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3 days old

Data Manager

WIRB-Copernicus Group (WCG)

General Information

Location: Bala Cynwyd, PA

Organization: ACI Clinical

Job Type: Full Time - Regular

Description and Requirements


The Data Manager (DM) manages the delivery of processes as they relate to adjudication and clinical trials within project timelines. The DM is responsible for creation, testing, and maintenance of the project database. The DM works closely with the Project Specialists to ensure case processing is performed according to project guidelines and within agreed upon timeframes. Additionally, the DM assists the Associate Data Manager with escalated issues and quality control of key documents for those projects requiring oversight.

Vaccination Requirements: 

To be considered for U.S.-based positions unless currently employed by WCG, where permitted by applicable law (including any applicable reasonable accommodation, medical or religious exemption), candidates must have received or be willing to receive the COVID-19 vaccine by start date.

Location:  Our DM will be required to work in the office 2-3 days per week, once the company opens the offices for business.  This date has yet to be determined.      

Education Requirements: 

  • BS/BA required or equivalent experience.

Qualifications / Experience: 

  • At least five (5) years of clinical data management experience in the CRO and/or pharmaceutical industry.
  • Excellent written and verbal communication skills.  Effectively communicates to a wide variety of audiences, including clients, internal project teams and senior management.
  • Strong organizational skills and ability to handle fast-paced environment.
  • Excellent attention to detail and strong analytical skills.
  • Ability to lead a technical team and define complex processes in workflows.
  • Working knowledge of Microsoft Office Suite and Adobe Acrobat.
  • Ability to handle fast-paced environment.

Essential Duties / Responsibilities:   

  • Working with technical experts and project team to implement the committee infrastructure according to the clinical trial protocol, sponsor requirements, and charter within the defined timelines.
  • Facilitating communication of project workflows among internal ACI project team, sponsors, sites, committee members, and other vendors as needed.
  • Creating project deliverables including configuration and implementation of ACIs adjudication system AIMS.
  • Creation of project documents relating to adjudication and clinical trials. Project documents may include any of the following:  Charter creation, eCRF creation, System configuration and testing, Edit specification authoring and testing, Data Reconciliation, Metric review and reporting, Standard and custom reports and/or Data Review

About Us: 

ACI Clinical provides top-tier Endpoint Adjudication and Data Monitoring Committees that deliver reliable and trusted information to support safety decisions around clinical development programs.  As the only company focused entirely on expert committees, safety monitoring and analytics, we understand every aspect of the process and what is truly needed to achieve the best results.  Our Executives are involved in current regulatory efforts shaping committee practices and we continue to build our global network of more than 750 qualified medical and statistical experts to serve as a source of committee members.  By leveraging these strong academic relationships with our proprietary technology and in-house expertise, ACI excels at designing and managing the entire committee process for safety event detection and assessment to meet any clients needs.

Categories

Posted: 2021-09-13 Expires: 2021-10-14

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Data Manager

WIRB-Copernicus Group (WCG)

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