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Senior Clinical Data Manager

Employer
Worldwide Clinical Trials
Location
Nottingham, GB
Salary
Competitive
Start date
21 Nov 2020
Closing date
21 Dec 2020

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Job Details

Worldwide Clinical Trials is hiring a Senior Clinical Data Manager to join our growing team!

The Senior Clinical Data Manager will provide leadership, management and technical expertise within the assigned projects to ensure that they are executed in an efficient, accurate and timely manner to the Sponsor's satisfaction.

RESPONSIBILITIES:
Tasks may include but are not limited to:
  • To manage each of the data management projects to which assigned; provide leadership to the corresponding data management teams.
  • To represent WCT in all dealings with Sponsors with respect to the Data Management aspects of the projects to which assigned.
  • To liaise with the Director, Data Management at regular intervals to discuss progress and any issues outstanding.
  • To take responsibility for staff training for all projects to which assigned; both direct involvement in training and supervision of staff assigned to training.
  • To liaise and collaborate with corresponding teams in other WCT departments working on the same project.
  • To ensure that all data management operations are conducted to WCT SOPs; contribute to the ongoing revision/improvement of these SOPs.
  • To create and review project specific documentation for assigned trials, i.e. the Data Management Plan and the Data Management File.
  • To write specifications for the set-up and modification of database and edit check specifications for assigned projects.
  • To write and validate Manual and SAS checks.
  • To set-up processes for reconciliation and perform reconciliation of data from external sources (e.g. Serious Adverse Events, IVRS, Central Laboratory).
  • To perform verification and User Acceptance Testing of configured databases.
  • To support and oversee all data cleaning activities for assigned projects.
  • To specify and review SAS listings/SAS tables for assigned projects.
  • To create and review CRF and eCRF completion guidelines, EDC system manuals and access instructions.
  • To train others to make full and correct use of the company Data Capture systems, when used, for the collection of clinical data.
  • To produce information/reports directly from the clinical database or via the appropriate procedure to request a new report from the appropriate department or vendor.
  • To liaise with personnel at the sponsor company, or their designates, with Central Event Adjudication Committees (CEC) within clearly defined guidelines for matters concerning processing of data.
  • To ensure that adequate QC checks (including spot checks) and Database Quality Assessments on the clinical databases of assigned projects.
  • To ensure timely database locks for all assigned projects.
  • To participate as necessary in sponsor audits, regulatory authority inspections and other third party meetings. Ensure that any recommendations are discussed and that solutions are incorporated.

OTHER SKILLS AND ABILITIES:
  • The job holder must be computer literate and numerate with a willingness to adapt to various computer systems.
  • It is essential that the job holder works with close attention to detail and is questioning about the validity of the data being entered and has an ability to phrase data queries in an understandable and impartial manner.
  • To have the ability to train new staff and to monitor their performance.
  • Proven project delivery skills.
  • Several years experience within Data Management or associated field.

REQUIREMENTS:
  • Educated to degree level (preferably Life Science), Nursing qualification, or relevant industry experience Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.

#LI-HD1

Company

Find out more about working for our company

Worldwide Clinical Trials -hub-button

Brief Company Description; 

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,000 experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

 

Company info
Website
Mini-site
Worldwide Clinical Trials
Telephone
+44 115 956 7711
Location
1st Floor Waterfront House
Beeston Business Park
Beeston
Nottingham
Nottinghamshire
NG9 1LA
United Kingdom

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