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Ionis Pharmaceuticals, Inc.
Associate Director, Clinical Development - Neurology
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What they do
A Clinical Director directs and manages a medical practice, clinic, hospital, or other clinical setting. Organizes and manages of staff physicians, policy implementation, and ensures that standards for medical care are communicated and maintained.
$166,864 / year median in the U.S.
+16% projected growth
Job Description
Associate Director, Clinical Development
- Neurology Ionis Pharmaceuticals, Inc.
- 3.8 Carlsbad, CA Job Details $168,820
- $250,502 a year 4 days ago Qualifications Biotechnology Medical writing Experimental data reports Pharmaceutical company experience Scientific protocols Clinical data report preparation Cross-functional collaboration Pharmaceutical research experience Cross-functional communication Scientific reports Full Job Description Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases.
ASSOCIATE DIRECTOR, CLINICAL DEVELOPMENT
NEUROLOGY SUMMARY:
The Associate Director, Clinical Development- Neurology provides clinical development leadership and scientific expertise to one or more project teams, supporting the successful design and execution of development plans for Ionis' investigational assets.
RESPONSIBILITIES
Serve as the clinical lead for assigned studies, representing Clinical Development in internal and external interactions and helping ensure successful execution of a high-priority Phase 3 program by: Developing and maintaining excellent working relationships with investigators and clinical trial teams Delivering high‑quality scientific presentations on company technology, investigational agents, and clinical study issues to investigators and site staff Providing guidance and/or training for external personnel involved in Ionis clinical studies Performing ongoing review of clinical study data and operational progress Identifying emerging risks and partnering with the project team to proactively manage and mitigate them Lead and/or contribute to the writing and review of key clinical documents for regulatory submissions (e.g., study protocols, Investigator's Brochures, IND submissions, Clinical Study Reports). Engage internal and external stakeholders (e.g., key opinion leaders, advocacy organizations, regulators) to obtain advice and feedback that informs development plans, trial designs, and study results. Communicate project information- including study progress, risks, plans, and recommendations
- clearly to project teams and Ionis leadership.