Clinical Data Associate III

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profile Job Location:

Mexico City - Mexico

profile Monthly Salary: Not Disclosed
Posted on: Yesterday
Vacancies: 1 Vacancy

Job Summary

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

At Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life To enable our customers to make the world healthier cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research development and delivery of life-changing therapies. As part of our clinical research portfolio our CorEvitas evidence-based solutions specialize in generating data intelligence and clinical insights needed to bring safe and effective treatments to market. Your objectivity and dedication to patient safety will improve health outcomes that people and communities depend on now and in the future.

Location/Division Specific Information w

#CorEvitas

Discover Impactful Work:

As part of the Clinical Data Management (CDM) team the Coder of Clinical Data Management is responsible for coding medical terminology and reviewing coding listings in accordancewith the Coding Plan and/or other related documentation. Identifying data issues and working with the team and sites to resolution. Ensuring coding accuracy according to departmental procedures as well as ensuring all coding aspects are conducted accurately and deliverables are completed to quality expectations and on time.

A day in the Life:

The Coder must be able to efficiently organize the workload and code medical terminology in accordance with Good Clinical Practice (GCP) Standard Operating Procedures (SOPs)/Work Instructions (WIs) and other related documentation.

ESSENTIAL FUNCTIONS

  • Assists in providing general and project specific coding training to CDM staff perform coding activities.
  • Provides support guidance and direction on all coding aspects to the registry team.
  • Produces registry-specific status reports on a regular basis.
  • Acts as a mentor providing ongoing advice and guidance to Coding Specialists.
  • Collaborate with Director CDM on Coding-specific processes.
  • Perform other duties as required by the Department.

Keys to Success:

Education

  • Bachelors degree or equivalent and relevant formal academic / vocational qualification / experience such as an Associates degree in combination with relevant coding certifications / experience.

Experience

  • 4 or more years experience in relevant Clinical Coder role.

Knowledge Skills Abilities

  • Should have strong experience in WHODD and MedDRA dictionaries
  • Should have strong working experience in an EDC (i.e. Zelta Medidata Rave Veeva)
  • Applies knowledge and skills in a highly organized manner while adhering to regulatory guidelines SOPs and department expectations.
  • Excellent understanding of clinical/medical terminology.
  • Strong attention to detail and skill with numbers.
  • Ability to use interactive computer programs.
  • Good organization skills and analytical/problem solving skills.
  • Ability to work productively with minimal supervision.
  • Ability to maintain a high degree of confidentiality with medical records and 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.
  • Ability to work in a team environment and independently as needed.
  • Demonstrated good judgment in making decisions.
  • Ability to set and meet timelines and/or be able to negotiate schedule changes in response to project demands.
  • Strong English communication and writing skills.

Our Mission is to enable our customers to make the world healthier cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100000 colleagues we share a common set of values - Integrity Intensity Innovation and Involvement - working together to accelerate research solve complex scientific challenges drive technological innovation and support patients in need. #StartYourStory with Thermo Fisher Scientific where diverse experiences backgrounds and perspectives are valued.

Apply today!

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other legally protected status.

Accessibility/Disability Access

Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example this may include individuals requiring assistance because of hearing vision mobility or cognitive impairments. If you are a job seeker with a disability or assisting a person with a disability and require accessibility assistance or an accommodation to apply for one of our jobs please submit a request by telephone at 1-*. Please include your contact information and specific details about your required accommodation to support you during the job application process.

*This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes such as not being able to get into the career website following up on an application or other non-disability related technical issues will not receive a response.


Required Experience:

IC

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

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