What are the responsibilities and job description for the Clinical Trial Associate position at LanceSoft?
Clinical Trial Associate Overview : The Clinical Trial Associate is responsible for assisting with the coordination and implementation of clinical trials. This role will work closely with the Principal Investigator (PI) and other members of the research team to ensure that clinical trials are conducted in accordance with Good Clinical Practice (GCP) guidelines and regulatory requirements. Responsibilities : Assist with the development and implementation of clinical trial protocols Recruit and screen potential study participants Obtain informed consent from study participants Schedule and coordinate study visits Collect and manage study data Monitor study participants for adverse events Report adverse events to the PI and Institutional Review Board (IRB) Maintain accurate and complete study records Communicate with study participants, study staff, and regulatory authorities Assist with the preparation of regulatory submissions Qualifications : Bachelor's degree in a relevant field such as nursing, biology, or public health 1-2 years of experience in clinical research or a related field Strong understanding of GCP guidelines and regulatory requirements Excellent communication and interpersonal skills Ability to work independently and as part of a team Proficiency in Microsoft Office SuiteWork Location : Remote OR Hybrid if in proximity to Richmond, VA (2-3 days per week on site)Work hours : 8-5 Mon-FriOn Call : NoExtension : LikelyContract to Hire : PossibleTravel : NoInterview Process : 2 video interviews']
