Clinical Research Coordinator

company

Our client is a Pharmaceutical Manufacturing company that offers a full service clinical research site-network. Their technology solutions use artificial intelligence to match patients to clinical trials at a level of precision and speed not previously possible. They facilitates new connections between physicians, their patients, and clinical trial opportunities to accelerate patient recruitment.

qualifications

• Associate degree or higher
• Clinical Research (3+ years)

• 1+ years of experience in ANY of the following:
  • Phlebotomy
  • Performance of Vital Signs
  • Medical History Collection
  • Administering EKGs

overview

Summary: We are looking for experienced candidates with medical backgrounds and excellent interpersonal skills for the position of Clinical Research Coordinator (CRC). This role is responsible for the successful conduct of clinical trials under the oversight of the principal investigator. The CRC will be responsible for both clinical and administrative duties related to the conduct of clinical research at the site. Clinical Research Coordinator Requirements: • Upwards of 3 years’ experience as a clinical research coordinator, preferably on phase II & III studies • Currently trained or willing to be trained in phlebotomy, performance of vital signs, medical history collection, and administration of EKGs • Attention to detail • Exceptional interpersonal and customer service skills • Outstanding written and verbal communication • Excellent organizational skill • Willingness to continually self-educate A Plus (but not required) • Fluency in Spanish Clinical Research Coordinator Responsibilities: • Abide by local, state, GCP, ICH and FDA guidelines and regulations for the conduct of clinical trials. • Oversee the smooth running of clinical trials at site in collaboration with study investigator(s) and other team members • Complete all required organization and study specific training in timely manner, including attendance at offsite investigator meetings • Supervision and training of site research site staff, including study coordinators, research assistants and lab technicians • Participate in the planning and conduct of research participant recruitment efforts • Conduct the proper consenting of research participants • Collecting source obtained from research and transcribe into case report forms. • Perform medically qualified clinical procedures such as vital signs, EKG, and phlebotomy • Process study labs per requirements • Provide clinical research training and mentoring to study team. • Provide responsive and diligent collaboration with sponsor/CRO study teams, including prompt resolution of queries and other action items. • Monitoring research participants to ensure adherence to study participation and maintain compliance • Perform regular inventory checks and ensure the necessary supplies and equipment for a study are in stock and in working order. • Engaging with subjects and understanding their concerns