Clinical Compliance Specialist
1 week ago
Key Roles:Conduct comprehensive site audits to ensure compliance and quality at clinical trial sites.Review CRFs, informed consent forms, and regulatory documents to identify audit findings.Provide guidance and training to site staff on compliance and protocol adherence.Prepare detailed audit reports and follow up on CAPA implementation.Requirements:10-12 years of experience in clinical research with a focus on auditing and QA.Strong communication, analytical, and organizational skills.Able to travel extensively for site audits.Preferred qualifications include certification in Clinical Research or Quality Auditing (ACRP, SOCRA).Experience with eTMF and EDC systems is also desirable.Working Conditions:Up to 50% travel to clinical sites.Combination of remote and field work.
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Clinical Research Compliance Specialist
1 week ago
india beBeeClinical Full timeJob Title: Clinical Research Compliance SpecialistClinical Research Compliance Specialists play a critical role in ensuring the integrity and quality of clinical trials.Key Responsibilities:Conduct thorough audits of clinical research sites to ensure compliance with regulatory requirements and site policies.Review and verify documentation, including CRFs,...
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Clinical Quality Assurance Compliance
1 week ago
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 Quality Assurance Compliance
2 weeks ago
Mumbai, Maharashtra, India, Maharashtra Maxis Clinical Sciences Full timeJob Title: Clinical Quality Assurance Compliance & trainingExperience: 5 plus yearsLocation: MumbaiType: Full-timeExperience Level: [Senior] Manager/Senior ManagerDepartment: 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 Compliance Specialist
6 days ago
india beBeeAuditor Full timeJob Title: Clinical Quality Compliance ManagerClinical Site Auditor to 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.Key Responsibilities:Conduct site visits of clinical research sites across phases I–IV.Review case report...
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Clinical Research Coordinator
1 week ago
Junagadh, India Triethix Clinical Research SMO Full timeJob Description Company Description Triethix Clinical Research is a clinician-led Site Management Organization (SMO) based in Ahmedabad, India, specializing in efficient and compliant execution of clinical trials. Focused on optimizing trial site operations, Triethix collaborates with CROs, sponsors, and investigators to deliver expertise in site...
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Manager, Quality Trust and Compliance
7 hours ago
Itanagar, India Endpoint Clinical Full timeJob Description About Us Endpoint is an interactive response technology (IRT) systems and solutions provider that supports the life sciences industry. Since 2009, we have been working with a single vision in mind, to help sponsors and pharmaceutical companies achieve clinical trial success. Our solutions, realized through the proprietary PULSE platform, have...
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Clinical Operations Manager
2 weeks ago
Bengaluru, Karnataka, India, Karnataka MS CLINICAL RESEARCH Full timeJob SummaryThe 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...
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Clinical Specialist
1 day ago
New Delhi, India (INNWD, ., H) IQVIA Full timeClinical Specialist / Stroke Rater – Punjabi SpeakingLocation: RemoteHours: Estimated 2–12 hours per month, flexibleRole OverviewThe Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality and consistency. This includes rating patients using validated stroke scales and reviewing assessments...
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Clinical Specialist
1 day ago
New Delhi, India (INNWD, ., H) IQVIA Full timeClinical Specialist / Stroke Rater – Gujarati SpeakingLocation: RemoteHours: Estimated 2–12 hours per month, flexibleRole OverviewThe Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality and consistency. This includes rating patients using validated stroke scales and reviewing assessments...
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Clinical Research Manager
2 weeks ago
India Chartered Institute of Professional Certifications Full timeJob Description About Us The Chartered Institute of Professional Certifications is a global leader in executive education and industry-recognized certification programs. We collaborate with distinguished faculty, regulatory experts, and research leaders to deliver world-class training across clinical trials, pharmaceuticals, healthcare compliance, medical...