Dir, Epidemiology Pipeline; TA-Oncology

Benefits

Qualifications

• •Subject‑matter expert in oncology clinical trials
• •Basic knowledge of statistical programming languages (e.g., SAS, R, Python)
• •Excellent written and oral communication and presentation skills
• •Strong interpersonal communication and team‑oriented skills
• •Demonstrated leadership and technical skills
• •2 more items(s)

Responsibilities

• •Serves as a scientific resource for RWLP management, senior management, and other functions within the company, providing expertise in multiple scientific areas
• •Works hand‑in‑hand with RWLP management, business development, and operations personnel to develop and win global business opportunities; helps to lead the development and delivery of project proposals, bid defenses, and represents capabilities presentations
• •Provides overall scientific oversight of selected projects, responsible for meeting or exceeding customer expectations for timelines, budgets, quality, and overall satisfaction
• •Coordinates with the project manager to oversee the scientific aspects of study start‑up and ongoing study management; leads the development of and/or peer‑review of essential study documents including the protocol, case report forms, statistical analysis plan, study management plans, and interim/final study reports
• •Facilitates scientific advisory boards for safety studies and produces scientific reports, manuscripts, abstracts, and presentations
• •Maintains a strong working understanding of clinical and epidemiological practice guidelines, clinical research models, protocol designs, real‑world research development trends, and regulatory expectations; develops trainings for the organization to enhance familiarity with epidemiologic study designs and applicable guidelines
• •Responsible for the continued building of organizational capacity, improvement of scientific and operational processes, and methodologies for non‑traditional site management tasks (e.g., remote or central monitoring approaches, minimized regulatory document collection), integrated technology solutions, and standard operating procedure development and maintenance
• •Works collaboratively across the organization to develop business opportunities in the area of post‑marketing safety commitments and/or risk management; develops and recommends techniques to improve productivity, increase efficiencies, cut costs, and maintain state‑of‑the‑art practices
• •Develops collegial relationships with sponsors, thought leaders, and clinical investigators
• •Develops abstracts, provides podium presentations, and leads authorship of articles, manuscripts, and other publications to promote the company’s services
• •7 more items(s)