DM Clinical Research, the largest privately-owned research management organization in the Houston area, is looking for an experienced Site Manager. This role will be responsible for coordinating site operations.
Responsibilities and Duties:
Completing DMCR-required training, including GCP, IATA, and NIH.
Ensuring compliance with research protocols by reviewing all protocol requirements to confirm implementation of appropriate methods, practices, and procedures for all clinical activities.
Managing team of Study Managers, CRCs, RAs, and administrative staff; monitoring their day-today tasks and holding them accountable.
Conducting staff onboarding training along with 90-day and annual employee evaluations.
Training staff on all aspects of study protocols and study manuals as applicable.
Training laboratory staff on study protocols.
Collaborating with both internal and external cross-functional stakeholders.
Identifying potential roadblocks and helping to shape solutions to meet the needs of patients, caregivers, and investigator study sites.
Coordinates multiple projects with competing priorities and deadlines as needed based on clinical trial protocol directives and study volume.
Identifies departmental needs, supplies, staffing and equipment goals to continually improve the research process within the established guidelines of the institute.
Monitors adherence to protocols and study timelines.
Facilitates daily operations of all clinical research programs.
Monitoring ongoing clinical trials, including coordinating with study monitor, communicating with study sites, and monitoring of study data and consumables.
Being prepared for and available at all required company meetings and monitor visits for their assigned protocols.
Assisting in creation of e- source documents for their assigned protocols at their respective site(s)