Clinical Data Manager

Job OpportunityWe are seeking a Senior Clinical Data Coordinator to join our team. In this role, you will play a crucial part in ensuring the accuracy and quality of clinical data.Main Responsibilities:Data tracking and control activitiesCRF reviews and document verificatione-Filing initiation and project coordinationDocument preparation and update...

**Job Title:** Clinical Data SpecialistAbout the RoleWe are seeking a skilled Clinical Data Specialist to oversee data management activities for our clinical studies. The role requires end-to-end responsibility for data collection, cleaning, storage, quality control, and preparation of datasets for analysis, ensuring accuracy, integrity, and compliance with...

Establish a highly effective clinic leadership role to oversee daily operations, drive revenue growth, and enhance client satisfaction.Key Responsibilities:Manage clinic operations efficiently to guarantee seamless experiences for both staff and clients.Cultivate revenue streams by monitoring sales, setting goals, and collaborating on promotions that...

Job Title: Senior Data Scientist - Clinical Lab ExpertiseWe are seeking a highly skilled Data Scientist to join our team in the role of Senior Data Scientist - Clinical Lab Expertise. In this position, you will be responsible for providing comprehensive clinical lab data expertise as part of a team to develop and maintain Laboratory Data Management (LDM)...

Job Title: Clinical Systems TesterWe are seeking an accomplished professional to join our team as a Clinical Systems Tester. This role is ideal for an individual with experience in Veeva CDMS, eCOA, and IRT platforms.Key Responsibilities:Develop and execute test scripts in Veeva EDC, aligned with protocol requirements.Validate workflows across eCOA and IRT...

We are currently looking for a skilled and experienced Clinical Systems Tester to join our team in the role of Clinical Systems Validation Specialist.Key Responsibilities:Author and execute test scripts in Veeva EDC, aligned with protocol requirements.Validate workflows across eCOA and IRT platforms.Participate in system validation (IQ/OQ/PQ, UAT) for DCT...

Clinical Study Researcher and Medical Writer PositionAbout this position:We are seeking a highly skilled Clinical Study Researcher and Medical Writer to develop high-quality clinical trial documents, translate complex scientific data into clear regulatory compliant documents, and craft abstracts and manuscripts.Key Responsibilities:Developing high-quality...

Clinical Support Specialist RoleOur organization is seeking a skilled Clinical Admin Associate to join our team on a remote basis. The successful candidate will be responsible for managing high-volume clinician/clinic communications, maintaining accurate records, and adhering to strict confidentiality protocols.As a key member of our support team, the...

Key ResponsibilitiesThe primary objective of this role is to provide programming support for clinical trials. This involves delivering exceptional services across the drug development journey, working effectively with other programmers, statisticians, data managers, and database programmers to ensure accurate and high-quality statistical outputs.Exceed...

Job Role OverviewThe Central Monitor II is a key professional responsible for ensuring the quality and integrity of clinical trial data through centralized monitoring activities, statistical data review, and proactive risk management.Main ResponsibilitiesConduct thorough risk assessments for clinical studies, identifying potential issues and developing...