Ionis Brand

Associate Director, Clinical Development - Neurology

$169K–$251KFull-time · Carlsbad, CA
✓ Verified live on the employer's own system · added 15 days ago
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Mid-level · 5+ yrs exp

Requirements

Education: Doctorate

Experience: 5+ years

Skills & tools

Team LeadershipData AnalysisRegulatory SubmissionsClinical TrialsPediatric CareOperationsEmerging Risk AssessmentAdvocacy
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Full job description

about the opportunity to have meaningful impact on patients in need, we invite you to apply and join us. Experience and contribute to our unique culture while you develop and expand your career!

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. Near-term responsibilities focus on leading key aspects of Ionis-sponsored clinical trials, clinical data analysis and interpretation, communication of project information and risks, and contributions to regulatory submissions, publications, and presentations.

Over time, the role may have opportunities to contribute to broader clinical development strategy and clinical trial design.

This position sits within the neurology franchise (including rare diseases). The primary focus will be neurology, including neuromuscular diseases, neurodegenerative diseases, and rare pediatric neurogenetic disorders. This position can be fully onsite, remote, or hybrid.

For remote employees, periodic travel to Ionis' headquarters in Carlsbad is expected, approximately once per quarter.

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.

- Lead and/or contribute to analysis of clinical trial data and the preparation of manuscripts, abstracts, posters, and presentations.

- Maintain up-to-date clinical and technical expertise in the relevant therapeutic areas by reviewing scientific literature, attending key scientific and technical meetings, and partnering with internal medical, research, and commercial teams.

- Contribute to broader department and corporate objectives, as needed.

- Other duties as assigned.

REQUIREMENTS:

- The successful candidate is self-driven and effective both as an individual contributor and a flexible team player. They anticipate and identify risks/problems and excel at problem-solving. They bring a practical, hands-on, "can-do" and time-conscious approach, motivated by doing the things today that will deliver transformative treatments to patients with high unmet need tomorrow.

- PhD, MD or PharmD with 5+ years of pharma/biotech experience in clinical development

- Experience in neurology, rare diseases, and/or pediatrics is highly desirable

- Significant experience with cross-functional collaboration (e.g., clinical operations, regulatory, stats, data management)

- Experience with protocol/protocol amendment writing and CSR writing

- Experience authoring and/or leading Clinical Study Report (CSR) development. Experience contributing to NDA filings is highly desirable

- Experience leading cross-functional data reviews, experience with elluminate is preferred

- Experience supporting FDA Pre-Approval and BIMO inspections is highly desirable

- Experience managing vendors/committees (e.g., DSMBs) is highly desirable

- Outstanding interpersonal and communication skills, with the ability to flexibly relate to diverse internal and external stakeholders and to build strong, positive relationships across development, research, commercial, and senior leadership

- Ability to thrive in a fast-paced, innovative environment

- Strong attention to detail and quality combined with the ability to make timely decisions and drive execution

- Willingness to engage in thoughtful, interrogative debate around key issues and, when appropriate, to constructively challenge the status quo

Please visit our website, http://www.ionis.com for more information about Ionis and to apply for this position; reference requisition # IONIS004080

Ionis offers an excellent benefits package! Follow this link for more details: Ionis Benefits

Full Benefits Link: https://ionis.com/careers#:~:text=Highly%20competitive%20benefits

The pay scale for this position is $168,820 to $250,502

NO PHONE CALLS PLEASE. PRINCIPALS ONLY.

Ionis Pharmaceuticals, Inc. and all its subsidiaries are proud to be EEO employers.

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