Clinical Trial Compliance Specialist
7 days ago
Clinical Quality Compliance Manager Job DescriptionAs a Clinical Site Auditor, you will ensure compliance and quality at Clinical Trial sites. You will conduct site audits, review documentation, and verify adherence to protocols, GCP, GLP, and regulatory requirements.About the Role:This is a key position responsible for ensuring clinical trial sites meet strict regulatory requirements.The successful candidate will be responsible for conducting thorough audits of clinical research sites, reviewing documentation, and verifying compliance with established protocols.Key Responsibilities:Conduct regular audits of clinical research sites across phases I–IV.Review case report forms, informed consent documents, and other regulatory files.Identify and document any non-compliance issues, recommending corrective actions as needed.Provide guidance and training to site staff on compliance procedures.Publish comprehensive audit reports, highlighting areas for improvement and implementing corrective actions.Benefits:This role offers a competitive salary package, opportunities for professional growth and development, and the satisfaction of working in a dynamic healthcare environment.
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Senior Clinical Trial Programming Manager
3 days ago
dombivli, India beBeeStatistical Full timeJob Title: Global Lead Statistical ProgrammerJob DescriptionThis senior-level role leads the programming activities for clinical trials in various therapeutic areas. The successful candidate will be responsible for implementing and executing programming standards to support ongoing studies and requests for study reports, regulatory submissions, and ad...
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Clinical Data Programming Specialist
7 days ago
dombivli, India beBeeDataScientist Full timeSr Statistical Data ScientistWe are seeking an experienced Sr Statistical Data Scientist to support end-to-end clinical data programming activities across multiple studies.This role requires strong technical proficiency, autonomy, and the ability to collaborate effectively within cross-functional teams.Program, validate, and maintain clinical trial datasets...
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Senior Medical Writer
2 weeks ago
Dombivli, India MS CLINICAL RESEARCH Full timeJob Title: Senior Medical Writer Location: MS Clinical Research (MSCR),Department: Medical & Scientific AffairsReporting To: DirectorExperience Required: Minimum 10 years in medical/scientific writingEngagement Type: Consultant – Part-time/Project-based/RemoteRole Summary:MSCR is seeking a highly experienced Senior Medical Writer to oversee the medical...
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Senior Medical Writer
2 weeks ago
Dombivli, India MS CLINICAL RESEARCH Full timeJob Title: Senior Medical Writer Location: MS Clinical Research (MSCR),Department: Medical & Scientific AffairsReporting To: DirectorExperience Required: Minimum 10 years in medical/scientific writingEngagement Type: Consultant – Part-time/Project-based/RemoteRole Summary:MSCR is seeking a highly experienced Senior Medical Writer to oversee the medical...
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Clinical Safety Specialist
7 days ago
dombivli, India beBeeMedical Full timeKey Responsibilities:Perform medical review and clarification of trial-related adverse events (AEs) and post-marketing drug reactions (ADRs)Compose, edit, and medically review analyses of similar events (AOSE) for expedited casesProvide coding review of AEs, SAEs, SADRs, past medical history, concomitant medications, or other medical data...
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Senior Data Analyst
7 days ago
dombivli, India beBeeStatistical Full timeJob Title:Sr. Statistical ProgrammerThe Sr. Statistical Programmer is responsible for programming all tables, listings and graphs necessary for an assigned clinical study report (CSR); developing customized data displays, including data listings, summary tables and routine graphics; writing code using Base SAS programs, SAS procedures or standardized macros;...
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Senior Data Analyst
7 days ago
dombivli, India beBeeStatisticalProgrammer Full timeKey Job ResponsibilitiesDevelop high-quality statistical programming deliverables, including SDTM, ADaM specifications, datasets, reviewer's guide and define.xml files for multiple studies.Create SAS programs that generate datasets, complex listings, tables (including those with descriptive and standard inferential statistics) in collaboration with a...
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Compliance Specialist
3 weeks ago
Dombivli, India Whatjobs IN C2 Full timePayroll & HR Compliance Specialist Key Responsibilities and Deliverables – (India, Singapore, Indonesia, GCC, and Egypt) 1. Regulatory Research & Monitoring Track, interpret, and analyses developments in payroll, employment, social security, and taxation regulations across assigned jurisdictions. Maintain a centralized repository of statutory...
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Clinical Auditor Pharmacist
7 days ago
dombivli, India beBeeAudit Full timePharmacist Role Overview:We are seeking highly skilled and detail-oriented pharmacists in India to support care homes with professional medication auditing, MAR chart reviews, and compliance oversight.This role is ideal for pharmacists with strong analytical skills and a meticulous approach to clinical documentation.Key Responsibilities:Review and audit...
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Dombivli, India VOIS Full timeWe're seeking a dynamic professional for "Hardening Compliance Specialist" role based in Pune. If you're ready to make an impact, this could be the perfect fit!Experience: 6 to 12 yearsLocation: PuneWorking Persona: Hybrid (8 days in a month)Professional Skills/Certifications:ISO2700 LA/LI, CISA, or CISM mandatoryAny other training or certification like...