Link-Worldwide in Valle de Chalco Solidaridad is looking for a member of the Study Start Up Team. You will coordinate vital activities to prepare physicians for clinical trials involving investigational products. The ideal candidate will have a Bachelors
Link-Worldwide is hiring for a position focused on the planning and execution of clinical studies across Mexico. The role involves managing regulatory documents, collaborating on publications, and ensuring compliance with Good Clinical Practices.Applicants should have a medical, pharmacy, or
Fortrea is a leading integral contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience.We provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology
Link-Worldwide is looking for an entry level candidate to support clinical research by encouraging patient participation in studies for 6 months.This role involves conducting phone screens, maintaining a patient database, and meeting recruitment targets.The ideal candidate should possess
Link-Worldwide is seeking a candidate for a role focused on managing contracts and budgets for clinical site investigations in Valle de Chalco Solidaridad, Estado de México. The successful candidate will be responsible for negotiating contracts, preparing documentation,
Requisition Number: Employment Type: Regular Requisition NumberEmployment Type: Regular Who We Are We are a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the worlds most persistent diseases
ResponsibilitiesDesign and implement clinical trial protocols, conduct data analysis, and collaborate with cross‐functional teams to ensure effective study execution.QualificationsThe ideal candidate holds a Bachelors degree in a relevant scientific discipline and has experience in clinical research.BenefitsThe position offers a
Link-Worldwide is seeking a Study Start Up Associate I to support the initiation of clinical trials in Mexico City. The role involves coordinating with stakeholders for study approvals, maintaining regulatory compliance, and ensuring quality throughout the study start-up process. Ideal
At ICON, its our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients lives. Our
Company DescriptionJob DescriptionPurpose Statement:Collaborate with the coordination of planning, implementation, and conduction of local and general clinical studies (Post-Marketing Observational, Multi-Country Non-Interventional, Investigator Initiated, Non-AbbVie Sponsored Collaborative and Pharmacoeconomic) and Pre-Approval Access programs (PAAs) according to Abbvie business
Link-Worldwide in Valle de Chalco Solidaridad seeks a candidate for Trial Documentation & eTMF Management role focused on overseeing clinical trial documentation and ensuring compliance with electronic Trial Master File (eTMF) standards.The ideal candidate will have less
Link-Worldwide is seeking a SMA II to support clinical trial management in Mexico City. The successful candidate will ensure compliance with study protocols and work closely with internal teams and external stakeholders.This position requires a Bachelors degree and
SummarySupervisa la ejecución e interpretación de investigaciones de ensayos clínicos, actividades de recopilación de datos y operaciones clínicas. Establece y aprueba métodos científicos para el diseño e implementación de protocolos clínicos, sistemas de recopilación de datos
ICON plc is seeking a Project Manager, Laboratory to manage client relationships and oversee studies in a fast-paced environment. The role demands effective communication and responsibility for enhancing client satisfaction while adhering to Good Clinical Practice.Key responsibilities include
Link-Worldwide is hiring a SMA II based in Mexico City.You will play a critical role in supporting clinical trial management, ensuring compliance with study protocols, and liaising with internal teams and external stakeholders.This position requires a Bachelors degree
Link-Worldwide is looking for a Clinical Trial Administrator (CTA) to support the execution of clinical research projects. The role includes documenting and tracking study activities, maintaining documentation, and assisting with administrative tasks to ensure high-quality clinical data.The ideal candidate will
Link-Worldwide in Valle de Chalco Solidaridad is seeking a candidate to design and implement clinical trial protocols, conduct data analysis, and collaborate with cross-functional teams to ensure effective study execution.The ideal candidate should have a Bachelors degree in
Worldwide Clinical Trials is looking for a Team Lead for TMF Operations in Mexico, Ciudad de México.This pivotal role involves maintaining compliance with Trial Master Files and driving the objectives of Project Teams across various studies.As Team Lead,
Work Schedule:Standard (Mon-Fri)Environmental Conditions:OfficeJob Title:Project Support CoordinatorEmbark on an outstanding and rewarding career with Thermo Fisher Scientific Inc. as a Project Support Coordinator in our Information Technology department.This is an outstanding opportunity to play a pivotal
Job SummaryPerforms assigned activities within the country that lead to start-up of investigative sites in all phases of clinical trials.Responsible for delivery with oversight from Line Manager in areas such as investigator site contracts, ethics and regulatory