Clinical Trial Specialist
14 hours ago
Job OverviewWe are seeking a detail oriented Clinical Trial Specialist to support the planning, execution, and management of clinical trials in compliance with regulatory and ethical standards. The role involves coordinating trial activities, maintaining documentation, and ensuring smooth collaboration among internal teams, investigators, and external partners.Key ResponsibilitiesSupport end-to-end clinical trial operations from study start up to close-out.Coordinate with investigators, CROs, and study sites to ensure protocol adherence.Prepare, maintain, and manage essential trial documentation and study files.Assist with site initiation, monitoring, and close-out activities.Track study timelines, milestones, and deliverables.Ensure compliance with ICH-GCP, SOPs, and regulatory requirements.Support IRB/EC submissions, amendments, and approvals.Manage safety reporting, deviations, and issue tracking.Assist in audit and inspection readiness.Support data collection, query resolution, and database lock activities.Required Skills & QualificationsBachelor’s degree in Life Sciences, Pharmacy, or a related field.2+ years of experience in clinical trial operations or clinical research.Strong understanding of clinical trial processes and ICH-GCP guidelines.Experience working with CROs, investigators, and clinical sites.Strong documentation, organizational, and communication skills.Ability to manage multiple studies and priorities effectively.Attention to detail and strong compliance mindset.Tools & Systems (Preferred)Clinical Trial Management Systems (CTMS)Electronic Trial Master File (eTMF) systemsElectronic Data Capture (EDC) systemsMicrosoft Excel, Word, and PowerPointCertifications (Nice to Have)ICH-GCP CertificationClinical Research Coordinator (CRC) certificationClinical Trial Management certificationsWhat We OfferCompetitive compensation and benefitsExposure to global clinical trials and regulatory environmentsOpportunities for career growth in clinical research and operationsCollaborative and compliance-focused work culture
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Clinical Trial Specialist
20 hours ago
bangalore, India TRDFIN Support Services Pvt Ltd Full timeJob Overview We are seeking a detail oriented Clinical Trial Specialist to support the planning, execution, and management of clinical trials in compliance with regulatory and ethical standards. The role involves coordinating trial activities, maintaining documentation, and ensuring smooth collaboration among internal teams, investigators, and external...
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Senior Clinical Trials Professional
19 hours ago
bangalore, India beBeeClinicalTrial Full timeJob Title: Clinical Trial SpecialistWe are seeking a detail oriented professional to support the planning, execution, and management of clinical trials in compliance with regulatory and ethical standards.The role involves coordinating trial activities, maintaining documentation, and ensuring smooth collaboration among internal teams, investigators, and...
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Clinical Quality Assurance Compliance
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bangalore, India Maxis Clinical Sciences Full timeJob Title: Clinical Quality Assurance Compliance & training Experience : 5 plus years Location: Mumbai Type: Full-time Experience Level: (Senior) Manager/Senior Manager Department: Clinical Research Department Purpose of this Role: This role will be responsible for oversight on end-to-end clinical trial activities from quality perspective. This role will be...
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Clinical Trial Compliance Manager
2 weeks ago
bangalore, India beBeeClinicalAudit Full timeClinical Quality Compliance SpecialistEnsure compliance and quality at clinical trial sites through rigorous auditing and monitoring.Responsibilities:Conduct site audits to assess adherence to regulatory requirements and company standards.Review case report forms, informed consent documents, and other regulatory materials.Identify and report audit findings;...
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bangalore, India beBeeOncologist Full timeAs we strive to revolutionize oncology clinical trials, our unified platform eliminates operational inefficiencies in patient recruitment, data curation, and other laborious tasks.The Senior Clinical Data Specialist navigates electronic medical record systems to review clinical trial data for consistency, completeness, and compliance with study protocols and...
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Clinical Trial Manager
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bangalore, India eteraflex connects Full timeCompany Overview: We/eteraflex connects a fast-growing global CRO specializing in oncology, rare diseases, and immunotherapies. Our mission is to accelerate access to innovative treatments by combining regulatory precision with deep site engagement, particularly in complex government-led research environments across India. Position Summary: We are seeking an...
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Bangalore, Karnataka, India Syngene International Full timeJob Location Bangalore Department Clinical Operations About Syngene Incorporated in 1993 Syngene International Ltd is an innovation-focused global discovery development and manufacturing organization providing integrated scientific services to the pharmaceutical biotechnology nutrition animal health consumer goods and specialty chemical industries around the...
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Data Analyst
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bangalore, India beBeeStatisticalProgrammer Full timeJob OverviewThis role is ideal for a skilled statistician who wants to work in clinical trials.ResponsibilitiesMaintain proficiency in statistical programming using SAS.Collaborate with cross-functional teams on trial studies.Analyze and map data to CDISC (SDTM & ADaM) and OMOP standards.Contribute to the validation process using Pinnacle21.Produce...
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Bangalore, Karnataka, India GlaxoSmithKline Full timeBusiness Introduction At GSK we have bold ambitions for patients aiming to positively impact the health of 2 5 billion people by the end of the decade Our R D focuses on discovering and delivering vaccines and medicines combining our understanding of the immune system with cutting-edge technology to transform people s lives GSK fosters a culture ambitious...
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Clinical Operations Manager
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Bangalore, India MS CLINICAL RESEARCH Full timeJob Summary The Clinical Operations Manager will lead and oversee end-to-end clinical study execution across Skin, Hair, and Oral domains. This role is responsible for managing study operations, ensuring compliance with protocols, SOPs, and regulatory guidelines, and coordinating with internal teams, investigators, and sponsors. The candidate will ensure...