Clinical Trial Specialist
18 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
4 days ago
Bengaluru, India TRDFIN Support Services Pvt Ltd Full timeJob 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...
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Clinical trial specialist
18 hours ago
Bengaluru, India TRDFIN Support Services Pvt Ltd Full timeJob 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...
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Clinical Trial Specialist
4 days ago
Bengaluru, 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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Clinical Trial Specialist
2 days ago
Bengaluru, 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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Clinical Trial Specialist
3 days ago
Bengaluru, Karnataka, India TRDFIN Support Services Pvt Ltd Full timeJob OverviewWe are seeking a detail orientedClinical Trial Specialistto 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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Clinical Trial Coordinator
4 weeks ago
Bengaluru, India ClinoGenesis Research Institute Full timeJob Description – Clinical Trial Coordinator (CTC) | Hyderabad About the RoleThe Clinical Trial Coordinator (CTC) plays a key role in supporting the planning, initiation, execution, and close-out of clinical trials. This role involves coordinating between investigators, clinical research staff, sponsors, and ethics committees to ensure smooth trial...
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Clinical Trial Monitor
3 weeks ago
Bengaluru, India ClinoGenesis Research Institute Full timeClinical Trial Monitor (Entry Level)Role Summary:Assist in clinical trial monitoring activities to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory standards. Support senior CRAs in reviewing data, managing documentation, and coordinating with clinical trial sites.Key Responsibilities:Assist with remote or on-site monitoring...
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Clinical Trial Monitor
3 weeks ago
Bengaluru, India ClinoGenesis Research Institute Full timeClinical Trial Monitor (Entry Level)Role Summary: Assist in clinical trial monitoring activities to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory standards. Support senior CRAs in reviewing data, managing documentation, and coordinating with clinical trial sites.Key Responsibilities:Assist with remote or on-site monitoring...
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Clinical Trial Monitor
3 weeks ago
Bengaluru, India ClinoGenesis Research Institute Full timeClinical Trial Monitor (Entry Level)Role Summary:Assist in clinical trial monitoring activities to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory standards. Support senior CRAs in reviewing data, managing documentation, and coordinating with clinical trial sites.Key Responsibilities:Assist with remote or on-site monitoring...
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Clinical Trial Monitor
3 weeks ago
Bengaluru, India ClinoGenesis Research Institute Full timeClinical Trial Monitor (Entry Level)Role Summary:Assist in clinical trial monitoring activities to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory standards. Support senior CRAs in reviewing data, managing documentation, and coordinating with clinical trial sites.Key Responsibilities:Assist with remote or on-site monitoring...
