Das ist der Job
The salary range for this position is annually (For hourly paid p
Darum lohnt es sich
What you will do Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects Typically involved in all stages of the clinical study, including identifying potential sites, performing study start-up activities such as collecting regulatory documents and supporting negotiation of contracts and budgets, training sites to collect data and report safety events, managing site activities during study maintenance, and closing down research activities at sites once the study has concluded Conduct study initiation visits (SIVs) While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements What you will bring to the role Excellent interpersonal, oral, and written communication skills in English Superior organizational skills with attention to detail Ability to work with little or no supervision Proficiency in Microsoft Office, CTMS, and EDC Systems Your experience 5+ years of experience as a Clinical Research Associate 4-year university degree or Nursing Degree Experience in Oncology is required Candidates must reside in the Central United States Willingness to travel regionally required We are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
