General Information

Location: Bala Cynwyd, PA, Remote

Organization: ACI Clinical

Job Type: Full Time - Regular

Description and Requirements

ACI is looking to hire a Data Manager to join our team! Our Data Manager will support projects by managing the delivery of processes as they relate to adjudication and clinical trials.  We have a flexible work schedule and opportunity to work from home, not to mention working with a fantastic team of Data Managers!  


  • 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.

  • Assist with the configuration and implementation of ACI’s adjudication system, AIMS.

  • Create project documents relating to adjudication and clinical trials.

  • Configuration of our systems and conduct testing

  • Edit specification authoring and testing

  • Perform data reconciliation

  • Review metrics, data, and analyze reports


  • BS/BA required or equivalent experience.

  • At least five (5) years of clinical data management experience in the CRO and/or pharmaceutical industry.

  • Excellent written and verbal communication skills to effectively communicate 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 work with a technical team and define complex processes in workflows.

  • Skilled in using Microsoft Office Suite and Adobe Acrobat.

  • Ability to handle fast-paced environment.

About us:

ACI Clinical, a member of the WCG Clinical family, is a specialty provider of clinical trial committees and clinical trial advisory services. ACI maintains deep involvement in several public-private thought leadership efforts to improve the quality and effectiveness of clinical trials by enhancing data integrity for regulators and the scientific community to drive efficiencies in clinical research and enable more informed decision-making.