人妻少妇乱子伦无码视频专区

Clinical Research Coordinator

Highly Competitive
  1. Permanent
  2. Clinical Research Associate (CRA)
  3. United States
Miami, USA
Posting date: 29 Aug 2025
66824

Clinical Research Coordinator - Permanent - Miami

人妻少妇乱子伦无码视频专区 is seeking a Clinical Research Coordinator to join a dynamic team in Miami. This position offers an opportunity to contribute to impactful neurology research while maintaining compliance with Good Clinical Practice (GCP) and other applicable regulations.

Primary Responsibilities:

The successful candidate will coordinate participant care, manage trial data, and collaborate with investigators, clinic staff, sponsors, and CROs to facilitate effective research activities. They will also oversee the performance of clinical trials, ensuring alignment with regulatory standards and organizational goals.

Skills & Requirements:

  • Experience in clinical research or a relevant clinical role.
  • Certification as a CCRC or CCRP is preferred.
  • Strong organizational, leadership, and communication skills.
  • Ability to multitask, think critically, and maintain attention to detail.
  • Proficiency in computer systems and knowledge of medical terminology.
  • A positive, professional attitude with strong interpersonal and customer service skills.
  • Commitment to supporting organizational goals and maintaining industry knowledge through training and meetings.

The Clinical Research Coordinator's responsibilities will be:

  • Coordinate clinical trials under the supervision of a Principal Investigator, adhering to FDA, GCP, and protocol guidelines.
  • Identify and address potential issues or inconsistencies in trial processes.
  • Communicate protocol-related matters with study teams, sponsors, and CROs.
  • Collect and review participant health and demographic information to determine eligibility.
  • Perform clinical tasks such as vital signs, ECGs, phlebotomy, and specimen processing.
  • Maintain accurate and timely documentation, including EDC data entry and query resolution.
  • Dispense investigational products and ensure proper record-keeping.
  • Educate participants and their families about study protocols and clinical trials.
  • Conduct quality control checks and collaborate with QA teams as needed.
  • Support recruitment efforts by participating in planning meetings, providing updates, and coordinating with recruitment teams.

If you are having difficulty in applying or if you have any questions, please contact Nico Kohlwes at n.kohlwes@proclinical.com

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

人妻少妇乱子伦无码视频专区 is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. 人妻少妇乱子伦无码视频专区 is acting as an Employment Agency in relation to this vacancy.

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