Site Contracts Specialist With Experience In Clinical Trials Hybrid Mexico/Home Based Argentina

About Syneos HealthAt Syneos Health, we are a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of...

Job SummaryWe are seeking a highly skilled and experienced Site Manager to join our team at Johnson & Johnson. As a Site Manager, you will be responsible for ensuring the smooth execution of clinical trials at our investigative sites.Key ResponsibilitiesSite Management: Serve as the primary contact point between the Sponsor and the Investigational Site,...

Job SummaryNovasyte is seeking a highly skilled Site Solutions Specialist to join our team. As a Site Solutions Specialist, you will be responsible for providing exceptional support to our clients and ensuring the smooth execution of clinical trials.Key ResponsibilitiesProvide initial site communication and ensure timely and accurate payment...

About the RoleWe are seeking a highly skilled Clinical Specialist to join our team at Boston Scientific Corporation. As a Clinical Specialist, you will play a critical role in supporting the clinical trials process, ensuring compliance with regulatory and company guidelines, and providing training and education to physicians and hospital staff.Key...

About the RoleWe are seeking a highly skilled and detail-oriented Associate I, TMF Operations Specialist to join our team at Worldwide Clinical Trials. As a key member of our operations team, you will play a critical role in ensuring the quality and integrity of our clinical trial documents.Key ResponsibilitiesProcess Trial Master File (TMF) documents for...

Job Summary:We are seeking a highly skilled Clinical Trials Due Diligence Specialist to join our team at Syneos Health Clinical. As a key member of our team, you will be responsible for applying your technical expertise to complete and record assigned due diligence tasks.Key Responsibilities:Conduct thorough due diligence reviews of clinical trials and...

Job SummaryWe are seeking a highly skilled Clinical Trial Activation Specialist to join our team at ICON. As a Clinical Trial Activation Specialist, you will play a critical role in the successful execution of clinical trials by ensuring timely and efficient site activation.Key ResponsibilitiesOversee the day-to-day execution and site progress for all...

Job SummaryWe are seeking a highly organized and detail-oriented Regulatory Affairs Coordinator to join our team at Worldwide Clinical Trials, LLC. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring the smooth operation of our regulatory processes.Key ResponsibilitiesCoordinate and manage the compilation of...

Job SummaryWe are seeking a highly organized and detail-oriented Regulatory Affairs Coordinator to join our team at Worldwide Clinical Trials, LLC. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring the smooth operation of our regulatory processes.Key ResponsibilitiesCoordinate and manage the compilation of...

Job SummaryWe are seeking a highly skilled and experienced Clinical Project Manager to join our team at Novasyte. As a Clinical Project Manager, you will be responsible for the successful planning, implementation, and execution of clinical trials in the dermatology space.Key ResponsibilitiesManage projects of full scope, including regional and global...

Job SummaryWe are seeking a highly skilled Clinical Trial Site Relationship Manager to join our team at Novartis. As a key member of our Global Drug Development team, you will be responsible for ensuring the successful start-up of clinical trials at sites in Mexico.Key ResponsibilitiesManage site relationships and ensure timely start-up activities from...

Job SummaryWe are seeking a highly skilled Clinical Trial Manager to join our team at Icon. As a Clinical Trial Manager, you will be responsible for overseeing the planning, execution, and monitoring of clinical trials.Key ResponsibilitiesDevelop and implement clinical trial protocols and proceduresCollaborate with cross-functional teams to ensure trial...

Job OverviewAs a Software Development Engineer at Iqvia Argentina, you will be responsible for designing and developing software solutions that require general domain knowledge and specialized business experience. You will analyze user requirements and needs, and make decisions within general parameters under regular supervision.Key Responsibilities•...

About the RoleThe Structural Heart Field Clinical Specialist will provide day-to-day account management and clinical case support and education for assigned products and accounts in Mexico City. This role will drive sales growth for the product portfolio, provide guidance and training on TAVI and LAAO procedures, and be responsible for delivering target...

About ICON PlcICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, and government and public health organizations.Our MissionWe put our patients at the center of everything we do,...

About the RoleAt ICON Plc, we're committed to advancing and improving patients' lives through our work in clinical research. As a Project Assistant, you'll play a vital role in the running of multiple clinical trials, working closely with our team in Mexico City.Key Responsibilities:Assist with the development of project-specific procedure manuals and...

About the RoleAt ICON, we're committed to advancing and improving patients' lives through clinical research. As a Study Start Up Associate II, you'll play a critical role in ensuring that our research sites are prepared to start clinical trials of investigational products.Key ResponsibilitiesReview and negotiate clinical site investigator contracts and...

About the RoleWe are seeking a highly organized and detail-oriented Associate II, TMF Operations to join our team at Worldwide Clinical Trials. As a key member of our operations team, you will be responsible for the processing, maintaining, and archiving of essential documents in compliance with relevant Standard Operating Procedures, ALCOA principles,...

Job DescriptionJob Title: Clinical Research ManagerJob Summary:Fortrea is seeking a highly skilled Clinical Research Manager to join our team. As a Clinical Research Manager, you will be responsible for managing clinical trials from start to finish, ensuring that they are conducted in accordance with regulatory requirements and company standards.Key...

About the Role**Clinical Specialist/ Puebla/ Estimulación**We are seeking a highly skilled Clinical Specialist to join our team at Medtronic. As a Clinical Specialist, you will play a critical role in providing education and consulting services to our customers, while also supporting our sales team in developing and executing sales plans.Key...