logo

+44 208 985 0565

Clinical Data Manager interim


This job does not exist anymore.

Try running a new search or browse our vacancies.

Or fill in the form below to receive job alerts.

https://www.pop-science.co.uk/1151-clinical-data-manager-interim/clinical-research/central-london/job2020-08-23 09:44:151970-01-01 Pop Science
Job Type Permanent Full Time
Location London
Area Central London, UK Central London UK London
Sector Clinical Research
Salary Based on experience
Currency gbp
Start Date ASAP
Advertiser remoteapi
Job Ref 938
Job Views 612
Description

We've got an interim clinical data manager role for a good, technical data manager. The role is home based due to COVID and will be for 3 months. 

The Data Manager (Interim) role will be responsible for executing standard data management tasks in clinical research studies, including performing data checks and reconciliations, preparation of departmental and project documentation, and execution of interim and final data transfers.

The Company is an innovative company, who are growing rapidly. You will need to be able to learn their data management systems quickly, especially exporting and integrating data. It's an interesting role for someone able to work with agility across multiple projects employing good communication skills, to work with different teams from across and outside the company, including external clients, as you need to deliver to strict deadlines.

Responsibilities:

  • Perform routine and ad hoc hygiene checks on project data.
  • Perform Data Reconciliation of external data.
  • Configure database extracts to support data transfers.
  • Validate the transfer/data prior to submission to sponsor.
  • Writing standard Data Transfer Agreement and Image Transfer Agreements.
  • Perform standard Data and Image Transfers.
  • Perform QC on aspects of work performed in Data Management to ensure that data quality and integrity is maintained.
  • Interact with other project team members to support the set-up, maintenance, and closure of the Data Management aspects of projects.
  • Working knowledge of each of the tasks performed within the department, and to be able to provide coverage for a broad range of tasks as and when required.

Requirements:

  • Bachelor's degree or equivalent data management experience.
  • Strong experience of working in data management within a clinical trials environment essential, ideally with a good understanding of data integration of lab or image data
  • Strong IT skills essential (working within cloud-based database systems desirable) and demonstrate experience of working with a variety of data formats
  • Strong attention to detail.
  • Excellent communication and interpersonal skills.
  • Team oriented and flexible; ability to function in high volume environment with competing priorities.
  • Ability to perform multiple tasks simultaneously under direction and prioritise workload.
  • Working knowledge of Microsoft Office (in particular Excel).
  • Ability to learn other computer systems, including databases.
  • Experience in using SAS platform desirable but not essential.

#medicalimaging #clinicaldatamanagement #clinicalresearch #clinicalresearchers #clinicaldata #clinicalmanagement

Keywords
SectorClear
AreaClear
Job TypeClear
SalaryClear
CurrencyClear
Sign in
Register
Similar Jobs
  • CMC Regulatory Affairs Consultant
    UK, Central London
    Clinical Research
    £0 per year

    Position Summary

    We are seeking an experienced freelance CMC Regulatory Affairs Consultant to support the development, submission, and lifecycle management of regulatory CMC documentation for biologics, pharmaceuticals and/or advanced therapies. The consultant will provide strategic and ope...

  • Non-Clinical Expert/Signatory
    UK, Central London
    Clinical Research
    £0 per year

    Freelance Non-Clinical Expert (EU/UK-Based)

     

    We are seeking an experienced freelance Non-Clinical Expert to act as a regulatory signatory for non-clinical overviews in the EU/UK. The ideal candidate will be capable of reviewing and signing non-clinical reports and non-clinical s...

  • Senior Medical Device Consultant (with SaMD)
    UK, Central London
    Clinical Research
    £0 per year

    We are seeking a freelance Senior Medical Device Consultant with experience in class I-III medical devices and software as a medical device (SaMD). The successful candidate should have a thorough knowledge and understanding of the Software Life Cycle processes, be able to conduct thorough technic...

Email Me Jobs Like This
Subscribed to similar jobs notifications
We use cookies to provide you with the best possible browsing experience on our website. You can find out more below.
Cookies are small text files that can be used by websites to make a user's experience more efficient. The law states that we can store cookies on your device if they are strictly necessary for the operation of this site. For all other types of cookies we need your permission. This site uses different types of cookies. Some cookies are placed by third party services that appear on our pages.
+Necessary
Necessary cookies help make a website usable by enabling basic functions like page navigation and access to secure areas of the website. The website cannot function properly without these cookies.
ResolutionUsed to ensure the correct version of the site is displayed to your device.
essential
SessionUsed to track your user session on our website.
essential
+Statistics
Statistic cookies help website owners to understand how visitors interact with websites by collecting and reporting information anonymously.
Google AnalyticsGoogle Analytics is an analytics tool to measure website, app, digital and offline data to gain user insights.
Yes
No
Money Penny
Yes
No

More Details