Skip to main content
Post your CV and find your next job on Indeed!

Clinical Trials jobs in Scotland

Sort by: -
    • Maintain and prepare for final archival of data management documentation relevant to the assigned clinical trials and assist the corporate archivist in…
    • Helps ensure all study documentation and source data is captured accurately in eCRF, up to date and first time right.
    • Escalates to management as needed.
    • View all Thermo Fisher Scientific jobs - Glasgow jobs - Compliance Officer jobs in Glasgow
    • Salary Search: Corporate Compliance Associate II - Fixed Term Contract salaries in Glasgow
    • See popular questions & answers about Thermo Fisher Scientific
    • Prior sales/clinical support experience preferred.
    • The CS will work with the field in developing research accounts and conduct and follow-up on clinical…
    • 1+ years clinical trial safety experience.
    • Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development…
    • Coordinate clinical supply projects from award through completion, tracking timelines and ensuring on-time delivery.
    • Plus, participate in charitable activities.
    • Cross-Functional Collaboration: Partner closely with internal Clinical Specialists who handle clinical adoption and trials to ensure a seamless, premium…
    • This will require in-depth knowledge of clinical markets and a clear understanding of what clinical customers expect.
  • View similar jobs with this employer
    • Entering clinical trial sites into Marken’s internal database (where necessary).
    • To coordinate and manage shipment bookings and transportation activities,…
  • View similar jobs with this employer
    • Marken offers a state-of-the-art GMP-compliant depot network and logistic hubs for clinical drug product storage and distribution worldwide, and supports cell…
    • Knowledge and understanding of clinical study protocols and schedule of assessments.
    • 2 or more years of experience in clinical research site contracting and…
    • Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical,…
    • Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical,…
    • Relevant experience in clinical selling.
    • Spending time in the OR working alongside our clinical stakeholders providing customer education on the safe and…
    • Lead product evaluations, trials, and conversion projects.
    • Proven success in sales, market development, or clinical training.
    • (Preferred) Post-graduate research experience in a scientific, clinical, or social sciences discipline.
    • (e.g., development of workflows or policy updates;…

People also searched:

clinical audit
clinical data
clinical research
clinical trial

Job Post Details

Clinical Data Manager
Everest Clinical Research
·
4.3
United Kingdom
•
Remote
Permanent
Apply now

Job details

Pay information not provided
Work from home
Permanent
Remote in United Kingdom

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 Corporate headquarters are located in Ontario, Canada and US headquarters in New Jersey, USA, with additional physical offices in Asia and 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.

#LI-Remote
#LI-KD1

Let Employers Find YouUpload Your Resume