Join our vibrant and diverse global team at global data operations, where we are dedicated to shaping the future of clinical data management. as a recent graduate in b.a. or b.s. degree biomedical engineer, bioengineer, microbiology and bioanalysis, biology and bacteriology. discipline, this is your opportunity to make an impact in a dynamic and growing industry. our ideal candidate: at least b.a. or b.s. degree biomedical engineer, bioengineer, microbiology and bioanalysis, biology and bacteriology , with 2 years of formal work experience . knowledge and skills: -excellent planning and time management skills -able to work under pressure in a changing flexible environment -critical thinking and analytic skills -good communication skills -fluent oral and written english skills. -preferred: background of data science skills in the context of healthcare current employees apply current contingent workers apply 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. e...
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 management team to set ...
Current employees apply current contingent workers apply 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 {+ 5 more} preferred skills: job posting end date: 08/29/2025 *a job posting is effective until 1...
This role is accountable for performance and compliance for assigned protocols in a country in compliance with ich/gcp and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. under the oversight of the sr. com, head coms or crd, the person is responsible for budget/finance aspects, for execution and oversight of clinical trial country submissions and approvals and to ensure site ready. responsibilities include, but are not limited to: • ownership of country and site budgets. development, negotiation and completion of clinical trial research agreements (ctra). • oversees and tracks clinical research-related payments. payment reconciliation at study closeout. oversees fcpa, dps/ofac, and maintenance of financial systems. financial forecasting in conjunction with sr.com /other roles. • executes and oversees clinical trial country submissions and approvals for assigned protocols. • develops local language materials including local language informed consents and translations. interacts with irb/iec and regulatory authority for assigned protocols. • manages country deliverables, timelines and results for assigned protocols to meet country commitments. responsible for quality and compliance in assigned protocols in country. • contributes to the development of local sops. oversees ctcs as applicable. • coordinates and liaises with crm, ctc, cra, (finance and legal if appropriate) to ensure country deliverables are obtained for submissions, budgets, ctras and local milestones. collaborates closel...
Defender el posicionamiento de medicamentos entre los profesionales de la salud desarrollando e implementando estrategias para consolidar el posicionamiento de la compañía, generar interés y construir una reputación positiva a través de diversos canales . funciones: desarrollo e implementación de estrategias que contribuyan a la defensa de posicionamiento de medicamentos. análisis y seguimiento de kpi de las estrategias implementadas colaboración con las diferentes áreas de la compañía a fin de tener una visión 360 del negocio e impactar todos los stakeholders necesarios. conocimiento y análisis de los competidores, a fin de poder gestionar estrategias de defensa de posicionamiento en el país. cumplimiento de políticas: asegurar que todas las actividades de awareness cumplan con las normativas y leyes aplicables en la industria farmacéutica fomentar relaciones con líderes de opinión y asociaciones médicas para aumentar la credibilidad y visibilidad de la marca contribuir a los objetivos estratégicos de la compañía. alinear las iniciativas de optimización del funnel con los objetivos comerciales y de crecimiento de la compañía, definir kpis claros y medibles que contribuyan directamente a los objetivos de ingresos, adquisición, retención y satisfacción del stakeholders. liderar y gestionar proyectos planificar, organizar y dar seguimiento a proyectos de optimización, asegurando cumplimiento de plazos y calidad. requisitos: profesional en marketing, administración, comunicación social, entre otros. experiencia profesional de mínimo 1 año en cargos administrativos, preferiblem...
Maximizar la conversión de profesionales de la salud y tomadores de decisión mediante la optimización estratégica del la información y evaluación del producto, facilitando la adopción y prescripción responsable de los medicamentos de oncología. funciones: mapear y analizar el recorrido de los stakeholders: i dentificar y comprender las etapas clave que atraviesan los profesionales de la salud y otros tomadores de decisión (hospitales, aseguradoras) desde el primer contacto hasta la prescripción o compra. detectar puntos de fricción y abandono: usar datos y feedback para encontrar barreras en el proceso de evaluación y adopción del producto, como dudas sobre eficacia, costos, o procesos regulatorios. optimizar materiales y canales de comunicación: asegurar que la información científica, comercial y regulatoria llegue de forma clara, precisa y atractiva a médicos, farmacéuticos, administradores hospitalarios y otros stakeholders. colaborar con equipos multidisciplinarios: trabajar con marketing, medical, ventas, regulatorio y legal para garantizar que las estrategias sean efectivas y cumplan con normativas. monitorear y reportar métricas clave: medir el desempeño del funnel (tasa de conversión, tiempo de decisión, engagement) y generar reportes para la toma de decisiones estratégicas. garantizar el cumplimiento regulatorio: supervisar que todas las acciones y contenidos respeten las normativas locales e internacionales aplicables a la promoción farmacéutica liderar y gestionar proyectos: planificar, organizar y dar seguimiento a proyectos de optimización, asegurando cumplimie...
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