Job Description

Job Description:

• Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials.
• Assists with patient care in compliance with protocol requirements. May disburse investigational drug and maintain investigational drug accountability. Participates in data collection, entry, and reporting for the subjects.
• In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings.
• Participates in required training and education programs as well as monitoring and auditing activities. May work directly with sponsors. May participate in scheduling monitoring and auditing visits, as well as interact with the monitors/auditors while onsite.
• Assists with collection and maintenance of regulatory documents in accordance with USOR SOPs and applicable regulations.

Qualifications:

• Associates degree in a clinical or scientific related discipline required, bachelors degree preferred
• One year of experience in a clinical or scientific related discipline, preferably in Oncology
• Previous Clinical Research Experience Required

Business Experience:

• Experience with Microsoft Office
• Experience working with Physicians preferred

Specialized Knowledge/ Skills:

• Must have excellent communication skills
• Excellent organization skills
• Strong ability to multi-task
• Excellent time management skills
• Must have strong interpersonal skills to be able to interact with multiple people on multiple levels
• Must have a high attention to detail
• Must be able to work in fast-paced environment
• May be responsible for basic clinical assessments

Job Tags

Similar Jobs