Senior Clinical Scientist, Oncology

PhD/RN/MS

At least 5-8 years experience as a Clinical Scientist preferred with preference given to oncology clinical strategy and execution

Experience with randomized controlled trials preferred

Experience with project management, clinical research and scientific writing

Periodic travel (~15-20; includes overnight domestic and international travel to study sites, conferences, and meetings)

The

Senior Clinical Scientist, Oncology

will leverage their scientific and medical expertise in oncology to lead and execute clinical development activities for one or more assigned studies in molecular residual disease monitoring. Acting as a key leader on study teams and departmental initiatives, they will drive the development of clinical strategy, incorporating insights from the competitive landscape and aligning with the broader company vision to advance innovative solutions in oncology.

Develop study concepts, including overall study design, schedule of assessments, objectives / endpoints, and eligibility criteria. Integrate feedback from internal and external stakeholders including senior leadership, key investigators, internal stakeholders, and regulatory agencies

Contribute to authoring of the study protocol and provide critical feedback and review of supporting documents; help to respond to health authority feedback