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Coding Specialist

4-6 Years
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Job Description

Job Description :

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Join Us as a Coding Specialist - Make an Impact at the Forefront of Innovation
The Coding Specialist codes medical terminology in accordance with Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs)/Working Practice Documents (WPDs) and Data Validation Manuals (DVMs).

What You'll Do:
. Code medical terminology and review coding listings in accordance with the Coding Plan in the DVM.
. Identify data issues and work with Thermo Fisher team and study sites to resolve.
. Ensure coding accuracy according to departmental operating procedures.
. Ensure all coding aspects are conducted accurately, and all coding deliverables are completed to quality expectations, within budget and on time.
. Provide support, guidance and direction on all coding aspects to the CDM project team.
. Produce project-specific status reports for supervisor and for clients on a regular basis.

Education & Experience Requirements:
. High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification
. Technical positions may require a certificate
. Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to at least 4 years).

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills, Abilities:
. Applies knowledge and skills in a highly organized fashion while adhering to regulatory guidelines, global SOPs and client expectations
. Excellent understanding of clinical/medical terminology with strong attention to detail
. Ability to use interactive computer programs.
. Good written and verbal communication skills and a strong command of English language and grammar
. Good organizational and 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
. Strong customer focus and excellent interpersonal skills.
. Proven flexibility and adaptability, able to work in a team environment and independently as needed
. Must demonstrate good judgment in making decisions
. Understands project protocol and Data Validation Manual

Working Conditions and Environment:
. Work is performed in an office environment with exposure to electrical office equipment.
. Frequently drives to site locations and frequently travels both domestic and international.

Why Join Us

When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You'll work in an environment where collaboration and development are part of the everyday experience-and where your contributions truly make a difference.

Apply today to help us deliver tomorrow's breakthroughs.



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About Company

Thermo Fisher Scientific Inc. is an American supplier of scientific instrumentation, reagents and consumables, and software services. Based in Waltham, Massachusetts, Thermo Fisher was formed through the merger of Thermo Electron and Fisher Scientific in 2006. Thermo Fisher Scientific has acquired other reagent, consumable, instrumentation, and service providers, including: Life Technologies Corporation (2013), Alfa Aesar (2015),Affymetrix (2016),FEI Company (2016), BD Advanced Bioprocessing (2018),and PPD (2021).
As of 2017, the company had a market capitalization of $21 billion and was a Fortune 500 company. Annual revenue in 2021 was US$39.21 billion.
In March 2020, Thermo Fisher Scientific received emergency use authorization from the FDA for a test for SARS-CoV-2 to help mitigate the COVID-19 pandemic.

Job ID: 145380425

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