Field Clinical Specialist

MAIN RESPONSIBILITIES 1. Clinical support: 40% of time 1) Develop a thorough understanding of advanced heart failure and HM3 as a treatment option. 2) Become fully trained and certified to support HeartMate 3 cases, including assessment of patient suitability and case planning 3) Optimize process regarding patient screening and procedure scheduling 4)...

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 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...

Job Summary:We are seeking a highly skilled Clinical Sales Specialist to join our team at Stryker (Beijing) Healthcare Products Co. Ltd. As a Clinical Sales Specialist, you will be responsible for providing clinical sales support to end-users, providing on-site guidance and assistance during surgical procedures, and driving continuous account growth.Key...

Job SummaryWe are seeking a highly skilled Clinical Sales Specialist to join our team at Stryker (Beijing) Healthcare Products Co. Ltd. As a Clinical Sales Specialist, you will be responsible for providing clinical sales support to end-users, providing on-site guidance and assistance during surgical procedures, and driving continuous account growth.Key...

Job SummaryWe are seeking a highly skilled Clinical Research Site Activation Specialist to join our team at IQVIA. As a key member of our clinical research operations team, you will be responsible for ensuring the successful activation of investigative sites for clinical trials.Key ResponsibilitiesServe as Single Point of Contact (SPOC) for investigative...

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...

Major ResponsibilitiesGeneral: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 educational...

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...

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...

Support the Preparation and Coordination of Clinical TrialsAt Thermo Fisher Scientific, we're committed to enabling our customers to make the world healthier, cleaner, and safer. As a Clinical Trials Specialist, you'll play a critical role in supporting the preparation and coordination of clinical trials, ensuring that our customers receive the highest...

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 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, ensuring timely and high-quality delivery.Deliver in-time and in-quality early planning and feasibility activities for portfolio and clinical trials in CKAD...

About the Role:The HGRAC Specialist is a key member of our team at Parexel, responsible for ensuring seamless HGRAC application processes for insourced and outsourced studies in China.Main Responsibilities:Submit and review HGRAC applications, including online application forms, paper documents, and dossier submissions, in accordance with HGRAC...

Unlock Your Potential as a Trial Activation Approval Specialist IIAt Thermo Fisher Scientific, we're committed to empowering our customers to make the world a healthier, cleaner, and safer place. As a Trial Activation Approval Specialist II, you'll play a vital role in bringing our mission to life by ensuring the smooth execution of clinical trials.Key...

MAIN PURPOSE OF ROLE Individual contributor that works under limited supervision. Applies subject matter knowledge. Requires capacity to understand specific needs or requirements to apply skills/knowledge. MAIN RESPONSIBILITIES • Responsible for promoting and/or selling the organization's products across multiple or non-specified channels in a...

Job SummaryParexel is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for implementing and monitoring clinical trials to ensure sponsor and investigator obligations are being met and are compliant with applicable local regulatory requirements and ICH GCP guidelines.Key...

Job Summary:IQVIA is seeking a Clinical Research Associate Trainee to join our team. As a Clinical Research Associate Trainee, you will be responsible for assisting in the conduct of clinical trials, ensuring compliance with regulatory requirements, and providing support to research teams.Key Responsibilities:Assist in the preparation and execution of...

Job Overview:IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are seeking a highly motivated and detail-oriented Clinical Research Associate Trainee to join our team.Key Responsibilities:Assist in the coordination and execution of clinical trials, ensuring...