Clinical Research Assistant - Albany, NY

The IMA GroupAlbany, NY
9d$19 - $21Onsite

About The Position

IMA Clinical Research is seeking a Temporary Clinical Research Assistant with phlebotomy experience to support patient enrollment and study start-up activities for a new clinical trial. This is a temporary position designed to provide additional operational and patient-facing support during a high-volume enrollment period. In this role, you will assist with front desk and administrative functions while working directly with study participants, making you a vital contributor to the success of the trial. The IMA Group is an Affirmative Action/Equal Opportunity Employer Our Government Services Division supports local, state, and federal agencies and delivers professional and objective medical and psychological examinations as well as ancillary services. Our Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.

Requirements

  • High school diploma or equivalent required
  • Proficiency with phlebotomy, Microsoft Word and Excel; familiarity with CRIO and research databases preferred
  • Willingness to learn lab specimen processing and trial-related procedures with a proactive and positive attitude

Nice To Haves

  • 1 year of experience as a Medical Assistant with phlebotomy experience; minimum of 6 months in a medical office or similar setting
  • Bilingual English/Spanish preferred
  • Prior experience in clinical research or a medical setting strongly preferred

Responsibilities

  • Provide administrative support to study coordinators, including scheduling patient visits in accordance with protocol requirements
  • Assist with patient-facing study activities such as vital signs, EKGs, patient interviews, and medical record reviews
  • Maintain accurate and compliant documentation for regulatory submissions and internal reviews
  • Perform phlebotomy and manage laboratory specimen collection, processing, and shipping per study protocols
  • Answer and triage incoming research office calls, providing timely and professional assistance
  • Collaborate closely with the Clinical Research Team, demonstrating professionalism, adaptability, and strong communication skills
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