Senior Clinical Trial Compliance Officer

2 weeks ago

ajmer, India beBeeClinicalAudit Full time

Quality Assurance SpecialistJob Summary:As a Quality Assurance Specialist, you will be responsible for ensuring the quality and compliance of clinical trial sites by conducting audits, reviewing documents, and verifying adherence to protocols and regulations.Key Responsibilities:Conduct thorough audits of clinical research sites across phases I–IV, ensuring that all necessary procedures are followed.Review and assess CRFs, informed consent forms, and regulatory documents to ensure accuracy and completeness.Identify and report any audit findings, recommending corrective actions to site staff.Provide guidance and training to site staff on compliance matters, promoting a culture of excellence and integrity.Prepare detailed audit reports, summarizing key findings and recommendations for CAPA implementation.Requirements:Proven experience in quality assurance or a related field, with a strong background in auditing and regulatory compliance.Excellent analytical and problem-solving skills, with the ability to identify and address complex issues.Strong communication and interpersonal skills, with the ability to work effectively with site staff and other stakeholders.Ability to travel as required, with flexibility to accommodate remote and field work arrangements.Benefits:Competitive salary and benefits package.Opportunities for professional growth and development.Collaborative and dynamic work environment.Travel Requirements:Travel required for site audits and other business needs.

  • Senior Statistical Lead

    2 weeks ago

    ajmer, India beBeeStatistical Full time

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  • Lead Data Scientist

    1 week ago

    ajmer, India beBeeStatistical Full time

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    Ajmer, India Clinovo Full time

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  • Clinical Research Site Auditor

    1 week ago

    ajmer, India beBeeClinicalResearch Full time

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  • Expert Clinical Data Manager

    4 days ago

    ajmer, India beBeeClinicalDataManager Full time

    Job DescriptionAs an Expert Clinical Data Manager, you will be responsible for the setup and management of clinical trials on our electronic data capture (EDC) system. This involves designing, developing, and validating eCRF specifications to ensure seamless trial execution.Create edit check specifications and set up edit checks at the trial level to ensure...

  • Senior Data Analyst

    2 days ago

    ajmer, India beBeeDataScientist Full time

    Statistical ProgrammerWe are seeking a detail-oriented and highly organized Statistical Programmer to join our team.This role involves developing, validating and maintaining ADaM datasets, TLFs and other analytical outputs for clinical trials.The successful candidate will support Oncology studies by ensuring accuracy, consistency and regulatory compliance in...

  • Senior Compliance Officer

    1 week ago

    ajmer, India beBeeCompliance Full time

    Job Title: Senior Compliance OfficerWe are seeking a seasoned professional to join our team as a Senior Compliance Officer. This role will be responsible for ensuring that all business activities are in compliance with relevant laws and regulations.The ideal candidate will have a strong background in compliance, risk management, or regulatory affairs, with...

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    1 week ago

    ajmer, India beBeeStatistical Full time

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  • Senior Compliance Officer

    2 weeks ago

    ajmer, India beBeeCompliance Full time

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  • Expert Data Analyst

    4 days ago

    ajmer, India beBeeR Full time

    Senior Programmer Role OverviewThis senior programmer position is ideal for candidates with a strong background in R programming and data analysis. The successful applicant will have experience working with clinical trial data, CDISC ADaM and SDTM standards, and industry R packages such as ADMIRAL and OAK.