The successful candidate will have the skills necessary to thrive in a fast-paced environment, as well as the ability to build a team and successfully manage the future growth of his/her function as the Company expands. Particularly important skills include intelligence, logical thinking, ability to prioritize, can-do attitude, the ability to adapt quickly to changing business conditions, and strong interpersonal and team building skills.

Responsibilities:

• Supervise and mentor CRAs and other operational personnel
• Work with the Director and Medical Monitor to develop protocols and all documents required to initiate and conduct clinical studies, including informed consent forms, investigator brochures, case report forms, study procedure manuals, etc;
• Liaison with external service providers
• Develop and manage the clinical project team to meet clinical trial timelines consistent with the companys goals
• Select study investigators and evaluate adequacy to perform research and meet study timelines
• Creates and negotiates clinical trial site budgets
• Manage studies to meet enrollment goals

Qualifications:

• Relevant experience in clinical trial execution
• Phase 3 experience is a plus and highly desired
• Oncology experience
• Strong knowledge of GCP and ICH guidelines
• Must be willing to travel as required for the project; estimated travel ~20%

Education and Experience:

• Bachelors degree plus six or more years of pharmaceutical clinical research experience strongly preferred; RN degree or a degree in a healthcare related field or the life sciences is desirable but not mandatory

We offer a diverse workforce with a competitive salary and benefit package.
Please apply using the linked application form:
Application Form