Clinical Data Management Specialist

About the RoleWe are seeking a highly skilled Global Clinical Data Governance Specialist to join our team at Parexel.

At PSI, we are seeking a highly skilled Lead Clinical Data Manager to join our team.About the RoleThe estimated salary for this position is $85,000 - $110,000 per year, depending on experience and location.Job DescriptionWe are looking for a seasoned professional with expertise in clinical data management to lead our data management activities in large,...

Parexel is seeking a Clinical Data Risk Manager to join our team.The Role:Exemplify and adhere to Parexel values, centering on Collaboration, Agility, Integrity, and Inclusion.Emphasize the importance of process improvement, streamlining processes to add value to our business and meet client needs.Develop and own the Central Monitoring Plan.Contribute to...

Clinical Trials Data SpecialistWe are seeking a skilled Clinical Trials Data Specialist to join our team at Lilly.Key Responsibilities:Collaborate with statistical colleagues and study personnel to provide input to statistical analysis plans.Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding...

About the Role: As a Clinical Trial Specialist at SHA Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd Shanghai Branch, you will play a vital role in ensuring the quality and integrity of our clinical trials. Your primary responsibility will be to oversee all aspects of study site monitoring, including routine monitoring and closeout of...

SHA Fortrea Pharmaceutical Research & Development (Beijing) Co Ltd Shanghai Branch is seeking a highly motivated Clinical Trials Operations Specialist to join our team. The successful candidate will play a critical role in the management and execution of clinical trials, ensuring seamless delivery and compliance with regulatory requirements.About the RoleThe...

The PositionAs a Clinical Utilities Specialist at Roche, you will play a crucial role in creating clinical utilities value and messaging on strategic panels. Your primary focus will be on identifying qualified opportunities for Roche Professional product lines. You will work closely with product managers, supervisors, specialists on disease management...

Job OverviewWe are seeking a seasoned SAS Developer to join our global Data Management team at PSI CRO. The successful candidate will be responsible for delivering high-quality clinical databases and providing expert programming services.About the RoleYou will serve as the primary point of contact for data management and statistics on matters related to...

The Clinical Data Strategy Director will lead the development and execution of the Clinical Data vision, driving growth and sustainability of the customer base. This role requires a deep understanding of the clinical space, clinical data management, and EDC/eClinical applications. The Director will work closely with the sales team to ensure customer success...

At IQVIA, we're pushing the boundaries of human science and data science to create a healthier world. As a Clinical Research Quality Assurance Specialist, you'll be instrumental in ensuring good clinical practices and regulatory requirements are met for assigned clinical studies.Salary: $85,000 - $110,000 per annum (dependent on location and experience)Job...

The Clinical Data Strategy Director will play a pivotal role in driving the growth and adoption of Veeva's Clinical Data solutions across the globe. This individual will be responsible for developing and executing a comprehensive Clinical Data strategy that aligns with the company's vision and goals.About the RoleDevelop and implement a Clinical Data market...

Job DescriptionWe are seeking a highly skilled Senior Clinical Monitoring Specialist to join our team at Fortrea in Xi'an. As a key member of our clinical operations team, you will be responsible for ensuring the successful execution of clinical trials.Key Responsibilities:Monitor study sites independently according to protocol monitoring guidelines, SOPs,...

About the RoleThe Director Clinical Data Strategy position at Veeva Systems is a critical role that requires a deep understanding of the clinical space, clinical data management, and associated EDC/eClinical applications. The ideal candidate will have the ability to drive adoption discussions based on credibility and knowledge across multiple domains,...

Job Description:Key Responsibilities:Develop and implement comprehensive data governance strategies to ensure data quality, security, and compliance.Collaborate with cross-functional teams to design and implement data management solutions that meet business needs.Lead the development of metadata standards and data quality frameworks to improve data accuracy...

Job OverviewWe are seeking a highly skilled Strategic Clinical Utilities Specialist to join our team at Roche.Salary: $120,000 - $180,000 per year, depending on experience and location.Job DescriptionThe successful candidate will be responsible for creating clinical utilities value and messaging on strategic panels, identifying qualified opportunities for...

Job SummaryWe are seeking a highly skilled Clinical Research Specialist to join our Professional Services team in China. As a key member of our team, you will play a crucial role in delivering high-quality EDC study builds, training users, and solving complex challenges in clinical research.

Clinical Study Quality Assurance SpecialistWe are seeking a highly skilled Clinical Study Quality Assurance Specialist to join our team at IQVIA. As a key member of our clinical research team, you will be responsible for ensuring good clinical practices and regulatory requirements are met for assigned clinical studies.Key Responsibilities:Work with Clinical...

Job Summary:As a Clinical Study Manager at Stryker (Beijing) Healthcare Products Co. Ltd - Shanghai Branch, you will play a key role in the successful execution of clinical studies. Your primary responsibility will be to develop and execute clinical project plans, ensuring timely completion and within budget. You will lead a team of clinical staff, providing...

Job SummaryWe are seeking a highly organized and detail-oriented Clinical Trials Specialist to join our team in Shanghai, China. As a key member of our clinical operations team, you will be responsible for ensuring the smooth execution of clinical trials from site initiation to close-out.About the RoleIn this role, you will collaborate with cross-functional...

Job SummaryWe are seeking a highly skilled Global Clinical Research Operations Specialist to join our team at IQVIA. As a key member of our clinical operations department, you will play a crucial role in the planning, execution, and monitoring of clinical trials.