Associate Research Coordinator at Renstar Medical Research

Ocala, Florida, United States -

Full Time

Start Date

Immediate

Expiry Date

21 Jun, 26

Salary

0.0

Posted On

23 Mar, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Participant Visit Management, Study Coordination, Protocol Execution, Clinical Procedures, Source Documentation, Data Query Resolution, Sponsor Communication, CRO Communication, Study Material Preparation, Multitasking, Prioritization, Attention To Detail

Industry

Research Services

Description

Description Renstar Medical Research is seeking an Associate Research Coordinator to support our clinical trial team. This role provides increased responsibility in participant visit management, study coordination, and protocol execution while working closely with experienced Clinical Research Coordinators and investigators. This position is ideal for Clinical Research Assistants or research professionals who are ready to take the next step toward Clinical Research Coordinator responsibilities. Requirements Key Responsibilities Conduct and assist with participant visits in accordance with study protocols Coordinate participant scheduling and protocol-required visits, including imaging and other study-related procedures. Perform protocol-required clinical procedures and assessments once trained and delegated Maintain accurate source documentation and ensure activities are documented according to study requirements Coordinate with QC/Data Specialists to resolve data queries and ensure documentation supports study data. Communicate with sponsors and CRO representatives regarding protocol procedures when appropriate. Prepare study materials and documentation for participant visits and monitoring visits Support the operational management of assigned studies throughout the study lifecycle. Qualifications Clinical research experience preferred (e.g., Clinical Research Assistant or similar role) Healthcare or patient-care experience in a clinical setting Strong understanding of clinical research processes and Good Clinical Practice (GCP) principles Strong attention to detail and documentation accuracy Ability to work effectively across multidisciplinary clinical research teams Strong multitasking and prioritization skills in a multi-trial research environment Education Associate or bachelor’s degree in health sciences, biological sciences, psychology, nursing, or a related field preferred. Equivalent clinical research or healthcare experience may be considered in lieu of formal education. Career Development Renstar Medical Research is committed to developing clinical research professionals. This role is part of a structured career pathway: Clinical Research Assistant ? Associate Research Coordinator ? Clinical Research Coordinator

Responsibilities

The Associate Research Coordinator will conduct and assist with participant visits according to study protocols, managing scheduling and required procedures like imaging. This role also involves performing clinical procedures, maintaining accurate source documentation, and coordinating with data specialists to resolve queries.