Research Insiders

Senior Clinical Coding Specialist

CaidyaIndia - (home based)hybridSalary not postedView the original posting at Caidya ↗

Job Description: Job Title: Senior Clinical Coding Specialist Job Location: India (Remote) Job Overview: Perform medical coding of free texts collected in the course of a clinical trial or from other sources, taking into account, appropriate coding guidelines and to act as Subject Matter Expert on all clinical coding matters including dictionary licensing, impact of new dictionary releases, and the use of clinical coding software applications. Job Duties and Responsibilities: The specific job duties of a Senior Clinical Coding Specialist may include duties of Clinical Coding Specialist I and II and not limited to the following: Responsible for providing technical, procedural, and subject matter leadership across multiple projects assigned to the Clinical Coding team ensuring that team members deliver in accordance with SOPs, best practices, and agreed timelines. Assign codes to unambiguous reported terms according to agreed coding guidelines for a given project Generate coding related queries and Query management in Databases Communicate issues that require sponsor decision, including proposal for a solution Ensure consistent code assignment within a project by reviewing coding and re-assignment of terms, if necessary. Perform up-versioning of medical coding dictionaries and clinical trial data. Provide independent review of data coded by third parties, if needed. Responsible for completeness, timely delivery, and quality of clinical data Provide support to other departments concerning dictionary use and code assignment Create and review Coding Guidelines/conventions including SOP revision as needed. Provide input to protocol writing, Data Management Plan, database setup and CRF design process with respect to coding. Performing Test data creation & User Acceptance Testing, Provide Coding Metrics, Coding status reports with Lead Data Manager/Sponsor as per requirement. Maintaining Clinical Study Documents and archiving as appropriate. Responsible for completeness, timely delivery, and quality of clinical data. Continuous improvement of departmental processes and procedures to ensure DM is consistently maximizing efficiencies, leveraging technology, and incorporating innovation to optimize delivery Maintains working knowledge of regulatory requirements/guidance as well as industry leading best practices to ensure the company’s DM procedures are in line with industry expectations Assist in training new staff. Attend and participate in project/company meetings including occasional off hour calls to coincide with offices in other time zones Handling customer requests and developing customer relationship and communication Other duties as assigned Supervisory Responsibilities: No supervisory responsibilities. Job Requirements: Education Bachelor’s degree or equivalent in pharmacy, nursing, or science field preferred Experience Minimum of 7 years’ professional experience in the pharmaceutical industry, clinical research or at a CRO Clinical Research industry experience in Data Management or Clinical Coding required. Skills/Competencies Extensive experience in clinical coding of medical verbatim terms collected in clinical studies across different therapeutic areas. Expert knowledge of MedDRA, WHODrug Global dictionaries and clinical coding best practices. Proficiency in medical terminology as well as body systems/anatomy, physiology, and concepts of disease Comprehensive knowledge of GCP/ICH guidelines Able to exercise judgment within defined procedures and practices and to determine appropriate action independently Good overview of all systems linked to the coding process, and understanding of their interactions and dependencies Good understanding of Clinical Data Management process Extensive experience in using Clinical Coding software applications in combination with EDC systems. Good level of English (verbal and written) Strong problem-solving abilities (technical, interpersonal, and decision making) Capabilities Strong computer s

The people who work here are one introduction away.

We show you who they are and write your first message — the insider list for this posting is filling in now. You have one introduction. The rest follows.

People at Caidya you can reach out to

36 of 55 public LinkedIn profiles found in searches for Caidya list Caidya in their headline — those are the ones you can be confident work there. Pick who to reach out to — we'll draft your message; you make the contact. The rest, when shown, are marked Unverified.

Profiles are public pages as indexed by the search engine — we never log in to LinkedIn or copy private data, and anyone can ask to be removed. Ask to be removed →

Related Clinical data jobs, hiring now