Acclinate Inc. Clinical Research Diversity Coordinator Birmingham, AL · Full time

We are seeking a Clinical Research Diversity Coordinator who will serve as a liaison between Acclinate, research sponsors, and clinical study sites/teams. This individual will be responsible for leading and coordinating efforts to engage potentially eligible diverse research participants in communities of color.


Responsibilities include:

Developing strong relationships with research sponsor study teams and corresponding clinical trial sites

Communicating the importance of diverse representation to clinical trial sites and ensuring investigators and site staff have clear understanding of the diversity objectives and engagement plans

Partnering closely with research sponsors, sites, Acclinate’s Medical & Community Engagement Specialist, and Acclinate’s Director of Community to identify and employ strategies to engage potentially eligible diverse participants; evaluating processes and identifying issues related to access and engagement of diverse patient populations

Contributing to execution of effective trial awareness and pre-screening strategies for each trial

Monitoring the development and communication of outreach plans and the external clinical trial diversity engagement program; providing guidance for course correction as needed

Keeping all internal and external stakeholders up-to-date on the progress of diversity engagement plans

Managing project milestones and proactively addressing deficiencies

Attending and providing information at weekly/monthly client teleconferences/team meetings with research sponsors and/or sites

Assisting Project Manager with the preparation of information for inclusion in reports to research sponsors.

Ideal characteristics:

High integrity, fortitude, creativity, curiosity, and positive/innovative approach to problem solving

Excellent communication skills --- professional, personable

Organized, with the ability to manage multiple tasks simultaneously in a hands-on manner, adjusting to issues as needed in a dynamic and deadline-driven environment

Ability to prioritize and effectively anticipate and respond to issues as they arise

Forward-thinking in ways of scaling relationships and data across other studies and community

Proficient in MS Office, Zoom, and Slack with willingness to learn other systems


Clinical Research or Clinical Operations experience preferred, but not required



Contact: Camille Pope, PharmD, Chief Medical Lead – [email protected]