Clinical Trials Coordinator I

About UsBEJ Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd is a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience.Company OverviewWe provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and...

Job Summary: We are seeking a highly organized and detail-oriented Clinical Trials Administrator to join our team at BEJ Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd. The successful candidate will be responsible for providing administrative support to our clinical trials team, ensuring the smooth execution of studies and maintaining...

Unlocking Success in Clinical ResearchOur team at Parexel is dedicated to delivering exceptional results in clinical trials. As a Clinical Research Associate I(FSP), you will play a critical role in ensuring the success of our studies.Key Responsibilities:Source Data Verification and Data Management Conduct thorough source data verification and ensure timely...

Job Title: Clinical Research Associate IAbout the Role:Parexel is seeking a highly motivated and detail-oriented Clinical Research Associate I to join our team. As a Clinical Research Associate I, you will be responsible for managing clinical trials from site identification through close-out, ensuring timely and accurate completion of project goals.Key...

Job SummaryWe are seeking a highly organized and detail-oriented Clinical Trials Administrator to join our team at BEJ Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd. As a Clinical Trials Administrator, you will play a critical role in the success of our clinical trials by providing administrative support to our project teams.Key...

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...

Job Title: Clinical Research Associate IAt Parexel, we are seeking a highly skilled and motivated Clinical Research Associate I to join our team. As a Clinical Research Associate I, you will play a critical role in the success of our clinical trials by ensuring the integrity and quality of our research.Key Responsibilities:Act as Parexel's direct point of...

Job Title: Clinical Research Associate IParexel is seeking a highly motivated and detail-oriented Clinical Research Associate I to join our team. As a Clinical Research Associate I, you will be responsible for ensuring the integrity and quality of clinical trials from site identification to close-out.Key Responsibilities:Act as Parexel's direct point of...

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 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...

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...

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...

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...

Job Summary: We are seeking a skilled Clinical Research Associate I (FSP) to join our team at Parexel.About the Role:Conduct Source Data Verification and Ensure Clinical Trials Data are Submitted in a Timely Fashion: The successful candidate will be responsible for conducting source data verification (SDV) and ensuring that clinical trials data are submitted...

Company Overview:SHA Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd Shanghai Branch is a dynamic and innovative company that is revolutionizing the development process of clinical trials. Our commitment to delivering life-changing ideas and therapies to patients in need drives us to seek motivated problem-solvers and creative thinkers who...

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...

**Job Overview**At IQVIA, we are seeking a highly organized and detail-oriented Clinical Research Coordinator to support our clinical research operations team. The successful candidate will assist in the preparation, handling, distribution, and archiving of clinical documentation and reports, ensuring compliance with standard operating procedures.**Key...