497 Clinical Documentation jobs in India
Freelance Medical Writer
Job Viewed
Job Description
Job Summary:
We are seeking a highly skilled Medical Content Production Individual accountable for content creation of medical publications and communications. The ideal candidate will have proven expertise in medical writing, planning and strategy in the pharmaceutical industry. Candidate will be closely working with peer writers and will be responsible for the training of the team.
Key Responsibilities:
- Able to conduct literature searches (PubMed, EMBASE, clinicaltrial.gov, EudraCT, congresses, COCHRANE), screening, data extraction, and analysis to support content development.
- Independently compiles, writes, and edits medical writing deliverables including operating guidance documents, SOPs, training guides, etc.
- Develops research articles (primary/secondary), review articles, case reports, editorials, perspectives, short communications, abstracts, posters, oral presentations, visual abstracts, publication cards (static/interactive/video), publication summaries, and publication extenders.
- Works with team to produce high quality clinical regulatory documents (Clinical Study Protocols, Clinical Study Reports, Clinical Summaries in the CTD format, Investigator Brochures, IMPDs/INDs, scientific publications) as the lead writer.
- Guides team for requirements (keywords, analysis), creates structured data extraction forms, and able to lead systematic review.
- Prepares emailers/e-Blasts, microsite, flip books, booth materials such as flyers, bag inserts, roll-up banners (print/digital).
- Congress session coverage (daily highlights, training slides) and KOL interviews.
- Creates scientific slide decks, infographics, newsletters/news highlights.
- Supports ad boards, symposiums, webinars, standalone events with briefing slides and meeting materials.
- Develop podcasts, audio/video articles, animations, insights reports, and KOL profiling/mapping.
- Able to interpret the statistical data.
- Proof-reading and typesetting checks including correctness of font and symbols; text and image clarity/visibility; aesthetics (alignment, layout, consistency); formatting, spacing.
- Formatting documents based on journal/congress guidelines.
- Ensuring that the document adheres to specified style guides – AMA/APA/Vancouver Manual of Style/brand style/Client Guidelines.
- Adheres to established regulatory standards as well as Company Standard Operating Procedures, client standards, brand guidelines, and Company and/or client approved templates when completing medical writing projects, on-time and on-budget.
- Additionally, candidate will be expected to prepare the SOPs and training materials for the team.
Required Skills & Qualifications:
- Education :
- B.Sc./M.Sc./PhD/MD in life sciences/pharmacy or related field.
- Experience :
- 5-10 years of experience in medical writing or scientific communications within the pharmaceutical industry.
- Proven track record of creating high-quality publications.
- Produced systematic reviews.
- Technical Skills :
- Adobe Suite, VEEVA PromoMats, EndNote, ZOTERO, Mendeley.
- Literature searches (NCBI, Cochrane, EMBASE, EudraCT, MEDLINE).
- Understands HTA (Health Technology Assessment) guidelines.
- Familiarity with EMA, FDA, NICE, and WHO evidence requirements.
- Systematic review tools (e.g., Covidence, Rayyan, DistillerSR).
- Systematic review methodologies.
- Soft Skills :
- Strong project management skills with the ability to handle multiple tasks under tight deadlines.
- Excellent communication skills to collaborate with cross-functional teams (medical affairs, marketing).
- Attention to detail with a strong focus on scientific accuracy and compliance.
- Languages : Excellent knowledge of the English language (spoken and written).
Good to have :
- Publication planning & strategy.
- Statistical analysis knowledge.
- Basic understanding of graphic tools.
- Certification in medical writing, pharmaceutical communications, Gen AI is a plus.
- Demonstrated ability to work with tight timelines and a collaborative environment
- The ideal candidate is self-motivated and process-driven but able to deal with rapid change in a fast- paced, deadline-driven environment
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Clinical Documentation Improvement Specialist (CDI)
Posted 5 days ago
Job Viewed
Job Description
Thryve Digital Health LLP is an emerging global healthcare partner that delivers strategic innovation, expertise, and flexibility to its healthcare partners. Being a US healthcare conglomerate captive, we have direct access to deeper insights that help us accelerate our learning process and keeps us ahead of the curve. Thryve delivers next-generation solutions that enable our healthcare partners to provide positive experiences to their consumers.
Our global collaborative of healthcare, operations, and IT experts creates innovative and sustainable processes for our clients, which keeps the ever-evolving consumers engaged and assists them in managing the future of their healthcare better. We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. Thryve is an equal opportunity employer and places a high value on integrity, diversity, and inclusion in the organization. We do not discriminate on the basis of any protected attribute. For more information about the organization, please visit
Job Title: Senior Clinical Documentation Improvement (CDI) Specialist
Department: Revenue Cycle Management/Clinical Documentation Improvement
Reports To: CDI Manager/Director
Location: Chennai/Hyderabad
Summary:
The Senior CDI Specialist is responsible for leading clinical documentation improvement efforts to ensure accurate and complete medical record documentation that supports appropriate coding, reimbursement, and quality reporting. This role requires expertise in clinical documentation requirements, coding guidelines, and regulatory standards. The Senior CDI Specialist performs comprehensive medical record reviews, collaborates with physicians and other healthcare providers, provides education and training, and serves as a resource for the CDI team.
Key Responsibilities:
Medical Record Review:
- Conduct concurrent and retrospective reviews of inpatient and outpatient medical records to identify opportunities for documentation improvement.
- Evaluate the accuracy and completeness of clinical documentation to ensure it reflects the patient's condition, treatment, and outcomes.
- Identify discrepancies, inconsistencies, and missing information in the medical record.
- Analyze documentation to determine the principal diagnosis, comorbidities, and complications.
Physician Collaboration and Education:
- Communicate with physicians and other healthcare providers to clarify documentation and obtain additional information.
- Provide education and training to physicians and other healthcare providers on documentation requirements, coding guidelines, and regulatory standards.
- Conduct one-on-one education sessions with physicians to address specific documentation deficiencies.
- Develop and deliver educational materials, presentations, and workshops on CDI topics.
Coding and Reimbursement:
- Ensure that documentation supports accurate coding and billing practices.
- Collaborate with coding staff to resolve coding discrepancies and documentation issues.
- Understand the impact of documentation on reimbursement and DRG (Diagnosis Related Group) assignment.
- Stay current on changes in coding guidelines (ICD-10, CPT, HCPCS) and reimbursement policies.
Data Analysis and Reporting:
- Collect and analyze data related to CDI activities, including query rates, physician response rates, and documentation improvement metrics.
- Prepare reports and presentations on CDI performance and trends. Identify opportunities to improve CDI processes and outcomes.
- Participate in quality improvement initiatives and performance improvement projects.
Regulatory Compliance:
- Ensure compliance with all applicable regulatory requirements, including HIPAA, CMS (Centers for Medicare & Medicaid Services), and Joint Commission standards.
- Stay current on changes in regulatory requirements and guidelines related to clinical documentation and coding.
- Participate in internal audits and external reviews of clinical documentation.
Team Leadership and Mentorship:
- Serve as a mentor and resource for junior CDI Specialists.
- Provide guidance and support to the CDI team on complex cases and documentation challenges.
- Assist in training new team members on CDI processes and procedures.
- Participate in team meetings and contribute to the development of CDI strategies.
System Proficiency:
- Utilize electronic health record (EHR) systems and CDI software to manage medical record reviews and documentation queries.
- Maintain accurate and up-to-date information in CDI tracking systems.
Qualifications, Experience & Skills:
- Registered Nurse (RN), Certified Coding Specialist (CCS), Certified Clinical Documentation Specialist (CCDS), or other relevant clinical or coding certification required.
- Bachelor’s degree in science, Pharma, Nursing, Health Information Management, or a related field preferred.
- Minimum of 5-7 years of experience in clinical documentation improvement, coding, or related healthcare field.
- Strong knowledge of medical terminology, anatomy and physiology, and disease processes.
- Experience working with electronic health record (EHR) systems.
- Excellent communication and interpersonal skills.
- Strong analytical and problem-solving abilities.
- Ability to work independently and as part of a team.
- Excellent organizational and time-management skills.
- Proficiency in using Microsoft Office Suite.
Certifications:
- Required: RN, CCS, CCDS, or other relevant clinical or coding certification.
- Experience with EPIC preferred but not mandatory
- Both Hospital and Professional CDI experience preferred
- Flexible to work from Office all 5 days in the week
Clinical Documentation Improvement Specialist (CDI)
Posted 1 day ago
Job Viewed
Job Description
Thryve Digital Health LLP is an emerging global healthcare partner that delivers strategic innovation, expertise, and flexibility to its healthcare partners. Being a US healthcare conglomerate captive, we have direct access to deeper insights that help us accelerate our learning process and keeps us ahead of the curve. Thryve delivers next-generation solutions that enable our healthcare partners to provide positive experiences to their consumers.
Our global collaborative of healthcare, operations, and IT experts creates innovative and sustainable processes for our clients, which keeps the ever-evolving consumers engaged and assists them in managing the future of their healthcare better. We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. Thryve is an equal opportunity employer and places a high value on integrity, diversity, and inclusion in the organization. We do not discriminate on the basis of any protected attribute. For more information about the organization, please visit
Job Title: Senior Clinical Documentation Improvement (CDI) Specialist
Department: Revenue Cycle Management/Clinical Documentation Improvement
Reports To: CDI Manager/Director
Location: Chennai/Hyderabad
Summary:
The Senior CDI Specialist is responsible for leading clinical documentation improvement efforts to ensure accurate and complete medical record documentation that supports appropriate coding, reimbursement, and quality reporting. This role requires expertise in clinical documentation requirements, coding guidelines, and regulatory standards. The Senior CDI Specialist performs comprehensive medical record reviews, collaborates with physicians and other healthcare providers, provides education and training, and serves as a resource for the CDI team.
Key Responsibilities:
Medical Record Review:
- Conduct concurrent and retrospective reviews of inpatient and outpatient medical records to identify opportunities for documentation improvement.
- Evaluate the accuracy and completeness of clinical documentation to ensure it reflects the patient's condition, treatment, and outcomes.
- Identify discrepancies, inconsistencies, and missing information in the medical record.
- Analyze documentation to determine the principal diagnosis, comorbidities, and complications.
Physician Collaboration and Education:
- Communicate with physicians and other healthcare providers to clarify documentation and obtain additional information.
- Provide education and training to physicians and other healthcare providers on documentation requirements, coding guidelines, and regulatory standards.
- Conduct one-on-one education sessions with physicians to address specific documentation deficiencies.
- Develop and deliver educational materials, presentations, and workshops on CDI topics.
Coding and Reimbursement:
- Ensure that documentation supports accurate coding and billing practices.
- Collaborate with coding staff to resolve coding discrepancies and documentation issues.
- Understand the impact of documentation on reimbursement and DRG (Diagnosis Related Group) assignment.
- Stay current on changes in coding guidelines (ICD-10, CPT, HCPCS) and reimbursement policies.
Data Analysis and Reporting:
- Collect and analyze data related to CDI activities, including query rates, physician response rates, and documentation improvement metrics.
- Prepare reports and presentations on CDI performance and trends. Identify opportunities to improve CDI processes and outcomes.
- Participate in quality improvement initiatives and performance improvement projects.
Regulatory Compliance:
- Ensure compliance with all applicable regulatory requirements, including HIPAA, CMS (Centers for Medicare & Medicaid Services), and Joint Commission standards.
- Stay current on changes in regulatory requirements and guidelines related to clinical documentation and coding.
- Participate in internal audits and external reviews of clinical documentation.
Team Leadership and Mentorship:
- Serve as a mentor and resource for junior CDI Specialists.
- Provide guidance and support to the CDI team on complex cases and documentation challenges.
- Assist in training new team members on CDI processes and procedures.
- Participate in team meetings and contribute to the development of CDI strategies.
System Proficiency:
- Utilize electronic health record (EHR) systems and CDI software to manage medical record reviews and documentation queries.
- Maintain accurate and up-to-date information in CDI tracking systems.
Qualifications, Experience & Skills:
- Registered Nurse (RN), Certified Coding Specialist (CCS), Certified Clinical Documentation Specialist (CCDS), or other relevant clinical or coding certification required.
- Bachelor’s degree in science, Pharma, Nursing, Health Information Management, or a related field preferred.
- Minimum of 5-7 years of experience in clinical documentation improvement, coding, or related healthcare field.
- Strong knowledge of medical terminology, anatomy and physiology, and disease processes.
- Experience working with electronic health record (EHR) systems.
- Excellent communication and interpersonal skills.
- Strong analytical and problem-solving abilities.
- Ability to work independently and as part of a team.
- Excellent organizational and time-management skills.
- Proficiency in using Microsoft Office Suite.
Certifications:
- Required: RN, CCS, CCDS, or other relevant clinical or coding certification.
- Experience with EPIC preferred but not mandatory
- Both Hospital and Professional CDI experience preferred
- Flexible to work from Office all 5 days in the week
Clinical Documentation Improvement Specialist (CDI)
Posted 5 days ago
Job Viewed
Job Description
Our global collaborative of healthcare, operations, and IT experts creates innovative and sustainable processes for our clients, which keeps the ever-evolving consumers engaged and assists them in managing the future of their healthcare better. We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. Thryve is an equal opportunity employer and places a high value on integrity, diversity, and inclusion in the organization. We do not discriminate on the basis of any protected attribute. For more information about the organization, please visit Title: Senior Clinical Documentation Improvement (CDI) Specialist
Department: Revenue Cycle Management/Clinical Documentation Improvement
Reports To: CDI Manager/Director
Location: Chennai/Hyderabad
Summary:
The Senior CDI Specialist is responsible for leading clinical documentation improvement efforts to ensure accurate and complete medical record documentation that supports appropriate coding, reimbursement, and quality reporting. This role requires expertise in clinical documentation requirements, coding guidelines, and regulatory standards. The Senior CDI Specialist performs comprehensive medical record reviews, collaborates with physicians and other healthcare providers, provides education and training, and serves as a resource for the CDI team.
Key Responsibilities:
Medical Record Review:
Conduct concurrent and retrospective reviews of inpatient and outpatient medical records to identify opportunities for documentation improvement.
Evaluate the accuracy and completeness of clinical documentation to ensure it reflects the patient's condition, treatment, and outcomes.
Identify discrepancies, inconsistencies, and missing information in the medical record.
Analyze documentation to determine the principal diagnosis, comorbidities, and complications.
Physician Collaboration and Education:
Communicate with physicians and other healthcare providers to clarify documentation and obtain additional information.
Provide education and training to physicians and other healthcare providers on documentation requirements, coding guidelines, and regulatory standards.
Conduct one-on-one education sessions with physicians to address specific documentation deficiencies.
Develop and deliver educational materials, presentations, and workshops on CDI topics.
Coding and Reimbursement:
Ensure that documentation supports accurate coding and billing practices.
Collaborate with coding staff to resolve coding discrepancies and documentation issues.
Understand the impact of documentation on reimbursement and DRG (Diagnosis Related Group) assignment.
Stay current on changes in coding guidelines (ICD-10, CPT, HCPCS) and reimbursement policies.
Data Analysis and Reporting:
Collect and analyze data related to CDI activities, including query rates, physician response rates, and documentation improvement metrics.
Prepare reports and presentations on CDI performance and trends. Identify opportunities to improve CDI processes and outcomes.
Participate in quality improvement initiatives and performance improvement projects.
Regulatory Compliance:
Ensure compliance with all applicable regulatory requirements, including HIPAA, CMS (Centers for Medicare & Medicaid Services), and Joint Commission standards.
Stay current on changes in regulatory requirements and guidelines related to clinical documentation and coding.
Participate in internal audits and external reviews of clinical documentation.
Team Leadership and Mentorship:
Serve as a mentor and resource for junior CDI Specialists.
Provide guidance and support to the CDI team on complex cases and documentation challenges.
Assist in training new team members on CDI processes and procedures.
Participate in team meetings and contribute to the development of CDI strategies.
System Proficiency:
Utilize electronic health record (EHR) systems and CDI software to manage medical record reviews and documentation queries.
Maintain accurate and up-to-date information in CDI tracking systems.
Qualifications, Experience & Skills:
Registered Nurse (RN), Certified Coding Specialist (CCS), Certified Clinical Documentation Specialist (CCDS), or other relevant clinical or coding certification required.
Bachelor’s degree in science, Pharma, Nursing, Health Information Management, or a related field preferred.
Minimum of 5-7 years of experience in clinical documentation improvement, coding, or related healthcare field.
Strong knowledge of medical terminology, anatomy and physiology, and disease processes.
Experience working with electronic health record (EHR) systems.
Excellent communication and interpersonal skills.
Strong analytical and problem-solving abilities.
Ability to work independently and as part of a team.
Excellent organizational and time-management skills.
Proficiency in using Microsoft Office Suite.
Certifications:
Required: RN, CCS, CCDS, or other relevant clinical or coding certification.
Experience with EPIC preferred but not mandatory
Both Hospital and Professional CDI experience preferred
Flexible to work from Office all 5 days in the week
Clinical Documentation Improvement Specialist (CDI)
Posted 3 days ago
Job Viewed
Job Description
Thryve Digital Health LLP is an emerging global healthcare partner that delivers strategic innovation, expertise, and flexibility to its healthcare partners. Being a US healthcare conglomerate captive, we have direct access to deeper insights that help us accelerate our learning process and keeps us ahead of the curve. Thryve delivers next-generation solutions that enable our healthcare partners to provide positive experiences to their consumers.
Our global collaborative of healthcare, operations, and IT experts creates innovative and sustainable processes for our clients, which keeps the ever-evolving consumers engaged and assists them in managing the future of their healthcare better. We recognize that our people are our strength and the diverse talents they bring to our global workforce are directly linked to our success. Thryve is an equal opportunity employer and places a high value on integrity, diversity, and inclusion in the organization. We do not discriminate on the basis of any protected attribute. For more information about the organization, please visit
Job Title: Senior Clinical Documentation Improvement (CDI) Specialist
Department: Revenue Cycle Management/Clinical Documentation Improvement
Reports To: CDI Manager/Director
Location: Chennai/Hyderabad
Summary:
The Senior CDI Specialist is responsible for leading clinical documentation improvement efforts to ensure accurate and complete medical record documentation that supports appropriate coding, reimbursement, and quality reporting. This role requires expertise in clinical documentation requirements, coding guidelines, and regulatory standards. The Senior CDI Specialist performs comprehensive medical record reviews, collaborates with physicians and other healthcare providers, provides education and training, and serves as a resource for the CDI team.
Key Responsibilities:
Medical Record Review:
- Conduct concurrent and retrospective reviews of inpatient and outpatient medical records to identify opportunities for documentation improvement.
- Evaluate the accuracy and completeness of clinical documentation to ensure it reflects the patient's condition, treatment, and outcomes.
- Identify discrepancies, inconsistencies, and missing information in the medical record.
- Analyze documentation to determine the principal diagnosis, comorbidities, and complications.
Physician Collaboration and Education:
- Communicate with physicians and other healthcare providers to clarify documentation and obtain additional information.
- Provide education and training to physicians and other healthcare providers on documentation requirements, coding guidelines, and regulatory standards.
- Conduct one-on-one education sessions with physicians to address specific documentation deficiencies.
- Develop and deliver educational materials, presentations, and workshops on CDI topics.
Coding and Reimbursement:
- Ensure that documentation supports accurate coding and billing practices.
- Collaborate with coding staff to resolve coding discrepancies and documentation issues.
- Understand the impact of documentation on reimbursement and DRG (Diagnosis Related Group) assignment.
- Stay current on changes in coding guidelines (ICD-10, CPT, HCPCS) and reimbursement policies.
Data Analysis and Reporting:
- Collect and analyze data related to CDI activities, including query rates, physician response rates, and documentation improvement metrics.
- Prepare reports and presentations on CDI performance and trends. Identify opportunities to improve CDI processes and outcomes.
- Participate in quality improvement initiatives and performance improvement projects.
Regulatory Compliance:
- Ensure compliance with all applicable regulatory requirements, including HIPAA, CMS (Centers for Medicare & Medicaid Services), and Joint Commission standards.
- Stay current on changes in regulatory requirements and guidelines related to clinical documentation and coding.
- Participate in internal audits and external reviews of clinical documentation.
Team Leadership and Mentorship:
- Serve as a mentor and resource for junior CDI Specialists.
- Provide guidance and support to the CDI team on complex cases and documentation challenges.
- Assist in training new team members on CDI processes and procedures.
- Participate in team meetings and contribute to the development of CDI strategies.
System Proficiency:
- Utilize electronic health record (EHR) systems and CDI software to manage medical record reviews and documentation queries.
- Maintain accurate and up-to-date information in CDI tracking systems.
Qualifications, Experience & Skills:
- Registered Nurse (RN), Certified Coding Specialist (CCS), Certified Clinical Documentation Specialist (CCDS), or other relevant clinical or coding certification required.
- Bachelor’s degree in science, Pharma, Nursing, Health Information Management, or a related field preferred.
- Minimum of 5-7 years of experience in clinical documentation improvement, coding, or related healthcare field.
- Strong knowledge of medical terminology, anatomy and physiology, and disease processes.
- Experience working with electronic health record (EHR) systems.
- Excellent communication and interpersonal skills.
- Strong analytical and problem-solving abilities.
- Ability to work independently and as part of a team.
- Excellent organizational and time-management skills.
- Proficiency in using Microsoft Office Suite.
Certifications:
- Required: RN, CCS, CCDS, or other relevant clinical or coding certification.
- Experience with EPIC preferred but not mandatory
- Both Hospital and Professional CDI experience preferred
- Flexible to work from Office all 5 days in the week
Client Partner - Non-Clinical Documentation Services
Posted today
Job Viewed
Job Description
Process non-clinical transactions with a high degree of accuracy
The process involves viewing documents on the screen, identifying, and capture of the right information on the right fields. The document types include prescriptions, lab reports, and imaging documents.
To be considered for this position, applicants need to meet the following qualification criteria:
Graduates in any non-engineering courses. People who have completed a 3-year diploma course may also apply
Basic typing (20 WPM) and good communication skills
Willingness to work in different shift
Preference will be given to healthcare BPO professionals with experience in non-voice processes, good typing, and interpersonal skills, along with a good overall performance track record
We are also hiring fresh graduates as Assistant Client Partners.
Clinical Data
Posted today
Job Viewed
Job Description
• Utilizes graphs, pivot charts, and other mechanisms as needed.
• Writes SQL queries to efficiently retrieve business data to respond to requests from c-suites, VPs, Directors, and clinical administration.
• Maintain proficiency in data quality management, understanding quality root cause analysis, remediation options analysis, and measuring and communicating team and individual success.
• Ensure integrity of the data pulled from Clinical systems and databases and identifies and resolve issues that arise with these systems.
• Clears EPHR interface data errors daily, including HL7 analysis.
Clinical Data Specialist
Posted 4 days ago
Job Viewed
Job Description
Provide comprehensive data management expertise to eCOA Data Management to provide efficient, quality data management products that meet customer needs. Provide support in operational eCOA Data Management activities to the eCOA Data Team Lead (DTL) or operate in a specific eCOA DM task (e.g., lead of a task on a megatrial, data reconciliation and monitoring).
Essential Functions
- Serve as Data Operations Coordinator (DOC) for several global clinical trials or serve in a leadership role to a specific data management task.
- With minimal guidance, serve as back-up for Data Operations Coordinator or Data Team Lead
- Provide specific eCOA or Clinical DM task or technology expertise. Manage delivery of projects through full data management process life-cycle. With minimal guidance, manage project timelines and quality issues, determine resource needs, and identify and justify out-of-scope. Provide comprehensive data management expertise (including all operations tasks ). Perform comprehensive quality control procedures. Independently bring project solutions to the eCOA DM team.
- communicate ideas for process improvement. Assist in developing and implementing new technology. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with eCOA DM and project teams. Interact with eCOA DM team members to negotiate timelines and responsibilities."
Qualifications
- Working knowledge of SAS software a plus, but not required.
Bachelor's Degree Clinical, biological or mathematical sciences, or related field, or nursing qualification Req
- 3 years of related experience including clinical trials experience in a function similar to data management. Equivalent combination of education, training and experience.
- Thorough knowledge of the data management process. Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology. Previous experience and proven competence in managing delivery of project through full data management study life-cycle (of several large phase I or at least 1 medium size Phase III). Comprehensive understanding of clinical drug development process. Excellent organizational, communication, and data management skills (detail oriented). Ability to establish and maintain effective working relationships with coworkers, managers and clients. Thorough knowledge of the data management process. Knowledge of Medical Terminology, Pharmacology, Anatomy, and/or Physiology. Previous experience and proven competence in managing delivery of project through full data management study life-cycle (of several large phase I or at least 1 medium size Phase III). Comprehensive understanding of clinical drug development process. Excellent organizational, communication, and data management skills (detail oriented). Ability to establish and maintain effective working relationships with coworkers, managers and clients.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
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Clinical Data Specialist
Posted 5 days ago
Job Viewed
Job Description
Role: Clinical Data specialist
Skill: CDM, Rave
Mode: Hybrid
Experience: 2-5 years in Clinical Data management
Job Location: Kochi/Kolkata/Bangalore
Educational Qualification: Any life science graduate
Job Overview:
Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager.
Essential Functions
- Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or serve in a leadership role in a specific data management task (e.g., coder, tester or database designer for technologies that don't require extensive programming expertise) with guidance.
- May serve in the role of back-up to a DOC or DTL.
- May conduct data review.
- May write and resolve data clarifications.
- May lead database audit team.
- May develop and test databases and edit specifications.
- May perform testing of programming.
- May perform clinical data coding. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team."
Qualifications
- Bachelor's Degree Clinical, biological , or related field Req
- Equivalent combination of education, training and experience in lieu of degree.
Clinical Data Specialist
Posted 5 days ago
Job Viewed
Job Description
Role: Clinical Data specialist
Skill: CDM, Rave
Mode: Hybrid
Experience: 2-5 years in Clinical Data management
Job Location: Kochi/Kolkata
Educational Qualification: Any life science graduate
Job Overview:
Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager.
Essential Functions
- Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or serve in a leadership role in a specific data management task (e.g., coder, tester or database designer for technologies that don't require extensive programming expertise) with guidance.
- May serve in the role of back-up to a DOC or DTL.
- May conduct data review.
- May write and resolve data clarifications.
- May lead database audit team.
- May develop and test databases and edit specifications.
- May perform testing of programming.
- May perform clinical data coding. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team."
Qualifications
- Bachelor's Degree Clinical, biological , or related field Req
- Equivalent combination of education, training and experience in lieu of degree.
Clinical Data Manager
Posted 5 days ago
Job Viewed
Job Description
Experience: 5+ yrs
Work Mode: Work from Office
Work Location: Bangalore
LOOKING FOR IMMEDIATE JOINERS ONLY
Job Description - Clinical Data Manager :
OVERVIEW
The Clinical Data Manager (CDM) is an independent role responsible for supporting the study team and developing comprehensive study documentation, designing database specifications, and overseeing validation, maintenance/data cleaning, and closeout activities for clinical trial databases. The CDM is recognized as the platform expert, leveraging cutting-edge tools and technologies to provide continuous data insights and ensure the timely delivery of high-quality results for Sponsors. The CDM has a strong foundation in clinical data management, combined with the agility to adapt as processes evolve towards the integration of clinical data science.
KEY TASKS & RESPONSIBILITIES
• Define project specifications for Data Management services, including Protocol Conversion, Database Build, CRF Design and Data Review and Data Reconciliation tools.
• Understand external data collection, its integration into the clinical trial, and the management and reconciliation processes required to ensure its accuracy and relevance.
• Execute data cleaning strategies to accelerate the time to achieve subject data cleanliness and ensure high-quality, timely deliverables.
• Perform holistic data review and trending analysis via reporting and elluminate® analytics to proactively identify issue, risks and develop mitigation strategies.
• Utilize artificial intelligence (AI) and machine learning (ML) for anomaly and outlier detection to enhance the efficiency and quality of trial data.
• Monitor and interpret key performance indicators (KPIs), metrics, dashboards, Clinical Trial Operational Analytics (CTOA), and reports to provide actionable recommendations to study lead(s)/project manager.
• Perform Query Management
• Define specifications and collaborate with technical team on configuration of centralized data management platform, elluminate® Data Central for data cleaning strategy and oversight activities.
• Prepare and maintain data management documentation (e.g., DMP, CCGs, Help Text, DVS) and update throughout trial lifecycle.
• Review and ensure the quality control of team-developed deliverables, covering eCRFs, study documents, program/report specifications, outputs, and elluminate® Data Central with analytics modules. Actively evaluate and contribute to enhance processes to increase efficiency and effectiveness.
• Collaborate and work as a team to ensure the deliverables are completed on time with high quality.
• Ensure compliance with industry quality standards, regulations, guidelines, and procedures.
• Other duties as assigned.
CANDIDATE’S PROFILE:
Education & Experience
• 5+ years’ experience in Clinical Data Management preferred.
• Bachelor’s degree in a health-related field or equivalent experience preferred.
• CCDM Certification preferred.
Professional Skills
• Strong project management experience and project team leadership skills including work planning, work delegation and solving complex problems.
• Strong analytical and strategic thinking skills
• Detail oriented, ability to multitask with strong prioritization, planning and organization skills.
• Excellent collaborative skills
• Demonstrated command of the English language with proficiency in both verbal and written communication
Technical Skills
• Proficiency in Microsoft Office Applications, specifically MS Project and MS Excel
• Knowledge of ICH/GCP guidelines, 21 CFR Part 11 and clinical trial methodology
• Proficient with EDC and Clinical Data Management Systems
• Experience with Cloud SaaS platforms (preferred)Experience with data reporting tools such as Qlik, JReview, Spotfire preferred.
• Experience with RBQM methodology preferred.
• Exposure to CDISC guidelines and standards