. - lead or participate in cross-divisional projects and initiatives. - train staff on ...
Msd latam bogota, d.c., capital district, colombia join or sign in to find your next job join to apply for the assoc. dir., clinical data mgmt role at msd latam get ai-powered advice on this job and more exclusive features. job description under the direction of the global data operations (gdo) leadership, the gdo operations manager is responsible for leading senior clinical data managers (scdms) and clinical data managers (cdms) in operations tasks, both strategic and tactical, within a data management center (dmc). they ensure the consistent execution of quality processes and deliverables, manage workload and staff development, and foster effective interactions with business partners to achieve objectives. primary activities include, but are not limited to direct line management of scdms and cdms. talent and performance management of teams with more than 10 members. escalate risks and needs to leadership as they arise. support departmental efforts to simplify and standardize procedures, share best practices, and participate in continuous improvement initiatives. participate in or lead gdo business excellence networks (bens) and special initiatives. contribute to management and functional meetings through presentations and expertise sharing. stay updated on process and technology changes impacting staff. support other projects or data management tasks as deemed appropriate. assist gdo management in setting objectives and leading the team to achieve business goals. lead or participate in cross-divisional projects and initiatives. train staff on business processes, operation...
Job description the pharmacovigilance specialist is responsible for ensuring adherence to all applicable regulations, company policies and procedures. the specialist, pv may be designated by the pv lead to serve as the back-up (bu) local qualified person for pv (qppv) / bu local pv contact / bu local responsible pv person as required per local pv legislation. when designated, in the absence of the pv lead, they may manage day-to-day pv activities and serve as their back-up with supervision by a higher-level manager, as required. requirements: *education: chemicals, p harmaceutical chemist * 2+ years of experience in pharmacovigilance *knowledge in adverse events, pharmacovigilance regulations, follow-up with patients. *knowledge in excel, power bi. *english - advanced level activities: 1. responsible for execution of local pv processes and activities in collaboration with applicable internal functional areas and external parties, ensuring alignment with local legislation and local/regional/global company procedures and policies. activities may include but are not limited to management and negotiation of local pv agreements, local due diligence activities, post approval safety monitoring program (psmp) implementation, scheduling and coordinating aggregate safety report submissions, conducting local training, review of local initiatives for compliance with pv requirements, communication of safety issues. 2. responsible for day-to-day adverse events case management which may include case intake, translations (english and/or local language (as applicable)), acknowledgments, fol...
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