Regulatory Specialist for Clinical Research

About the RoleMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly skilled Clinical Research Manager to lead the execution of clinical trials in our region. As a key member of our team, you will be responsible for managing trial operations, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to...

About the RoleMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly skilled Clinical Research Manager to lead our clinical trials operations in Mexico. As a key member of our team, you will be responsible for managing clinical trials from feasibility to close-out, ensuring compliance with regulatory requirements and company standards.Key...

Job OverviewAs a leading global contract research organization (CRO), Fortrea is seeking a highly motivated and detail-oriented Clinical Trials Specialist to join our team. In this role, you will be responsible for coordinating and collecting data and information required by regulatory authorities, including the preparation of study documentation and...

**About the Role**Worldwide Clinical Trials is seeking a highly organized and detail-oriented Clinical Operations Specialist to join our team. As a Clinical Operations Specialist, you will be responsible for carrying out daily aspects of operational work related to rater selection, rater certification/qualification, rater training content, scale acquisition,...

Job Title: Clinical Research MonitorAt AbbVie, we are seeking a highly skilled Clinical Research Monitor to join our team. As a Clinical Research Monitor, you will play a critical role in ensuring the quality and integrity of our clinical trials.Key Responsibilities:Conduct on-site monitoring visits to ensure compliance with Good Clinical Practice (GCP) and...

About the RoleMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly motivated and experienced Clinical Research Manager to join our team. As a key member of our clinical operations team, you will be responsible for managing clinical trials from feasibility to close-out, ensuring timely and efficient execution of studies.Key...

**About the Role**We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Worldwide Clinical Trials. As a key member of our team, you will be responsible for planning, initiating, and tracking documents required for regulatory submissions, essential documents collection, review, and provision of country/site/EC requirements to...

Clinical Research Opportunities at PSI CRO **About the Role** As a Clinical Research Associate at PSI CRO, you will have the opportunity to work on a variety of clinical studies in different therapeutic indications. Our team is committed to delivering high-quality results and providing a supportive environment for our employees to grow and develop in their...

Covance Latinoamérica: Clinical Research AssistantWe are seeking a highly motivated and organized Clinical Research Assistant to join our team in Mexico. As a Clinical Research Assistant, you will play a key role in the success of our clinical trials by providing administrative support to our project team and study sites.Key Responsibilities:Act as the...

Regulatory & Start Up SpecialistWe are seeking a highly skilled Regulatory & Start Up Specialist to join our cFSP team in a Home Based role.Location: Argentina & MéxicoKey Responsibilities:Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating...

About Syneos Health ClinicalSyneos Health Clinical is a leading biopharmaceutical solutions organization that accelerates customer success. We bring together a unique combination of product development expertise and clinical research capabilities to deliver high-value insights and speed therapies to patients.Job SummaryWe are seeking a highly skilled...

Job OverviewMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly motivated Regulatory Compliance Specialist to join our team. As a key member of our clinical development team, you will be responsible for ensuring compliance with regulatory requirements and guidelines in the assigned countries.Key Responsibilities:Maintain awareness of...

Job OverviewMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly motivated and detail-oriented Regulatory Compliance Specialist to join our team. As a key member of our clinical development team, you will be responsible for ensuring compliance with regulatory requirements and guidelines in the assigned countries.Key...

Regulatory Affairs Specialist with Expertise in Clinical TrialsAt ICON Plc, we're seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory affairs team, you will be responsible for leading the preparation, submission, and maintenance of regulatory documents for clinical trials. Your expertise in clinical...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at Syneos Health Clinical. As a Clinical Research Associate, you will be responsible for performing site qualification, site initiation, interim monitoring, site management, and close-out visits to ensure regulatory, ICH-GCP, and protocol compliance.Key...

Job Title: Senior Regulatory Affairs Specialist with Experience in Clinical TrialsJob Summary:We are seeking a Senior Regulatory Affairs Specialist to join our team at 520 ICR Mexico - MEX. As a Senior Regulatory Affairs Specialist, you will play a key role in ensuring regulatory compliance and facilitating the successful execution of clinical trials.Key...

Job Title: Clinical Research AssociateAs a Clinical Research Associate at ICON Plc, you will be part of a dynamic team that is dedicated to delivering high-quality clinical research services to our clients. We are seeking a highly motivated and experienced individual to join our team as a Clinical Research Associate.Job Summary:The Clinical Research...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for performing and coordinating all aspects of the clinical monitoring and site management process.Key ResponsibilitiesConduct remote or on-site visits to assess protocol and regulatory compliance and manage...

Job OverviewAt IQVIA, we are seeking a skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for conducting site monitoring visits to ensure that sites are conducting studies and reporting data as required by the study protocol, applicable regulations, and sponsor requirements.Key...

{"Job OverviewAs a Senior Clinical Research Associate at IQVIA, you will be responsible for ensuring the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Your expertise will be utilized to drive site recruitment plans, administer protocol and related study training, and...