Clinical Trials Logistics Specialist

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job DescriptionAs a Clinical Trials Analyst II at Thermo Fisher Scientific, you will have the opportunity to lead and support our clients in the execution of clinical trials logistics. Your role will be crucial in ensuring the success of our clients' projects. Responsibilities:Support both...

Lead Clinical Trials Logistics at Thermo Fisher ScientificAs a Clinical Trials Analyst II at Thermo Fisher Scientific, you will play a key role in ensuring the success of our clients' projects by leading and supporting the flawless execution of logistics for clinical trials.Responsibilities:Support clients by understanding their specific requirements and...

Lead Clinical Trials Logistics at Thermo Fisher ScientificAs a Clinical Trials Analyst II at Thermo Fisher Scientific, you will play a key role in ensuring the success of our clients' projects by leading and supporting the flawless execution of logistics for clinical trials.Key Responsibilities:Support clients by understanding their specific requirements and...

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...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description As a Clinical Trials Analyst II at Thermo Fisher Scientific, you will have the opportunity to lead and support our clients in the execution of clinical trials logistics. Key responsibilities include supporting both foreign and domestic clients in the planning and execution of...

Job SummaryAs a Clinical Trials Analyst II at Thermo Fisher Scientific Inc., you will have the opportunity to lead and support our clients in the execution of logistics for clinical trials. Your role will involve working closely with clients to understand their specific requirements and providing logistical solutions to meet their...

Key Responsibilities:Support clients by understanding their specific requirements and providing logistical solutions.Develop and implement effective logistical strategies to meet client needs.Collaborate with cross-functional teams to ensure seamless execution of clinical trials.About the Role:This role is part of the Thermo Fisher Scientific team,...

Job SummaryWe are seeking a skilled Clinical Trial Operations Specialist to join our team at Iqvia.About the RoleThe successful candidate will be responsible for the local management of clinical trials, ensuring compliance with Sponsor SOPs, WIs, policies, codes of Good Clinical Practice (GCP), and local regulatory requirements.Key ResponsibilitiesPrepare...

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...

We are seeking a Clinical Trial Start-Up Specialist to advance clinical trial start-up activities by understanding client objectives and assisting in the development of the plan for country and site distribution.The ideal candidate will have a strong understanding of regulatory and submission processes in various countries and excellent written and verbal...

Job OverviewWe are seeking an experienced Site Network Development Specialist to join our Business Development team. This role is responsible for building and expanding the network of clients in the clinical trials industry.

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAs a Clinical Trials Analyst II at Thermo Fisher Scientific, you will have the opportunity to lead and support our clients in the execution of clinical trials logistics. You will play a key role in ensuring the success of our clients' projects by providing expert support and...

Job SummaryAs a Clinical Trials Analyst II at Thermo Fisher Scientific, you will play a key role in ensuring the success of our clients' projects by providing logistical solutions and support. Responsibilities:Support clients by understanding their specific requirements and providing tailored logistical solutions.Apply your knowledge of logistics services to...

We are seeking a highly skilled Clinical Trial Start-Up Specialist to join our team at ICON. As a key member of our team, you will be responsible for advancing clinical trial start-up activities by understanding client objectives and assisting in the development of plans for country and site distribution.The ideal candidate will have a strong background in...

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 Overview**The Clinical Trial Educator, based in our global network, will collaborate with trial coordinators and healthcare providers to provide information and education on clinical trial inclusion and exclusion criteria.This role requires working in partnership with CRAs and other field-based medical teams to develop tailored recruitment plans and...

{"**Job Title:** **Local Trial Manager** **Job Summary:** We are seeking a highly skilled and experienced Local Trial Manager to lead and manage the conduct of clinical trials from study start-up to close out at a country level in accordance with ICH-GCP and other applicable local regulations. **Key Responsibilities:** * Partner with global and local...

Supporting Clients GloballyWe are seeking a skilled Clinical Trials Analyst II to join our team at Thermo Fisher Scientific. In this role, you will be responsible for providing logistical support to both foreign and local clients, understanding their specific requirements, and delivering tailored solutions.Key Responsibilities:Collaborate with clients to...

Medpace, Inc. is seeking a full-time Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo. This position plays a key role in the clinical trial management process.Key Responsibilities:Efficiently manage and successfully execute clinical trial submissions.Collaborate with cross-functional teams to ensure timely and accurate...

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...