Inpatient Clinical Documentation Integrity

About the Role: We are seeking a seasoned and detail-oriented Inpatient CDI Specialist to improve clinical documentation accuracy and align it with inpatient coding standards. This role emphasizes enhancing data quality, ensuring proper risk adjustment, and maintaining compliance to support organizational quality and financial objectives. Key...

Job DescriptionWe are seeking a highly skilled Senior Regulatory Specialist to lead our regulatory team in preparing and maintaining complete and accurate regulatory documents in support of clinical research studies. As a subject matter expert and leader, you will be responsible for ensuring regulatory submissions are done in a timely manner to avoid delays...

Job SummaryBristol-Myers Squibb is seeking a highly skilled Clinical Documentation Specialist to join our team. In this role, you will be responsible for managing and executing centralized activities in support of global trials with an emphasis on clinical documentation.About UsWe are a leading biopharmaceutical company dedicated to transforming patients'...

Transforming Patients' Lives Through ScienceBristol Myers Squibb is committed to delivering innovative solutions that improve patient outcomes. As a Quality Assurance Specialist, you will be an integral part of our team, ensuring the accuracy and consistency of clinical and regulatory documents.Key ResponsibilitiesIn this role, you will be responsible...

Job Overview:Staffingly, Inc. is dedicated to helping healthcare providers deliver better, faster, and more accurate care. We are seeking a highly skilled Clinical Documentation Expert to join our onsite team in Hyderabad. In this role, you will be responsible for ensuring the accuracy and quality of clinical documentation.Your Key Responsibilities:Ensure...

**About the Role**We are seeking a talented Clinical Documentation Specialist to join our team at Hetero. In this role, you will be responsible for developing and reviewing clinical documents, including protocols, investigator's brochures, case record forms, product rationales, prescribing information, drug interactions, and clinical study reports.**Key...

This job is with Novartis, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Summary Clinical Document Governance Management (CDGM) is accountable for...

Job Description">Hetero seeks a highly skilled Clinical Document Specialist to join our team. In this role, you will be responsible for developing and reviewing clinical documents, including protocols, investigator brochures, case record forms, product rationales, prescribing information, drug interactions, and clinical study reports.">Key...

About the JobThis role involves leading a regulatory team to prepare and maintain regulatory documents for clinical research studies. The ideal candidate will have strong leadership skills and experience in clinical research regulation.Responsibilities:Supervise regulatory specialists supporting multiple Velocity Clinical Research sitesReview and submit...

Job OverviewBristol-Myers Squibb is a leading pharmaceutical company dedicated to transforming patients' lives through science. As a Clinical Document Review Specialist, you will play a critical role in ensuring the quality of clinical and regulatory documents.ResponsibilitiesCritically review complex clinical documents for timely submission to health...

About Velocity Clinical Research, Inc.Velocity Clinical Research, Inc. is a leading research site organization that provides exceptional patient care, high-quality data, and fully integrated research sites. Our mission is to bring innovative medical treatments to patients by generating high-quality data from as many patients as possible, as quickly as...

About the RoleThis is a critical position within our organization, requiring strong expertise in medical writing and regulatory compliance. The successful candidate will have excellent communication and project management skills, with the ability to work effectively in a fast-paced environment.Key Responsibilities:- Develop and review clinical documents,...

Job Description:The role of Technical Architect – System Integration (Clinical & Pharma Systems) at Capgemini Engineering involves designing and implementing integration solutions for clinical and pharma systems. A key aspect is ensuring interoperability using standards such as HL7, FHIR, CDISC, and others.Key Responsibilities:- Design and implement...

Job Description:The Senior Regulatory Specialist is responsible for leading a team of regulatory specialists in preparing and submitting regulatory documents in support of clinical research studies. This includes ensuring timely completion of regulatory submissions, preparing study-specific protocol, informed consent form, HIPAA authorization, and other...

About the Role">We are seeking a highly skilled Clinical Documentation Expert to join our team at Amgen.">The successful candidate will have a strong background in scientific or medical knowledge, with the ability to understand and comply with SOPs, templates, best practices, policies, and Regulatory Writing Style Guides.">This role involves compiling and...

About the jobAbout SukoonSukoon Health is building India's first specialized chain of hospitals to cater to acute and severe mental health conditions.We plan to set up 1000 beds across 40 units for adult, acute inpatient care across India. Additionally, we have aspirations to expand into specialized segments of de-addiction, child development disabilities,...

We are seeking a highly organized and detail-oriented Global Document Manager to join our Clinical Development team at Bristol-Myers Squibb. In this role, you will be responsible for managing and executing start-up documentation activities for global clinical trials, developing and maintaining collaborative working relationships with clinical investigator...

Job OverviewWe are seeking a Senior Regulatory Specialist to join our team at Velocity Clinical Research, Inc. As a member of our regulatory team, you will play a critical role in ensuring the success of our clinical research studies by preparing and maintaining complete and accurate regulatory documents.As a subject matter expert and leader, you will be...

About Sukoon HealthSukoon Health is pioneering India's first specialized chain of hospitals focused on treating acute and severe mental health conditions. Our goal is to establish a network of 40 units with 1000 beds, offering adult, acute inpatient care across the country. We also aspire to expand into de-addiction, child development disabilities, dementia...

Dear Candidates,Looking for coder opening for surgery,EXL and E/M.Min - 3 yearsCtc for coder - 9 lakhs - 12 lakhsquality and AM Lead - 13 lakhs - 15 lakhsAny certification is mandatory.Contact Details: Reach me out Priya Hr (6381133167) or share me ( mohanapriya@covenantindia.net )Job Title: IP-DRG, Surgery, and E/M CoderLocation: [Insert...