Vacancy caducado!
This individual will be responsible for conducting and managing subject research visits at clinic by following protocols, checklists and Standard Operating Procedures (SOPs). Responsibilities include:
Supports, manages, facilitates, and coordinates the day-to-day research activities at the Research Site under the supervision of Principal Investigator
Conducts clinical research subject visits daily by closely following the trial specific protocol in accordance with GCP and FDA guidelines
Completes basic clinical procedures such as phlebotomy, ECGs, pulmonary function tests, obtaining blood pressure, attaching monitoring devices and all other allowable procedures as delegated by Principal Investigator
Process / Centrifuge / Spin / Prepare blood specimens as collected for study visits
Prepares for and conducts initiation visits, monitor visits, answering questions and resolving issues in a timely manner. Prepares for and conducts study closure visits
Meets with representatives from sponsoring pharmaceutical firms and their designees or in-house staff for initial orientation to studies and for review of study records
Familiarizes potential subjects with the details of the study through phone contacts and personal interviews
Contacts / Calls CHEAR potential subject community / database about interest in studies
Keeps the internal research database up to date and keep all study staff advised of changes and updates
Manages multiple projects and meets deadlines while paying close attention to detail and accuracy
Works well as a member of the clinical research team by positive, professional, courteous and timely written and verbal communication with appropriate team members
Sits at front reception desk to meet and address patients, delivery people or anyone else as needed
Skills and experience:
International MD or Bachelors Degree
Strong communication skills both written and verbal
Ability to fluently speak, read and interpret Spanish desirable, but not required
Professional attitude
Prior experience as Clinical Research Coordinator desirable, but not required
Working knowledge of GCP (Good Clinical Practice), FDA and IRB guidelines
Strong computer and analytic skills, including MS Office (Word, Excel, Outlook)
Vacancy caducado!