Clinical Research Assistant I

Clinical Research Assistant – Clinical Trials Do you have experience in clinical or laboratory settings and a passion for advancing medical research? We're looking for a Research Assistant to join a growing clinical trials organization that offers excellent development opportunities and a collaborative work environment. If you're ready to support impactful studies and contribute to the well‑being of patients, this could be the role for you! Key Responsibilities Perform a variety of clinical and laboratory procedures including vital signs, ECGs, phlebotomy, sample collection, and processing. Conduct the Informed Consent process and manage subject records. Assist in clinical data entry, transcription of source data to Case Report Forms (CRFs), and ensure compliance with Good Documentation Practices (GDP). Handle laboratory specimens, including preparation, labeling, tracking, and shipping. Support clinical operations, sample management, and subject care across various departments. Ensure adherence to clinical, regulatory, and safety standards. Required Qualifications & Experience High school diploma (or GED) + experience as a Medical Assistant, EMT, LVN, Phlebotomist, Foreign Medical Graduate (FMG), or Corpsman in a clinical or laboratory setting Ability to perform clinical procedures such as ECGs, vital signs, and sample processing. Strong attention to detail with excellent organizational skills. Initiative and problem‑solving abilities with a focus on quality and accuracy. Ability to maintain confidentiality and understand medical terminology. Strong team player with an action‑oriented mindset, great time management, and process management skills. Additional Requirements Basic Life Support (BLS) certification (required, but can be provided). GCP training (required, but can be provided). Flexibility to work across multiple shifts (morning, evening, and overnight as required). #J-18808-Ljbffr SciPro