Clinical Trials Specialist

Job Title: Senior BiostatisticianThe primary goal of this position is to provide high-quality statistical expertise and support to clinical trials. This will involve collaborating with cross-functional teams, including Biostatisticians, Statistical Programmers, Clinical Data Managers, and Clinical Research Associates.The Senior Statistician will be...

Senior Statistical ProgrammerJob Description:We are seeking a highly skilled Senior Statistical Programmer to join our team. As a Senior Statistical Programmer, you will be responsible for leading or supporting the development of clinical trial data, including performing data manipulation, analysis and reporting using SAS...

Job Overview:Clinical Research Associates are critical to the success of clinical trials, responsible for authoring and analyzing various documents.Key Responsibilities include:Creating, validating, and refining prompts for AI-assisted document generationEnsuring compliance with global regulatory standards by applying knowledge of clinical trial phases,...

Clinical Systems TesterJob Description:We are looking for a well-rounded Clinical Systems Tester with core expertise in Veeva CDMS (EDC) and strong hands-on experience with eCOA and IRT platforms. This role supports testing and validation activities within a Decentralized Clinical Trial (DCT) environment, requiring flexibility across various digital systems...

Financial Project CoordinatorWe are seeking a Financial Project Coordinator to join our team in supporting the operational project teams financially throughout the life cycle of the project.The ideal candidate will have strong Excel/PC skills and ability to thrive in a multi-tasking environment, with high energy and enthusiasm to exceed expectations. They...

Clinical Systems Tester Job DescriptionOur company is seeking a skilled Clinical Systems Tester to support testing and validation activities within a Decentralized Clinical Trial (DCT) environment.Key Responsibilities:Author and execute test scripts in Veeva EDC, aligned with protocol requirements.Validate workflows across eCOA and IRT platforms.Participate...

Job DescriptionDelhi and Bangalore based opportunity to work on key clinical trial documents, protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).Required Skills & QualificationsProficient in developing high-quality clinical trial documents.Excellent scientific writing skills...

Job Description:We are seeking an experienced and motivated Clinical Research Tutor/Trainer to join our academic team. The candidate will deliver engaging and industry-relevant training in clinical research methodologies, regulatory affairs, pharmacovigilance, and clinical trial operations. The candidate will also contribute to curriculum development,...

Job Title: QA SpecialistKey Responsibilities:Serve as the primary quality assurance support resource for clinical study teams, ensuring compliance with Good Clinical Practice (GCP) and internal quality standards.Provide quality assurance expertise during study calls, including protocol deviation meetings, risk-based quality management discussions, study...

About this RoleWe are seeking a Clinical Data Specialist to take ownership of data management activities for our ongoing clinical studies. This 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 research standards.Key...