Clinical Trials Tester

We are seeking a skilled Clinical Systems Tester to support testing and validation activities in a Decentralized Clinical Trial environment.Key ResponsibilitiesAuthor and execute test scripts aligned with protocol requirementsValidate workflows across eCOA and IRT platforms for DCT toolsCollaborate with clinical ops, data management, and vendors to...

Job Description">As a Clinical Research Associate, you will play a vital role in the execution of clinical trials. You will be responsible for coordinating on-site activities, maintaining essential documents, and supporting the investigator in protocol compliance.The ideal candidate will have a strong background in life sciences, pharmacy, or a related...

Job DescriptionWe are seeking a skilled Clinical Systems Tester to support testing and validation activities within a Decentralized Clinical Trial (DCT) environment.This role requires flexibility across various digital systems and patient-facing technologies, including Veeva CDMS (EDC), eCOA, and IRT platforms.The ideal candidate will have hands-on...

Position :IRT TestersLocation: RemoteDuration : ContractMust have IRT platform experience.INDUSTRY LIFE SCIENCESLOCATION REMOTE (India) reporting to Cambridge, MA 02139INTERVIEW pre-qualifying SPARK HIRE ASSESSMENT and MS TEAMS conversationOVERVIEWWe are looking for a well-rounded Clinical Systems Tester with core expertise in Veeva CDMS (EDC) and strong...

Role Overview:We are seeking a seasoned statistical programmer to lead the development of clinical trials in a fast-paced pharmaceutical environment.This role is ideal for an experienced professional with advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM).The successful candidate will leverage their expertise to support or lead...

We are seeking a seasoned Clinical Research Specialist to spearhead the development of high-quality clinical trial documents. Key responsibilities include crafting protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).Key Responsibilities:Developing comprehensive clinical study...

Job Overview:A senior clinical data coordinator plays a vital role in ensuring the smooth execution of clinical trials by managing and controlling project-specific and departmental documents.Key responsibilities include:Initiating project-specific DMTMF (Data Management Trial Master File) and e-filing processesReviewing and processing Data Clarification...

Key Skills and Qualifications:Hands-on experience with Veeva CDMS (EDC) to author and execute test scripts aligned with protocol requirements.Familiarity with eCOA platforms, such as Medidata, YPrime, and Clinical Ink.Knowledge of IRT systems, including Almac, 4G, and Bioclinica.Prior involvement in DCT environments, including testing for remote or...

Clinical Quality Assurance Specialist Role OverviewThe ideal candidate will provide day-to-day clinical quality assurance support across ongoing clinical trials, ensuring compliance with Good Clinical Practice (GCP) and internal quality standards.Provides QA expertise during study calls, including protocol deviation meetings, risk-based quality management...

Clinical Research Coordinator (Freshers Only)Location: [Insert City or "Across India" if remote/hybrid]Organization: Clinogenesis Research OrganizationDepartment: Clinical operationsType: Full-Time About the Role:Clinogenesis Research Organization is offering an excellent opportunity for fresh graduates to launch their careers as Clinical Research...