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Coding Specialist (Smolensk, Russia)

Pharmaceutical Product Development (PPD)

RU-Smolensk-Smolensk RU 65 B Shevchenko S

We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health.You will be joining a trulycollaborative and winning culture as we strive to bend the time and cost curve of deliveringlife-saving therapies to patients.

Are you a data and a people person? Here’s your team. We manage and clean the data collected in a clinical trial — from the design and build of the database and edit checks, through the entry and cleaning of data to the final delivery of clinical trial data. We work closely with the project teams and clients to identify best practices and processes, meet and exceed our clients’ needs, and do the right thing to earn their trust.

Coding Specialist

You will participate in the creation of study specific coding conventions and perform coding of medical terminology. Your responsibilities will include review of coding, raising coding queries and updating the clinical database as required. You will also provide support to other members of the coding group. The objective of a Coding Specialist is to code medical terminology in accordance with Good Clinical Practices (GCP), Standard Operating Procedures (SOPs)/Working Practice Documents (WPDs) and Data Validation Manuals (DVMs).

Codes medical terminology and reviews coding listings in accordance with the Coding Plan in the DVM Identifies data issues and works with PPD team and study sites to resolve Ensures coding accuracy according to departmental operating procedures Ensures all coding aspects are conducted accurately, and all coding deliverables are completed to quality expectations, within budget and on time

We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health.You will be joining a trulycollaborative and winning culture as we strive to bend the time and cost curve of deliveringlife-saving therapies to patients.

Are you a data and a people person? Here’s your team. We manage and clean the data collected in a clinical trial — from the design and build of the database and edit checks, through the entry and cleaning of data to the final delivery of clinical trial data. We work closely with the project teams and clients to identify best practices and processes, meet and exceed our clients’ needs, and do the right thing to earn their trust.

Coding Specialist

You will participate in the creation of study specific coding conventions and perform coding of medical terminology. Your responsibilities will include review of coding, raising coding queries and updating the clinical database as required. You will also provide support to other members of the coding group. The objective of a Coding Specialist is to code medical terminology in accordance with Good Clinical Practices (GCP), Standard Operating Procedures (SOPs)/Working Practice Documents (WPDs) and Data Validation Manuals (DVMs).

Codes medical terminology and reviews coding listings in accordance with the Coding Plan in the DVM Identifies data issues and works with PPD team and study sites to resolve Ensures coding accuracy according to departmental operating procedures Ensures all coding aspects are conducted accurately, and all coding deliverables are completed to quality expectations, within budget and on time

Education and Experience

· Bachelor's degree OR certification in a related allied health profession from an appropriately accredited institution

· At least 1 year experience in a data management environment

Knowledge, Skills and Abilities:

Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, SOPs and client expectations Excellent understanding of clinical/medical terminology Strong attention to detail and skill with numbers Ability to use interactive computer programs Good written and verbal communication skills Good organizational skills Good analytical/problem-solving skills Ability to work productively with minimal supervision Ability to maintain a high degree of confidentiality with medical records and client's proprietary data Ability to attain, maintain and apply a working knowledge of GCPs and applicable SOPs Strong customer focus and excellent interpersonal skills Proven flexibility and adaptability

Education and Experience

· Bachelor's degree OR certification in a related allied health profession from an appropriately accredited institution

· At least 1 year experience in a data management environment

Knowledge, Skills and Abilities:

Ability to effectively apply knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, SOPs and client expectations Excellent understanding of clinical/medical terminology Strong attention to detail and skill with numbers Ability to use interactive computer programs Good written and verbal communication skills Good organizational skills Good analytical/problem-solving skills Ability to work productively with minimal supervision Ability to maintain a high degree of confidentiality with medical records and client's proprietary data Ability to attain, maintain and apply a working knowledge of GCPs and applicable SOPs Strong customer focus and excellent interpersonal skills Proven flexibility and adaptability

Job posted: 2020-10-21

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