Field Clinical Engineer

As a leading global contract research organization, Fortrea is seeking a highly skilled Clinical Trials Operations Specialist to support our pharmaceutical, biotechnology, and medical device customers.Typical AccountabilitiesSchedule and manage clinical trials, ensuring compliance with regulatory requirements.Develop and implement efficient clinical trial...

Key ResponsibilitiesWe are seeking a highly skilled Clinical Trial Feasibility Specialist to join our team at Novo Nordisk. As a key member of our China CDC team, you will be responsible for developing and executing the early planning and clinical trial feasibility strategy.Develop and execute the early planning and clinical trial feasibility strategy in...

Key ResponsibilitiesWe are seeking a highly skilled Feasibility Manager to join our team at Novo Nordisk. As a key member of our China CDC team, you will be responsible for developing and executing the early planning and clinical trial feasibility strategy.Develop and execute the early planning and clinical trial feasibility strategy in China CDC.Deliver...

Job Title: Field MPSAt Stryker (Beijing) Healthcare Products Co. Ltd, we are seeking a highly skilled and experienced Field MPS Representative to join our team. As a Field MPS Representative, you will play a critical role in providing clinical sales support to our end-users and delivering on-site guidance and assistance during surgical procedures.Key...

Major Responsibilities General: Familiarity with products, clinical data and clinical information regarding our leadless technology. (e.g. products, related surgeries, follow-up, patient indications, reimbursement, related literature, etc.) Provide appropriate clinical support based on the physician's experience with leadless technology. Provide...

Job Description:Clinical Research Associate Trainee (CRA Trainee) project is a professional talent cultivation program established by IQVIA China, based on the global training system, combining domestic business development and needs. The program aims to train and send qualified clinical monitors to business teams through efficient and professional training....

Key ResponsibilitiesWe are seeking a highly skilled Feasibility Manager to join our team at Novo Nordisk A/S.Develop and execute the early planning and clinical trial feasibility strategy in China CDC.Deliver timely and high-quality early planning and feasibility activities for portfolio and clinical trials in CKAD and RareD TA.Act as the primary point of...

Job Title: FSP-SCRA I Job Summary:Fortrea is seeking a Clinical Research Associate I to support the execution of clinical trials across multiple therapeutic areas. The successful candidate will be responsible for conducting site visits, managing study documentation, and ensuring compliance with regulatory requirements.Essential Responsibilities:Conduct site...

Are you passionate about driving innovation in the life sciences industry? Do you want to contribute to the development of new treatments for patients with chronic diseases? We're seeking a talented Clinical Research Associate to join our team at Novo Nordisk.About the RoleAs a Clinical Research Associate, you will be the primary point of contact between...

Unlocking Excellence in Clinical TrialsAt Parexel, we're committed to delivering exceptional results in clinical trials. As a Risk Management Specialist - Clinical Trials, you'll play a vital role in ensuring the success of our studies.Key Responsibilities:Develop and implement risk assessment strategies for clinical trialsCollaborate with cross-functional...

Key ResponsibilitiesDevelop and execute the early planning and clinical trial feasibility strategy in China CDC, ensuring timely and high-quality delivery of portfolio and clinical trials in CKAD and RareD TA.Act as the primary point of contact for internal and external stakeholders on clinical trial early stage discussions and decisions in China...

Key ResponsibilitiesAs a key member of our team, you will be responsible for developing and executing the early planning and clinical trial feasibility strategy in China CDC. This will involve delivering in-time and in-quality early planning and feasibility activities for portfolio and clinical trials in CKAD and RareD TA.You will serve as the main point of...

Key ResponsibilitiesDevelop and execute the early planning and clinical trial feasibility strategy in China CDC, ensuring timely and high-quality delivery of portfolio and clinical trials in CKAD and RareD TA.Act as the primary point of contact for internal and external stakeholders on clinical trial early stage discussions and decisions in China...

Key ResponsibilitiesWe are seeking a highly skilled and experienced Clinical Trial Feasibility Specialist to join our team at Novo Nordisk. As a key member of our China CDC team, you will be responsible for developing and executing the early planning and clinical trial feasibility strategy in China.Key Responsibilities:Develop and execute the early planning...

Key ResponsibilitiesWe are seeking a highly skilled Feasibility Manager to join our team at Novo Nordisk. As a key member of our China CDC team, you will be responsible for developing and executing the early planning and clinical trial feasibility strategy.Develop and execute the early planning and clinical trial feasibility strategy in China CDC.Deliver...

Key ResponsibilitiesWe are seeking a skilled Clinical Trial Feasibility Specialist to join our team at Novo Nordisk. The successful candidate will be responsible for developing and executing the early planning and clinical trial feasibility strategy in China CDC.Deliver in-time and in-quality early planning and feasibility activities for portfolio and...

Job SummaryFortrea is seeking a highly motivated and detail-oriented Clinical Research Associate II to join our team in Chengdu. As a key member of our clinical operations team, you will be responsible for ensuring the integrity of clinical trials and providing high-quality support to our clients.Key ResponsibilitiesConduct routine monitoring and close-out...

Job Summary:IQVIA is seeking a Clinical Research Associate Trainee to join our team. As a CRA Trainee, you will be responsible for assisting in the conduct of clinical trials, ensuring compliance with regulatory requirements, and providing high-quality data to support the development of new medicines.Key Responsibilities:Assist in the planning, execution,...

PurposeThe primary goal of this position is to ensure the successful execution of clinical studies at AbbVie. This involves proactively identifying and resolving study-related issues at clinical sites, ensuring compliance with regulatory requirements, and maintaining high-quality data submission.ResponsibilitiesMonitor clinical site activities to ensure...

Job Title: Centralized Monitoring AssistantIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry.We are seeking a highly skilled and detail-oriented Centralized Monitoring Assistant to join our team. As a Centralized Monitoring Assistant, you will play a critical role in...