Senior Medical Director Clinical Development Gene Therapy and Neurology

This is what you will do :

We are looking for a Neurology and Gene Therapy medical expert who will be responsible for the clinical development of neurology assets. This position offers substantial opportunities to work with cross-functional project teams.. This role is usually assigned to 2 or more programs serving on strategic teams (e.g. disease strategy team) and providing input to strategic decisions at the TA level.

This is a therapeutic area role and is specifically designated to provide medical leadership and input to Program Teams across drug development (i.e. transitioning molecule through IND / CTA and First in Human study stage to Proof of Concept / Phase2 stage Phase 3 and regulatory approval ).

You will be responsible for :

Serve as subject medical expert and clinical development leader accountable for 2 (or more) programs including but not limited to the preparation and execution of a clinical development strategy and related documents including protocols charters statistical summary reports meeting presentations publications and clinical sections of regulatory documents.

Provide clinical development leadership for protocol execution including interaction with investigators and contributing to data review data analysis and the preparation of final clinical study reports.

Provided strategic medical guidance to phase I / II / III development programs and oversight of global patient clinical trials / trial team (s) in conjunction with Clinical Operations on assigned program(s)

Provide medical monitoring for assigned programs and assessment of safety events in conjunction with Safety teams

Represent clinical team on the cross-functional program team accountable for medical input to integrated development plan

Development of medical content for regulatory document and responses (including but not limited to pre-IND IND briefing packages and common technical documents)

Lead identification and external engagement with key opinion leaders for assigned programs including at advisory meetings investigator meetings and patient advocacy organizations

Fostering development of Medical Directors in the

Providing scientific and medical input (consultative services) to other R&D commercial translational medicine and business development functions and leads or oversees clinical activities to support due diligences

Working internally with other members of the CDP to drive program strategy and CDPs

Coordinate communications and planning bet medical functions (Global Medical Affairs Safety Clinical Operations Biostatistics Epidemiology and Medical Science) as it relates to clinical development study design execution and interpretation of results.

Driving awareness of internal and external developments (scientific clinical competitive and regulatory) that could impact the development plan including attendance at major scientific conferences participation in competitive intelligence activities and periodic literature review

Working as part of a cross-functional team with colleagues from biostatistics data management clinical pharmacology commercial regulatory and project management

You will need to have :

MD DO MBBS (or equivalent) degree with relevant clinicanl speciality for the the therapeutic area

7 years clinical research expertise in neurological diseases with pharmaceutical / CRO industry experience in drug development

Excellent written / oral communication skills

Ability to think strategically and translate strategy into tactical plans to drive outcomes

Must be adaptable able to prioritize and manmage time effectively

Willingness to take on new responsibilities and roles

The duties of this role are generally conducted in an office environment. As is typical of an office-based role employees must be able with or without an accommodation to : use a computer; engage in communications via phone video and electronic messaging; engage in problem solving and non-linear thought analysis and dialogue; collaborate with others; maintain general availability during standard business hours.

Willing to travel to scientific meetings

We would prefer for you to have :

Specialty and / or practice or development experience in Neuromuscular disease (gMG especially)

Rare Disease and / or Cell therapy experience would be a plus

Board certified in Neurology

Publications (peer reviewed) and presentations record

Experience preparing documents and attended regulatory meetings with regulatory agencies

Experience designing and completing multinational clinical trials

History of leading cross-functional teams to define clinical strategy and clinical study design

Experience supporting business development activities

Business development experience

Publication in peer reviewed journals

Working at Alexion

Were inspired to think differently to create better outcomes. By creating an unparalleled employee experience our organization is equipped to adapt and enrich employees with a productive engaging and enjoyable work experience while accelerating world-class leadership and innovation capabilities that can deliver on our mission. Each of us is accountable for delivering innovative medicines and supportive technology with integrity so we can truly understand and better the lives of people affected by rare diseases. Together we can transform lives every day The Highest Standards By operating with the highest standards of ethics and integrity we aspire to live up to the expectations of patients physicians and ourselves and to earn trust in our communities. Diversity We encourage diversity of backgrounds and ideas. We genuinely care for and respect each other working together as a high-performing team to deliver extraordinary results while embracing different perspectives. Dedication The dedication and passion of our employees enable us to stay focused on what matters most. We push ourselves to achieve the highest level of medical innovation and to redefine what it means to live with a rare -Office Hybrid This role has an expectation of working in the office a minimum of 3 days a week. When we put unexpected teams in the same room we unleash bold thinking with the power to inspire life-changing medicines. Inperson working give us the platform we need to connect work at pace and challenge perceptions. Thats why we work on average a minimum of three days per week from the office. But that doesnt mean were not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds with as wide a range of perspectives as possible and harnessing industry-leading skills. We believe that the more inclusive we are the better our work will be. We welcome and consider applications to join our team from all qualified candidates regardless of their characteristics.

We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment) as well as work authorization and employment eligibility verification requirements.

Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment training compensation promotion and other terms and conditions of employment based on race color religion creed or lack thereof sex sexual orientation age ancestry national origin ethnicity citizenship status marital status pregnancy (including childbirth breastfeeding or related medical conditions) parental status (including adoption or surrogacy) military status protected veteran status disability medical condition gender identity or expression genetic information mental illness or other characteristics protected by law.

The annual base pay for this position ranges from 280895.20 to 421342.80 USD Annual . Our positions offer eligibility for various incentivesan opportunity to receive short-term incentive bonuses equity-based awards for salaried roles and commissions for sales roles . Benefits offered include qualified retirement programs paid time off (i.e. vacation holiday and leaves) as well as health dental and vision coverage in accordance with the terms of the applicable plans.

Date Posted

19-Nov-2025

Closing Date

25-Nov-2025

Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and furtherance of that mission we welcome and consider applications from all qualified candidates regardless of their protected characteristics. If you have a disability or special need that requires accommodation please complete the corresponding section in the application form.

Required Experience :

Director

Key Skills

EMR Systems,Post Residency Experience,Occupational Health Experience,Clinical Research,Managed Care,Primary Care Experience,Medical Management,Utilization Management,Clinical Development,Clinical Trials,Leadership Experience,Medicare

Employment Type : Full-Time

Experience : years

Vacancy : 1