Clinical Trials:

• Participate in the design, development, implementation, and execution of clinical trials and protocols.
• Coordinates, and maintains all regulatory documentation including IRB submissions and approvals, study revisions and amendments, safety and progress reports.
• Performs data management design, entry, and maintenance.
• Provides direct patient care as per the requirements of the clinical research studies. 
• Ensures proper collection, processing, and handling of study specimens.

Administrative:

• Develops study standard operating procedures, compliance forms, and tracking documents.
• Recruit, screen, and enroll study participants who meet research criteria. Maintain telephone, electronic, and in-person contact with subjects. 
• Develops and provides study materials, education, and training materials to patients, family members, and clinical staff to ensure patient safety and adherence to protocols.
• Provide administrative support to the COHC team as needed.
• Other duties as assigned.

Knowledge, Skills, andAbilities: 

• Knowledge of clinical research practices, preferably in oncology and/or integrative medicine care.
• Ability to communicate effectively, both orally and in writing.
• Strong organizational, administrative, and interpersonal skills.
• Ability to work on multiple projects.
• Ability to handle confidential and sensitive information.