Senior Clinical Research Manager

Job SummaryClinical Trial Services, Inc. is seeking a highly skilled Clinical Research Associate Lead to join our team. As a Clinical Research Associate Lead, you will be responsible for overseeing the conduct of clinical trials at assigned sites, ensuring compliance with regulatory requirements, and providing guidance to site staff.Key...

About the Role:We are seeking a highly skilled Clinical Trial Manager II to join our team at ICON plc, a world-leading healthcare intelligence and clinical research organization. As a Clinical Trial Manager II, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of...

Principal Clinical Research AssociateJob SummaryCTI Clinical Trial Services, Inc. is seeking a highly skilled and experienced Principal Clinical Research Associate to join our team. As a key member of our clinical operations team, you will be responsible for overseeing the management of clinical trials, ensuring compliance with regulatory requirements, and...

Job Title: Clinical Trial Manager IIAt ICON Plc, we're committed to fostering an inclusive environment that drives innovation and excellence. We're seeking a highly skilled Clinical Trial Manager II to join our team and contribute to the advancement of inNvative treatments and therapies.Key Responsibilities:Collaborate with cross-functional teams to design...

Job Title: Regulatory Affairs At Intrials Clinical Research, we are seeking a highly skilled and experienced Regulatory Affairs professional to join our team.Primary Responsibilities:Manage the Regulatory & Study Start-up team in all aspects, with support from the Regulatory and Study Start-up Manager (RSM).Support RSM in defining metrics and KPIs for the...

Job Title: Regulatory Affairs SpecialistAbout the Role:We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Intrials Clinical Research. As a Regulatory Affairs Specialist, you will be responsible for managing regulatory and start-up activities for clinical trials in Latin America.Key Responsibilities:- Manage regulatory and...

Job Title: Lead Clinical Research AssociateJob Summary:In this role, you will oversee local clinical research activities, ensuring the protection of trial subjects' rights, safety, and well-being, as well as data quality and study compliance on a country/regional level.Key Responsibilities:Facilitate regional projects as Lead Clinical Research Associate and...

At Milestone One, we're on a mission to support clinical study sites in delivering stronger studies. To achieve this goal, we're seeking an experienced Senior Clinical Research Associate to join our team.About the RoleWe're looking for a highly skilled SCRA professional to find and build relationships with new clinical trial sites, actively promoting our...

Clinical Research Associate Job DescriptionAt Thermo Fisher Scientific, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for ensuring the integrity and quality of clinical trials. Your primary focus will be on monitoring and managing clinical trials, ensuring compliance...

This role is accountable for performance and compliance for assigned protocols in a country in accordance with regulations, policies, quality standards, and adverse event reporting requirements.The person is responsible for budget/finance aspects, execution, and oversight of clinical trial country submissions and approvals, and ensuring Site...

Key Responsibilities:As a Regulatory Submissions Manager at Medpace, you will play a vital role in the clinical trial management process. Your primary focus will be on efficiently managing and successfully completing regulatory submissions for our LATAM clinical trials.Key Skills and Qualifications:• Strong expertise in clinical trial management and...

**Job Overview**As a Clinical Research Associate, you will be responsible for ensuring the proper conduct of clinical trials at assigned sites. This includes performing site monitoring visits, administering protocol training, and evaluating the quality of study site practices.**Key Responsibilities:**Perform site monitoring visits to ensure compliance with...

Job Title: Clinical Research CoordinatorWe are seeking a highly motivated and organized Clinical Research Coordinator to join our team at IQVIA in Curitiba, Brazil. As a Clinical Research Coordinator, you will be responsible for supporting the site team with various administrative tasks, including verifying research study information, researching queries,...

Job OverviewWe are seeking a highly skilled Senior Clinical Research Project Lead to join our team at ODC Life Sciences. In this role, you will be responsible for managing the full project cycle, from start to completion, ensuring successful delivery within budget and with expected results.Key ResponsibilitiesDevelop and implement detailed clinical research...

Job DescriptionWe are seeking an experienced Global Clinical Trials Manager to join our team at Allucent. As a key member of our clinical operations department, you will be responsible for providing leadership and management to the Clinical Research Associates (CRAs) and other clinical functional groups in their day-to-day clinical trial activities.Your...

SAO Fortrea Brazil Limitada Clinical Trials AssistantWe are seeking a highly motivated and organized Clinical Trials Assistant to join our team in Fortrea, Brazil.About the JobThe Clinical Trials Assistant will be an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. This role will involve performing...

Job SummaryWe are seeking a highly skilled Clinical Research Associate to join our team at ICON Plc. As a Clinical Research Associate, you will be responsible for managing clinical trials and ensuring compliance with regulatory requirements.Key ResponsibilitiesManage clinical trials from initiation to close-outEnsure compliance with ICH GCP guidelines and...

Company OverviewPSI CRO is a leading Contract Research Organization with a strong presence in the industry, offering a perfect balance between stability and innovation to both clients and employees.Job ResponsibilitiesAs a Medical Monitor at PSI CRO, you will provide medical input to global clinical studies and advise the teams and business partners,...

Project Management AnalystAs a Project Management Analyst at IQVIA, you will play a crucial role in the delivery of clinical trials, working closely with clinical teams to improve patients' lives by bringing new drugs to the market faster. You will provide support to Project Leaders and Clinical Project Managers, helping to mitigate risk, control costs,...

Job Summary:We are seeking a highly skilled and experienced Clinical Trial Management Associate to join our team in a Senior Regional Clinical Trial Management Associate role.About the Role:As a Senior Regional Clinical Trial Management Associate, you will be responsible for supporting the Regional Clinical Study Manager in regional study delivery and...