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Clinical Research Coordinator I

Company: Velocity Clinical
Location: Lafayette
Posted on: November 22, 2022

Job Description:

Job Description Job Title: Clinical Research Coordinator I Position Description: Conduct and manage clinical trials in accordance with the study protocol, GCP, and Velocity's SOPs. Position Reports To: Site Manager/Site Director Position Qualification Requirements: Education: * High School Graduate and/or technical degre Experience: * High School Graduate: minimum of 4 years requisite experience * Associate or Bachelor's degree: 1 year of clinical research experience Required Licenses/Certifications: * Phlebotomy if applicable and required by state law * Intravenous/Intramuscular dose administration and preparation if applicable and required by state law Required Skills: * Demonstrated knowledge of medical terminology * Proficient in the use of the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone. * Ability to work in a fast-paced environment * Strong verbal, written, and organizational skills * Strong interpersonal and communication skills * Ability to work as a team player * Demonstrated ability to read, write, and speak English * Ability to multi-task * Ability to follow written guidelines * Ability to work independently, plan and prioritize with some guidance * Ability to be flexible/adapt as daily schedule may change rapidly * Must be detail oriented * Demonstrated problem solving and strategic decision making ability. * Demonstrated ability to accept individual responsibility for actions taken and demonstrate professionalism when judged, critiqued and/or praised. Required Physical Abilites: * Sit or stand for long periods of time * Travel locally and nationally * Communicate in person and by a telephone * Limited walking required * Limited to lifting up to 30 pounds Position Responsibilities: * Conduct and manage clinical trials in accordance with the study protocol, GCP, and Velocity's SOPs * Implement and coordinate assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. * Develop,"coordinate,"and implement research and administrative strategies to successfully manage assigned protocols. * Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors. * Apply good documentation practices when collecting and correcting data, transferring data to sponsor/CRO data capture systems and resolving queries * Maintain confidentiality of patient protected health information, sponsor confidential information and Velocity confidential information * Ensure patient safety is upheld and all adverse events, serious adverse events, and adverse events of special interest are followed and reported in accordance with the protocol and Velocity SOPs. * Ensure all data is entered into the sponsor's data portal and all queries are resolved in a timely manner * Ensure staff are delegated and trained appropriately and documented * Understand key timelines, endpoints, required vendors, and patient population for each assigned protocol. * Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope * Promote respect for cultural diversity and conventions with all individuals. * Follows a Quality Control strategy for reviewing ones work on an ongoing basis and is prepared for monitor visits. * Other duties as assigned Print Name Signature Date Velocity Head of Department

Keywords: Velocity Clinical, Lafayette , Clinical Research Coordinator I, Other , Lafayette, Louisiana

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