Skill required: Clinical Data Services - Clinical Database Programming Designation: Sr. Clinical Data Programming Associate Qualifications:BCA Years of Experience:3- 5 Yrs About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and
Skill required: Clinical Data Services - Clinical Database Programming Designation: Sr. Clinical Data Programming Scientist Qualifications:BE,BTech Years of Experience:7 to 11 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience
Skill required: Clinical Data Services - Clinical Reports Management Designation: Sr. Clinical Data Programming Scientist Qualifications:BE,BTech Years of Experience:7 to 11 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched
Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries through Catalyst Oncology, a full-service oncology CRO,andmulti-therapeutic global functional and CRO services through Catalyst Flex. The companys customer-centric flexible service model, innovative technology, expert team
Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Specialist Qualifications:BE Years of Experience:7 to 11 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience
At Allucent, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe. The Senior Clinical Programmer I (SrCP1) develops and coordinates
About the Role: The CDP-II is responsible for the design, development, programming, validation, and maintenance of clinical trial databases throughout the study lifecycle. This includes clinical database build, Case Report Form (CRF) design, edit check programming, custom function development, external
About the Role: The Clinical Programmer (SDTM) is primarily responsible for SDTM programming based on Clinical Protocols, eCRF and Statistical Analysis Plans. The Clinical Programmer (SDTM) may also be responsible for data submission packages to clients and regulators. The Clinical Programmer
Work ScheduleSecond Shift (Afternoons) Environmental ConditionsOffice Job Description Join us as a Director Programming, make an Impact at the Forefront of Innovation Summary: The Director Programming provides operational leadership for the bioinformatics programming function. The role involves evaluating workloads,
Work Flexibility: Hybrid Job Summary This position is responsible for providing statistical guidance in development of clinical research programs and of individual studies as part of multi-disciplinary team. This role involves the development of Statistical Analysis Plans,
Position Summary: The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard
Position Summary: The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as a Manager Clinical Data Managemnet Programming - Make an Impact at the Forefront of Innovation The Manager Clinical Data Managemnet Programming oversees the day-to-day operations for the team and the resources
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical development
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical development
When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every clinical development
Senior Clinical Python Programmer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at
Career CategoryClinical Development Job Description Sr Associate Biostatistical Programming The Biostatistical Programming Senior Associate will work in Amgens Global Randomization and Blinding (GRB) organization Responsibilities include: Creating and delivering Participant and Investigational Product (IP) randomization lists meeting specifications
Job Overview Manage end-to-end delivery of data management services for single/multi-service projects with minimal guidance, ensuring quality deliverables on time and within budget, to customer satisfaction. Provide comprehensive data management expertise to Data Management (DM) team
About the role: The Team Lead Data Management will have responsibility for Data Management staff as assigned and ensures that line reports conduct clinical trials according to all applicable Good Clinical Practice (GCP), Regulatory Requirements, Standard Operating Procedures