Clinical Lead for Global Trials

Who we areWere a global midsize CRO that pushes boundaries innovates and invents because the path to a cure for the worlds most persistent diseases is not paved by those who play it safe It is built by those who take pioneering creative approaches and implement them with quality and excellence We are Worldwide Clinical Trials and we are a global team of...

**Driving Success in Clinical Trial Delivery**">Thermo Fisher Scientific is a global leader in the life sciences industry, and we are seeking a highly skilled Project Manager Senior Clinical Trials to join our team. In this role, you will be responsible for the delivery of complex clinical trials, working closely with cross-functional teams to ensure timely,...

Job Description:About the OpportunityThe Senior Clinical Research Manager will provide leadership and oversight to clinical operations staff dealing with centralized trial master files as assigned. This role will be responsible for line management and supervision of DMAs, SDMAs, and CDS, working with all relevant stakeholders within project teams to ensure...

About the RoleWe are looking for a skilled Statistical Programmer who can effectively design and code SAS programs for clinical trials data analysis. The successful candidate will have experience with all SAS language procedures and options commonly used in clinical trial reporting, as well as intermediate knowledge of electronic submissions and CDISC...

About UsInVentiv Health Clinical SRE, LLC is a leading provider of clinical development services. We help pharmaceutical and biotechnology companies bring their products to market by delivering high-quality data and analytics solutions.Our company culture is built on the principles of Total Self, which emphasizes respect, empathy, and inclusivity. We believe...

Job ResponsibilitiesPrimary Liaison: Acts as the primary liaison between InVentiv Health Clinical SRE, LLC and the Customer to ensure project launch, conduct, and closeout according to the Customer's and Company's contractual agreement.Team Leader: Oversees the CDS project team, facilitates team building and communication, and acts as a liaison and...

Job OverviewWe are seeking a highly skilled Technical Lead to join our team at Roche Pharmaceutical Holding. The successful candidate will be responsible for leading the development, optimization, and management of IT services/applications in Veeva with a focus on Clinical Trial Management, Regulatory Information Management, Quality Management, and Quality...

We are seeking a highly skilled Global Clinical Monitoring Expert to join our team. The ideal candidate will have extensive experience in clinical monitoring and site management, with a strong understanding of global regulatory requirements.The Global Clinical Monitoring Expert will be responsible for developing and implementing clinical monitoring plans,...

About Us:We are a leading global clinical research organization (CRO) with a commitment to delivering high-quality services to our clients. With over 29,000 employees across 110 countries, we have a proven track record of success in the pharmaceutical industry. Our company is built on a foundation of collaboration, innovation, and customer satisfaction.We...

Job Overview:The PV Ra Mw Coordinator is a key role in ensuring the smooth execution of clinical trials. As a member of our team, you will provide critical support and coordination in the review of safety and regulatory publishing documents.Responsibilities:Provide critical support and coordination in the review of safety and regulatory publishing...

**Delivering Impactful Results in Clinical Trials**">At Thermo Fisher Scientific, we are seeking a skilled Clinical Project Lead to join our team. As a critical member of our delivery team, you will be responsible for the overall delivery of clinical trials, ensuring quality, time, and cost objectives are met.The successful candidate will have expertise in...

Job type : RemoteShift : US timings3rd Party Data Acquisition Lead (FSP) Role Profile :- Serving as the subject matter expert for the planning, set-up, and acquisition of external clinical data at the study level, managing study start up, conduct and close out activities.- Creating external data transfer agreements, ensuring external clinical trial data are...

Project role : Associate clinical lead Work experiences : 5 to 10 years. Work location : Homebased. Must have skills : Senior Clinical Research associate , CRA, Unblinded Monitoring, Onsite Monitoring. Job overview : Unblinded Clinical Lead working as a oversight for global unblinded CRA team as well as providing technical support for Unblinded...

Project role : Associate clinical lead Work experiences : 5 to 10 years. Work location : Homebased. Must have skills : Senior Clinical Research associate , CRA, Unblinded Monitoring, Onsite Monitoring.Job overview : Unblinded Clinical Lead working as a oversight for global unblinded CRA team as well as providing technical support for Unblinded clinical...

About the RoleThis is an exciting opportunity for a skilled Statistical Programmer to join our team, contributing to the success of our clients through high-quality data analysis and clinical trial support.Key Accountabilities:You will design and implement statistical programs using R, ensuring alignment with regulatory requirements and industry best...

Data Analysis ExpertWe are seeking an experienced professional to join our team as a Data Analysis Expert. In this role, you will work on ADAM and TFL deliverables, creating specifications, and developing utility macros. You will be responsible for developing SDTM and ADaM artifacts, including specifications, datasets, cSDRG, ADRG, and TFLs.Main Objectives-...

About UsNovotech is a leading Asia-Pacific biotech specialist CRO, consisting of two operating brands: Novotech and PPC. With over 3,700 clinical projects completed, including Phase I to Phase IV clinical trials and bioequivalence studies, we are positioned to serve biopharmaceutical clients conducting clinical trials in Asia and globally.We have offices in...

Company OverviewIQVIA is a leading provider of advanced analytics, technology solutions, and human data science expertise focused on driving healthcare forward. With over 60 years of experience in clinical trials, we have a proven track record of delivering high-quality results that drive business growth. Our team of experts is dedicated to helping clients...

Job Description JOB DESCRIPTION Brief Position Description: The core responsibility for this position is as a member of the Data Management department at Novotech. The (Senior) Clinical Data Programmer will be responsible for programming activities on clinical trial projects and to ensure compliance with Good Clinical Data Management Practices...

Job DescriptionJOB DESCRIPTIONBrief Position Description:The core responsibility for this position is as a member of the Data Management department at Novotech. The (Senior) Clinical Data Programmer will be responsible for programming activities on clinical trial projects and to ensure compliance with Good Clinical Data Management Practices (GCDMP).Minimum...