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    • Assist in resolving data coding discrepancies resulting from the coding of medical events, treatment procedures, and medications.
    • Experience of healthcare interoperability standards (HL7, FHIR) and the wider clinical data landscape.
    • Build and maintain integrations against healthcare…
    • Our work is varied and always evolving – from supporting high profile financial and performance turnaround projects to developing long term demand and capacity…
    • Our work is varied and always evolving – from supporting high profile financial and performance turnaround projects to developing long term demand and capacity…
    • The Lead Clinical Data Manager (LCDM) is accountable for clinical data management activities in support of the clinical pipeline for complex studies.
    • Provide guidance with adverse event (MedDRA) and drug (WHODrug) coding for clinical and post-marketing safety data.
    • Knowledge of drug development process.
    • Ideally have a working knowledge of clinical systems such as SystmOne or EMISweb.
    • Current registration with GMC and NHS performers list and engaged in regular…
    • Provide guidance with adverse event (MedDRA) and drug (WHO Drug) coding for clinical and postmarketing safety data.
    • Dealing with non clinical admin triage requests.
    • Daily filing, coding and task delegation associated with our administrative email account.
    • Oversee medical and safety aspects of studies, including Site Initiation Visits, ongoing safety reviews, medical coding, and safety reporting.
    • Work directly with product, design, and clinical teams.
    • The product combines regular blood tests, longitudinal health data, behaviour-change science and AI…
    • Fluency with AI coding tools: You use modern AI tools to accelerate delivery, while staying rigorous about correctness and validation.
    • Oversee overall quality of the clinical database.
    • Experience in utilizing various clinical database management systems.
    • Experience using SNOMED CT, ICD-10 or related clinical coding systems.
    • Contributing to exploratory phenotype mapping work using clinical coding systems such as…
    • Oversee overall quality of the clinical database.
    • Experience in utilizing various clinical database management systems.

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Job Post Details

Clinical Data Manager - job post

Everest Clinical Research
4.2 out of 5 stars
United Kingdom•Remote
Permanent

Job details

Job type

  • Permanent

Benefits

Pulled from the full job description

  • Work from home

Full job description

Everest Clinical Research (“Everest”) is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.

Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest’s headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater New York City Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan.

Everest also recently completed the acquisition of August Research. August Research is a European CRO that provides Clinical Operations and Pharmacovigilance services to a wide variety of pharmaceutical and biotechnology clients. The Company has worked on over 120 projects for Phase I-IV clinical trials across multiple therapeutic areas including cardiovascular, infectious disease, oncology and rare disease. The acquisition of August Research establishes a European footprint for Everest to provide full-service offerings to its pharmaceutical, biotechnology and medical devices clients, and other operational capabilities through the Company’s substantive experience and infrastructure across 14 countries in Western and Eastern Europe.

Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients’ needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.

Quality is our backbone, customer-focus is our tradition, flexibility is our strength…that’s us…that’s Everest.

To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Clinical Data Manager remotely from a home-based office anywhere in the the UK in accordance with our Work from Home policy.

Key Accountabilities:

  • Plan, manage, control, and perform data processing and management activities for assigned projects. These tasks are performed in a timely and accurate manner and in compliance with trial Sponsors’ requirements.
  • Lead assigned data processing and management projects by applying project management skills, data processing, and management techniques. Manage timelines and coordinate activities for assigned projects.
  • Specify database validation checks for assigned studies. Lead efforts in developing and maintaining standard database validation checks for common modules as well as for therapeutic/drug area specific modules.
  • Define and monitor clinical trial dataflow and quality control (QC) processes in accordance to corporate Standard Operating Procedures (SOPs), Good Working Practices, and unit guidelines. Perform clinical trial site monitors’ training on dataflow and QC processes.
  • Design and review patient Case Report Forms (CRFs) and database schema. Test data capture/entry screens.
  • Accurately and efficiently validate electronically captured data. Write clear queries on missing data and data points failing pre-defined range checks and/or logical checks. Lead efforts in building a standard query library for common database modules, as well as for therapeutic/drug area specific modules.
  • Perform QC procedures on assigned database during the trial and additional database closure checks at the end of the study.
  • Train and supervise Data Entry personnel and junior data management personnel on study procedures, study specific handling, and management of trial data.
  • Validate and distribute study progress status reports to internal and external study team members.
  • Assist in resolving data coding discrepancies resulting from the coding of medical events, treatment procedures, and medications.
  • Maintain and prepare for final archival of data management documentation relevant to the assigned clinical trials and assist the corporate archivist in assembling and archiving clinical trial data and study documentation.
  • Cooperate with and assist, when required, data management quality assurance (QA) personnel in performing QA procedures on trial CRFs, database schema, and databases for assigned studies.

Qualifications and Experience:

  • A Bachelors’ degree in health and/or pharmaceutical sciences, physical/biological, or chemistry fields with at least 2 years experience in clinical trial data capture and management, or a Master’s or Ph.D degree in these fields with at least 1 year relevant experience.
  • In-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical data management, as well as pharmaceutical clinical trial regulations, industry guidance, conventions and standards.
  • Strong leadership in clinical data management activities and a desire to excel in leading data management projects.

To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.ecrscorp.com (http://www.ecrscorp.com)

We thank all interested applicants, however, only those selected for an interview will be contacted.

Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.

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