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Clinical Data Manager, Lead

Covance 3/13/2018 2:54:47 PM
JOB ID: 18175 Category: Other
Princeton, New Jersey

   

 

Job Overview

Data management leadership on a large I global project, or multiple projects with responsibility for the development of the project Data Management Plan; data management systems set-up; and data accession, data entry and data review specifications and processes; and oversight of data management activities for the delivery of clinical data according to client quality and integrity specifications, and project timelines and budgets.

+ Develop and maintain a close liaison with project client contacts, core team members, and Project Managers to drive the data management aspects of project delivery.

Education/Qualifications

* University/college degree (life science, pharmacy or related subject preferred), or certification
* in a related al lied health profession from an appropriately accredited institution (e.g., nursing ce11ification, medical or laboratory technology).
* Additional relevant work Experience will be considered in lieu of formal qualifications.
* Broad knowledge of drug development processes.
* Understanding of global clinical development budgets and relationship to productivity targets.
* Knowledge of effective clinical data management practices.
* Knowledge oftime and cost estimate development and pricing strategies.
* Thorough knowledge of TCH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs, especially as related to data handling and processing.

Experience

Minimum five (5) years relevant work Experience in data management with approximately one (1) year technical supervisory Experience to include data management, clinical operations, and knowledge of several therapeutic areas.

* Demonstrated skill for technical management of staff exceeding 5 employees.
* Financial management of gross revenues in excess of $250K per
* Excellent oral and written communication and presentation skills.
* In depth knowledge of clinical trial process and data management, clinical operations, biometrics, quality management, and systems applications to support operation
* Working knowledge of the relationshi p and regulatory obligation of the CRO industry with pharmaceutical I biotechnological-
Ability to lead by example teams on project strategies and achievement of depa11ment goals, objectives, and initiatives and to encourage team members to seek solutions.

* Demonstrated managerial and interpersonal skills


Position Type: Full-Time

Location: Princeton, NJ - New Jersey



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Below is a general Overview of Our Recruiting Process

If you’d like to work for us, please submit your resume/CV online. If your ability to use or access our electronic application is limited due to a disability, please visit www.gettinghired.com or call 1-800-978-4473 for help.

We consider applications from everyone who is interested in a position with us and who meets the required criteria and qualifications.

If your application is selected, someone from our recruiting team will contact you to arrange an initial screen. We may carry this out over the phone or at a face-to-face meeting. You must complete the screen to be considered for the position.

Based on the results of the initial screen, we may invite you to an interview. One of our recruiting team members will contact you to arrange this. The process may involve several interviews, initially over the phone, and then face-to-face with different members of the hiring team.

Our interviews follow a behavioral-based format. This means we’ll ask you to give us information that’s specific to your professional and educational experiences.

Hiring team members will share and discuss their input and then make their decision.

If you’re the person who best meets the requirements of the position, a member of the hiring team will get in touch to make you an offer of employment. Covance is an eVerify employer (United States only).