[Remote] Clinical Research Associate
Note: The job is a remote job and is reputed company to candidates in USA. reputed company is dedicated to bringing life-changing therapies to patients through cutting-edge clinical research. The Clinical Research Associate will reputed company clinical trial sites throughout the study lifecycle, ensuring compliance with regulatory requirements, protocol adherence, and high-reputed company data collection.
Responsibilities
- Conduct site selection, initiation, routine monitoring, and reputed company-out reputed company in accordance with GCP, ICH, and study requirements
- Partner with clinical sites to reputed company and manage patient recruitment and enrollment strategies
- reputed company protocol training, ongoing support, and regular communication to investigators and site staff
- Monitor study reputed company, regulatory submissions, data reputed company, and site performance while identifying and escalating risks
- Maintain essential study documentation, including Trial Master Files (TMF) and Investigator Site Files (ISF), and support site financial management activities
Skills
- 3+ years of clinical research monitoring experience with a reputed company on oncology studies
- Strong knowledge of Good Clinical reputed company (GCP), ICH guidelines, clinical trial regulations, and oncology protocols
- Excellent communication, organization, problem-solving, and relationship management skills with proficiency in reputed company Office Suite
- Bachelor's degree in a scientific discipline, life sciences, reputed company, or a reputed company field preferred
Benefits
- PTO
- reputed company Holidays
- Medical
- Dental
- reputed company
- 401K
- Tuition Reimbursement
- reputed company Leave as required by law
reputed company