Clinical Research Associate

Location: Charleston
Posted on: June 23, 2025

Job Description:

Job Description: · CRAs primary responsibility is to build relationships with Principal Investigators, study co-ordinators, pharmacists, and all relevant site trial personnel to ensure the efficient, expedited, and smooth management of clinical trials. · Foster internal and external customer relationships to ensure focus on efficient, timely and productive project delivery as per study requirements and timelines. · In collaboration with the In-house Clinical Research Associate (IHCRA) and Regulatory Start-Up Associate (RSA), prepare site essential documents, and support the ethics and regulatory submission and approval processes as needed. · In collaboration with Regulatory Start-up (RSU) Team, understand the requirements of applicable local and international regulatory requirements as relevant to specific clinical trials. · Ensure recruitment of participants as per the site target. Drive site recruitment and engagement initiatives and prepare site-specific recruitment plan(s) and update as required. · Monitoring of investigational sites as per ICH GCP (Monitoring) and the Clinical Monitoring Plan (CMP) for each study. This includes all monitoring visit types across all phases of a clinical trial including Site Selection, Site Initiation, Site Monitoring and Site Close Out, unblinded pharmacy visits, and co-monitoring visits. Visits can be conducted either onsite or remote as per CMP. Experience and Qualifications · Graduate in a clinical or life sciences-related field. Relevant experience/qualifications in allied professions may also be considered. · Must have good time management skills, attention to detail, be able to work well in a team, and be computer literate. · Preferably experience of working in the research, pharmaceutical industry or a related field per job level as follows: · At least 2-3 years of Clinical Research Associate experience in the Clinical industry. · Excellent interpersonal and team skills with a genuine commitment to contributing to the development of innovative treatments EEO: Mindlance is an Equal Opportunity Employer and does not discriminate in employment on the basis of – Minority/Gender/Disability/Religion/LGBTQI/Age/Veterans.

Keywords: , Savannah , Clinical Research Associate, Science, Research & Development , Charleston, Georgia