Clinical Documentation Jobs in India

Job Title: Physiotherapist Germany (B2 German Required)Location: GermanyIndustry: Healthcare / Medical / RehabilitationEmployment Type: Full-TimeExperience Required: Minimum 3 YearsLanguage Requirement: German B2 or Higher (Mandatory)Job Summary:We are seeking a skilled and compassionate Physiother...

Responsible for overseeing quality systems and regulatory compliance across clinical trials involving biological products. This role ensures that all clinical research activities meet global regulatory standards internal policies and Good Clinical Practice (GCP) guidelines. The Lead will collaborate...

Job Title: Physiotherapist Germany (B2 German Required)Location: GermanyIndustry: Healthcare / Medical / RehabilitationEmployment Type: Full-TimeExperience Required: Minimum 3 YearsLanguage Requirement: German B2 or Higher (Mandatory)Job Summary:We are seeking a skilled and compassionate Physiother...

At EY were all in to shape your future with confidence.Well help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go.Join EY and help to build a better working world.Discipline Design for TechnologyRole Type Visual DesignThe opportunityEY G...

Job descriptionAsaClinicalDocumentSpecialistIyouwillberesponsibleforreviewingessential/.DoyouthinkyouhavewhatittakestobeaClinicalDocumentSpecialistIChecktheroledescriptionbelow:Job requirementsResponsibilities:Review documents in eTMF workflow to complete initial Indexing.Maintain defined quality st...

Job Family:Coding OP (India)Travel Required:NoneClearance Required:NoneWhat You Will Do:-1. *Team Management*: Supervises and guides a team of medical coders providing guidance training and support to ensure high-quality coding output.2. *Process Improvement*: Identifies areas for process improvemen...

JOB DESCRIPTION:Scientific /Medical Writer:Role OverviewThe Medical Writer is an essential individual contributor within the Clinical Science Teamresponsible for independently authoring high-quality clinical documentsparticularly Module2.5 (Clinical Overview) and Module 2.7 (Clinical Summary)for g...

Create impactful technical documentation for global engineeringDo you want to be part of a global team contributing to the green transition through innovative cable solutions At NKT we are looking for a meticulous and creative Document Specialist to join our Applied Engineering team in this role yo...

JOB DESCRIPTIONJob Title: CTA-ClinOpsJob Location: Bangalore Department: CLINICAL OPERATIONS T&CRAbout Syngene: Syngene () is an innovation-led contract research development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene...

Responsible for HSC coding operations and clinical documentation improvement operations (as applicable) ensuring timeliness accuracy completeness consistency compliance and standards fulfillment as defined in HSC Service Level Agreements (SLAs) Contributes to the development of strategic dir...

Medical Coder Job Offer We are seeking a detail-oriented and experienced Medical Coder to join our esteemed healthcare organization in Coimbatore Tamil Nadu. This full-time position offers a fantastic opportunity for professionals with 2 to 8 years of experience in medical coding and a strong unders...

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process expeditable advers...

Job Overview:Line manage PSS staff including performance reviews human resource issues and assists Senior PSS Management in assigning resources to projects. The post holder is typically but not exclusively responsible for providing line management of junior PSS staff. Manage coordinate and oversee t...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionAt Thermo Fisher Scientific you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner a...

Job Overview:Assist with the overall Clinical Safety and/or PSS operations associated with products including the entire adverse events process which may include safety data collected from clinical trials and/or post marketing setting (i.e. unsolicited reports). Manage and process expeditable advers...

Job Title: Medical Record Audit SpecialistJob Summary:We are seeking a detail-oriented and experienced Medical Record Audit Specialist to review analyze and ensure the accuracy and compliance of medical records. The candidate will be responsible for auditing patient records to maintain quality stand...

Summary of Responsibilities:Performs supervisory duties for Document Specialists (DSs) including but not limited to interviewing hiring training developing performance evaluation intervention discipline and discharge.Organizing gathering scanning and filing of all applicable documents into appropria...

Job Overview:Responsible for general maintenance and any required archival of documents produced by the CPS Project Management Team. Organizing gathering scanning and filing of all applicable documents into appropriate electronic and/or paper copy locations including the Trial Master File (TMF) as d...

At EY were all in to shape your future with confidence.Well help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go.Join EY and help to build a better working world.Job Title: Healthcare ConsultantDomain: Global Healthcare -Experience Requ...

Job DescriptionUnder the oversight of the line-manager this role is responsible for comprehensive trial and site administration and involves preparing collating distributing and archiving clinical documents. The CTC supports clinical supply & non-clinical supply management and ensures timely mainten...