Associate Director, Oncology Clinical Science

HybridPalo Alto, California, United StatesClinical Development and Clinical Operations OncologyFull time1308 Description This role is involved in the design, monitoring, and data analysis of the Company’s oncology clinical trials.
As such, the Associate Director, Oncology Clinical Scientist is an important and visible member of the Oncology team.
Key Responsibilities Provide input to protocol design, provide oversight of clinical data (entry by sites, data completeness/accuracy working closely with ClinOps/Biometrics/Data Management teams), and support site and subject retention in clinical trials alongside the Medical Monitor(s) Develop and maintain up to date slide presentations for internal meetings related to the clinical trial(s) Ensure successful completion of documents (including protocols, investigator brochure, safety monitoring plan, site training materials, clinical study report, health authority responses, standard operating procedures, etc.
) with cross-functional team members Represent Clinical Development on study teams and cross-functional teams as appropriate or as delegated by the Medical Monitor(s) Ensure consistent use of language and criteria across multiple oncology projects (including partner studies) Ensure study integrity and track accumulating clinical data in real time Analyse, evaluate, and support accurate interpretation and reporting of clinical data Maintain up-to-date knowledge of relevant science, medical information, good clinical practices, and regulatory guidance Able to mentor and manage clinical scientists or interns (assigned as direct reports) within Clinical Development Collaborate with—and serve as a clinical research resource for—cross-functional colleagues to optimize product development Cultivate relationships with investigative sites, clinical consultants, and key opinion leaders to represent the interests of the company Contribute to corporate strategic and organizational initiatives Complete assigned tasks thoroughly, accurately, and on time Adhere to rigorous ethical standards Travel up to 20% domestically and internationally for scientific meetings Requirements Knowledge, Skills and Experience Advanced degree e.
g.
Ph.
D.
, Pharm.
D.
, equivalent OR at least 8 years of relevant work with direct involvement in clinical trials Strong track record of scientific and clinical inquiry Understand statistical concepts and clinical trial design Possess excellent communication skills (both written and verbal) Learn quickly, follow complex directions under pressure Multi-task while remaining organized and attentive to detail Work hard, be a trustworthy and collaborative team player Take initiative and solve problems of moderate complexity Demonstrate sound judgement in terms of handling complex, confidential, and regulated information Lead both directly and by example At least 5 years of experience with clinical trial design and execution At least 5 years of pharmaceutical industry experience Experience with regulatory submissions and interactions preferred Estimated compensation 185-200K/year DOE Benefits Medical insurance Vision insurance Dental insurance 401(k) Paid maternity leave Paid paternity leave Commuter benefits Disability insurance