At least 2 years of clinical research experience as a clinical research coordinator and experience working in a medical center or private practice.…

Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol(s) in order to be able to answer all……

Experience preparing sources, reviewing and conducting Informed Consent process with subjects, EDC entry and query resolution, and completing all study specific……

The ideal candidate will possess certification such as an RN, LPN, MA, phlebotomy, or similar, prior clinical research experience, and have a strong desire to……

Oversees the development of clinical trial protocols; participates in the development of the overall clinical plan, drafts protocols, collaborates on……

1+ year of experience in research/clinical investigations/studies required (participant recruitment, data collection, data entry, informed consent, scheduling,……

Answering and triage of research office calls. Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful……

Assist in research planning, design and implementation including the development of standard operating procedures (SOPs), research forms and source……

In this role, you will complete tasks related to the preparation, execution, and close-out of clinical research studies under general direction of Clinical……

Ideal candidates will possess Bachelor's degree in the sciences and/or clinical experience. Employee will be trained to follow Good Clinical Practices and……

This position will establish, develop, and implement recruitment plans, and conduct thorough phone screens and in-person interviews discussing medical history……

Education: Bachelor’s degree preferably in Science or related field. Maintains compliance with Good Clinical Practice; Clinical Safety Data Management, 21 CFR,……

This includes but is not limited to administrative tasks including checking participants in/out, answering phones, data entry, as well as adherence to protocol……

BS in nursing, pharmacy or other related science or combination of equivalent education preferred. The CRC II's responsibilities is to screen, enroll and follow……

Associate or an allied health degree in life science or related area or one year of relevant experience, or combination of education and relevant experience.…

Must have had independent clinical license for at least three years and a solid body of knowledge of clinical theory. CPR / First Aid / Narcan Training.…

Responsible for maintaining registry for assigned investigators; including following FDA regulations and GCP standards, data collection, data entry, data……

Serving as back up to front desk staff, laboratory staff and regulatory when requested. You should have demonstrated mastery of foundational educational……

Must have a bachelor’s or master’s degree in a life science related area. Studies involve clinical stem cell and platelet rich plasma work, photobiomodulation,……

Prefer a RN with a NC Nursing license. This position will participate in evaluating, planning, and executing patient subject care in clinical research studies.…

Supports the implementation of approved site plans as outlined in the strategic plan and provides leadership through implementation.…

Serving as a liaison and resource for external partners, including clinical sites, clinical research organizations, and laboratory vendors.…

Currently holds an unencumbered RN license with the State Board of Nursing where the practice of nursing is occurring and/or possess multistate licensure if in……

Serving as the primary liaison between clinical study sponsors, patients, and VTV staff regarding study protocol requirements and communicates clinical study……

IATA and/or Safe-T-Pak certification for shipment lab specimens and/or dry ice. CPR and first aid certification. Evaluate clinical lab reports.…

Previous clinical trial experience required. Medical background, phlebotomy and computer skills are required. All patients are currently required to wear a mask……

Assists in the development and implementation of recruitment strategies to increase patient randomization for clinical trials.…

1+ years of experience working in a biology, cell biology, or other life-sciences laboratory setting. Master’s degree (MA/MS/MBA) in Biology, Cell or Molecular……

Medical and scientific knowledge: A Clinical Research Coordinator doesn’t have to be a doctor, pharmacist or scientist, but they do need to have some knowledge……

Basic Life Support certification (Online BLS certifications, those without a skills assessment component, are not sufficient to meet the BLS requirements).…