Clinical Trials Regulatory Manager

We are seeking a highly organized and detail-oriented Clinical Operations Specialist to join our team at Worldwide Clinical Trials.About the Role:The Clinical Operations Specialist will be responsible for ensuring all daily aspects of operational work related to rater selection, certification/qualification, training content, scale acquisition, surveillance...

Company Overview:Worldwide Clinical Trials (WCT) is a leading global contract research organization that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications.The company has a dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, which...

Job OverviewWe are seeking a highly skilled Regulatory Affairs Professional to join our team at Worldwide Clinical Trials. In this role, you will be responsible for planning, initiating, and tracking documents required for regulatory submissions, as well as coordinating with local investigators and key site personnel.About the RoleThis is a full-time...

About the RoleWe are seeking a highly skilled Regulatory Affairs Expert to join our team at Worldwide Clinical Trials.Job DescriptionIn this role, you will be responsible for planning, initiating and tracking documents required for regulatory submissions. You will also be involved in collecting essential documents, reviewing country/site/EC requirements, and...

Senior Regulatory Affairs SpecialistWe're seeking a highly skilled Clinical Trials Regulatory Affairs Expert to join our team at ICON Plc. This is an exciting opportunity to leverage your expertise in regulatory affairs and contribute to the success of our clinical trials.About the Role:Lead the preparation, submission, and maintenance of regulatory...

**About MEX Fortrea Clinical Development Mexico**: We are a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. Our team provides pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions...

At ICON plc, we're seeking a skilled Senior Regulatory Affairs Specialist with experience in clinical trials to join our team.This role will play a pivotal part in ensuring regulatory compliance and facilitating the successful execution of clinical trials, contributing to the advancement of innovative treatments and therapies.The estimated salary for this...

We are seeking a seasoned Clinical Trials Regulatory Affairs Specialist to join our team at ICON plc, a world-leading healthcare intelligence and clinical research organization. Located in Mexico City, this role offers a unique blend of work flexibility and professional growth opportunities.About the Role:The successful candidate will play a pivotal part in...

Job OverviewWe are seeking a highly skilled Global Clinical Trials Manager to join our team at Eli Lilly and Company.About the RoleThe successful candidate will lead and manage a team of clinical research professionals within the country, collaborating with business partners to ensure clinical trials/studies across all therapeutic areas are executed in...

At ICON, we are seeking a Senior Regulatory Affairs Specialist to join our team in Mexico City.The ideal candidate will have a strong background in clinical trials and regulatory affairs, with experience in preparing and submitting regulatory documents.We offer a competitive salary of $95,000 per year, plus benefits such as annual leave entitlements, health...

OverviewEli Lilly and Company, a global healthcare leader, is seeking a highly skilled Clinical Trials Leader and Team Manager to join our team. This role will be responsible for leading and managing a team of Clinical Research Leads within the country, collaborating with business partners to ensure clinical trials/studies are executed in accordance with...

Worldwide Clinical Trials (Worldwide) is a leading global contract research organization that works in partnership with biotechnology and pharmaceutical companies to create customized solutions for advancing new medications.We are seeking a highly skilled Clinical Assessment Specialist to join our team. As a key member of the Clinical Assessment Technologies...

Job SummaryWe are seeking a seasoned Regulatory Affairs Specialist to lead the preparation, submission, and maintenance of regulatory documents for clinical trials. The ideal candidate will have extensive experience in the pharmaceutical or biotech industry and possess strong knowledge of global regulatory requirements and guidelines.About the RoleDevelop...

We are seeking a highly skilled Clinical Data Manager to join our team at ICON Plc. As a key member of our clinical data management group, you will play a vital role in ensuring the success of our clinical trials.About ICON Plc:Company Overview:ICON plc is a world-leading healthcare intelligence and clinical research organization. Our mission is to shape the...

Job OverviewAs a Regulatory Compliance Specialist, you will play a crucial role in ensuring that clinical trials are conducted in accordance with regulatory requirements and guidelines. Under moderate supervision, you will execute the feasibility, site identification, regulatory, start-up, and maintenance activities at the regional or country level.Key...

Company OverviewWorldwide Clinical Trials is a global, midsize Contract Research Organization (CRO) that pushes boundaries and innovates to find cures for persistent diseases. We prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity.We're committed to hiring the best professionals from all...

At Eli Lilly and Company, we unite innovation with expertise to drive meaningful advancements in healthcare. We are a global pharmaceutical leader headquartered in Indianapolis, Indiana.We're looking for an exceptional individual to lead our clinical trials operations in-country, ensuring seamless execution of clinical trials across all therapeutic areas. As...

**Job Summary**As a Clinical Trial Manager with Syneos Health, you will be responsible for overseeing site management, clinical monitoring, and central monitoring deliverables with a focus on patient safety, protocol/GCP/regulatory compliance, and data integrity.**Key Responsibilities**Responsible for site management oversight, clinical monitoring, and...

Job SummaryMEX Labcorp Clinical Development, S. de R.L. de C.V. is seeking a highly skilled Clinical Research Manager to lead clinical trials and drive business growth. As a key member of our clinical operations team, you will be responsible for project management, protocol execution, and ensuring compliance with regulatory requirements.Key...

About the Role:As a Clinical Trials Specialist at Syneos Health Clinical, you will play a crucial role in ensuring the success of our clinical trials. Your primary responsibility will be to conduct site qualification, initiation, monitoring calls, and close-out visits for remote sites.Responsibilities:Conduct site qualification, initiation, monitoring calls,...