Job description
Mantell Associates are partnered with a leading CRO, in their search for a Clinical Research Associate.
Clinical Research Associate - Responsibilities:
Build relationships and oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff
Drive productivity by developing patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines
Ensure compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s)
Monitor the completeness and quality of Regulatory Documentation and perform site document verification
Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports
Clinical Research Associate - Requirements:
Bachelor’s or equivalent degree preferably in Biological Science, Pharmacy or other health/science related discipline
Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology
Perform all clinical monitoring activities independently
Strong interpersonal, written, and verbal communication skills within a matrixed team
The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s)
Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word
Outstanding interpersonal, teamwork, organisational, and time management abilities
Mantell Associates is a specialist Pharmaceutical and Life Sciences headhunting firm. For more information on this role, please contact us at +1 (786) 485 1298.