Clinical Trials Specialist

Clinical Research Manager OverviewThe Clinical Research Manager plays a pivotal role in leading and overseeing clinical trials and research studies, ensuring timely completion and compliance with regulatory standards.As a senior member of the research team, you will be responsible for managing clinical research projects from start to finish, coordinating and...

Job Overview:Pharmaceutical Data Analyst RoleA pharmaceutical data analyst will collaborate with clients in the pharmaceutical industry, utilizing advanced programming skills and expertise in clinical trials data analysis to support or lead one or more Phase I-IV clinical trials.This role involves manipulating, analyzing, and reporting clinical trial data,...

Senior Statistical Programmer Job DescriptionWe are seeking a skilled Senior Statistical Programmer to support our global pharmaceutical clients in clinical trials.Key Responsibilities:Perform advanced data manipulation, analysis, and reporting using SAS programming.Generate and validate SDTM and ADaM datasets/analysis files, tables, listings, and...

Job DescriptionWe are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in the development and execution of clinical trials.Required Skills and QualificationsAuthor and analyze clinical trial documents.Work with key clinical documents such as protocol, informed consent form,...

Clinical Research Professionals play a vital role in ensuring the success of clinical trials. They assist with on-site coordination, maintain essential documents, and support investigators in protocol compliance.Key ResponsibilitiesAssist with on-site coordination of clinical trial activities under supervisionMaintain essential documents, site files, and...

Job Summary">This role is responsible for overseeing end-to-end clinical trial activities from a quality perspective. The ideal candidate will have 5+ years of experience in Quality Assurance and a strong understanding of GCP guidelines, ICMR regulations, and Drugs and Cosmetic Act requirements.Key ResponsibilitiesDevelop and implement risk-based quality...

About the Position:Develop comprehensive data management strategies to enhance the efficiency and quality of clinical trial data.Design and implement effective data cleaning processes to accelerate subject data cleanliness and ensure timely deliverables.Collaborate with cross-functional teams to guarantee seamless integration with clinical trials, align...

**Job Title: Clinical Systems Tester - Veeva EDC, eCOA, and IRT Platforms**As a skilled Clinical Systems Tester, you will play a pivotal role in ensuring the seamless execution of decentralized clinical trials (DCTs) across various digital systems and patient-facing technologies. This is an exceptional opportunity to leverage your expertise in Veeva CDMS...

Job Overview:We are seeking an experienced Quality Assurance Specialist to provide day-to-day clinical quality assurance support across ongoing clinical trials. This is a dynamic role that requires strong technical skills, effective communication, and a commitment to excellence.The ideal candidate will have a strong foundation in Good Clinical Practice (GCP)...

About Our Clinical Research TeamWe are seeking a highly skilled Medical Writer and Clinical Study Researcher to join our clinical research team. This key role will involve developing high-quality clinical trial documents that support drug development and approval processes.Key Responsibilities:Developing high-quality key clinical trial documents, including...