Clinical Sciences Associate Director
23 hours ago
We are seeking a highly experienced and skilled Clinical Sciences Associate Director to join our team at Novartis Group Companies. This is a key leadership position that will be responsible for leading cross-functional teams in the design, execution, and delivery of complex global early-phase oncology trials.
Key Responsibilities- Lead global cross-functional Clinical Trial Teams (CTTs) to ensure all trial deliverables are met, setting stretch goals, promoting realistic planning and timelines, and presenting actionable alternatives to accelerate timelines.
- Proactively lead risk mitigation discussions, risk management, and implementation at the trial level, responsible and accountable for forecasting and managing overall study budget(s) in collaboration with key partners.
- Develop and implement study-level operational execution plans in partnership with key cross-functional partners, independently leading the clinical protocol development process in collaboration with the Medical Lead and other line functions.
- Contribute to the medical/scientific input given for the development of study-related documents and processes, and contribute to the development of clinical sections of study-level regulatory documents.
- Lead the ongoing medical/scientific review of clinical trial data across assigned studies in collaboration with the medical expert and key line functions, and partners on data analysis and data interpretation, including safety trend analysis, signal detection, development of first interpretable results, reporting clinical study results in Clinical Study Report (CSR), and internal/external publications.
- Bachelor's degree in life science/healthcare required; advanced degree or equivalent education/degree in life sciences/healthcare preferred (PhD/MD/PharmD/Masters).
- Approximately 8+ years' experience in clinical trials/development with 3+ years leading cross-functional teams, ability to lead multiple complex clinical trials concurrently.
- Strong understanding of oncology/hematology and demonstrates high learning agility, proficient in clinical trial methodology with an emphasis in early clinical development.
- Strong operational project and program management experience with an emphasis in early clinical development, including excellent planning, prioritization, problem-solving, and organizational skills.
- Demonstrated capability to interpret, discuss, and represent trial-level data, demonstrated knowledge and ability to confidently drive complex collaborations through unpredictable circumstances and higher-paced changes.
- Radioligand therapy (RLT) experience preferred.
We offer a competitive compensation package, including a salary range of $174,400.00 - $261,600.00, a sign-on bonus, restricted stock units, and discretionary awards, as well as a full range of medical, financial, and/or other benefits, including 401(k) eligibility and various paid time off benefits.
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. We do not discriminate in recruitment, hiring, training, promotion, or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.
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