About this opportunity
Neurocrine Biosciences lists this Senior Medical Director, Clinical Development, Neurology opportunity in san diego, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
About the Role
We are seeking an experienced and strategic Senior Medical Director, Clinical Development – Neurology to provide medical leadership across clinical development programs within our neurology portfolio. This role is responsible for driving clinical development strategy and leading the design, execution, interpretation, and communication of Phase 1–3 clinical studies in collaboration with cross‑functional teams. The successful candidate will serve as a key medical leader, partnering closely with Clinical Operations, Regulatory Affairs, Biostatistics, Drug Safety, Translational Medicine, Research, and Medical Affairs to advance innovative therapies through development.
Your Contributions
Lead clinical development strategy for assigned neurology programs and provide medical leadership across multiple clinical studies
Serve as Clinical Lead and primary medical representative on cross‑functional program teams
Design and oversee Phase 1–3 clinical studies, including study concepts, protocols, amendments, medical monitoring plans, and clinical development plans
Drive program‑level clinical decision‑making and contribute to integrated development strategies that support regulatory and commercial objectives
Partner with Clinical Operations to ensure high‑quality execution of clinical studies in compliance with applicable regulations, Good Clinical Practice (GCP), and company procedures
Provide medical oversight for ongoing clinical trials, including safety review, adverse event assessment, and benefit‑risk evaluation
Collaborate with Translational Medicine and Research colleagues to identify and implement biomarkers and other strategies to support development objectives
Build and maintain productive relationships with investigators, key opinion leaders, patient advocacy groups, and external collaborators
Lead analysis, interpretation, and presentation of clinical data to internal governance committees, scientific audiences, and external stakeholders
Support regulatory interactions and contribute to the preparation of regulatory submissions and health authority communications
Mentor and influence cross‑functional teams through scientific expertise, strategic thinking, and collaborative leadership
Contribute to portfolio assessments, business development evaluations, and other strategic initiatives as needed
Requirements
MD or DO (or equivalent) degree in a relevant clinical specialty for the therapeutic area required
4+ years of clinical experience with broad bio/ pharmaceutical/CRO industry experience in drug development OR accredited residency training and board certification preferred
Board certification in Neurology strongly preferred
Clinical development experience in movement disorders strongly preferred
Experience serving as a Clinical Lead or leading program‑level clinical development activities
Experience supporting late‑stage clinical development and registrational studies
Prior experience working with regulatory agencies and contributing to regulatory submissions
Experience in migraine, neurodegenerative diseases, or related neurological therapeutic areas is desirable
Deep expertise in clinical drug development and clinical research strategy
Demonstrated ability to independently drive program‑level clinical development decisions and influence cross‑functional stakeholders
Strong understanding of study design, clinical execution, safety assessment, biostatistics, data interpretation, and regulatory requirements
Proven ability to translate scientific and clinical insights into actionable development strategies
Outstanding communication, presentation, and stakeholder management skills
Strong leadership capabilities with experience influencing matrix teams and collaborating across functions
Demonstrated success managing interactions with investigators, CROs, consultants, and external partners
Knowledge of Good Clinical Practice (GCP), regulatory procedures, and investigational drug development
Ability to operate effectively in a fast‑paced, highly collaborative environment
Benefits
The annual base salary is expected to range from $301,100.00 to $411,000.00. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of the role, job duties/requirements, and relevant experience and skills. In addition to base salary, this position offers an annual bonus with a target of 35% of earned base salary and eligibility to participate in an equity‑based long‑term incentive program.
Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.
EEO Statement
Neurocrine Biosciences is an EEO/Disability/Vets employer. We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don’t line up to exactly what we have outlined in the job description.
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Worksite address
san diego, CA, 92189, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.