Exceptional opportunity to join a leading nationwide healthcare services organization in their corporate office in Houston as a Project Manager for Oncology Clinical Trials.
 
SCOPE:  Responsible for overall organization and administrative project management of clinical research initiatives.
 
RESPONSIBILITIES:
· Maintain a working knowledge of the status of clinical research programs including business, financial, and clinical activities.
· Facilitate quality improvement programs including timelines and quality of research data.
· Implement research trials and ensure successful education of clinical research staff.
· Develop study implementation processes and tools with industry sponsors and contracting organizations.
· Serve as a point of contact for sponsors and provide information to physicians and research staff regarding clinical trials.
· Maintain trial documentation and files including database of participants in studies.
· Prepare and coordinate pre-qualification visits, medical quality and FDA audits.
 
QUALIFICATIONS:
· RN or Bachelor’s in a Biomedical Science.
· 2+ years clinical research experience.
· Prior oncology clinical research experience preferred.
· Understanding of FDA and other regulations regarding the conduct of clinical research.
· CCRC or CCRA certification preferred.
 
Local Houston candidates only.  Please respond with your resume as a Word document.