Medical Director, Clinical Development Genomic Medicine Neurology

This is what you will do:

We are looking for a Neurology medical expert who will be responsible for the early clinical development of genomic medicine neurology programs. This position offers substantial opportunities to work with cross-functional project teams and career advancement in the fast-moving area of genomic medicine.

You will be responsible for: 

• Medical Expert accountable for the early clinical study design, protocol development from concept to final implemented protocol for assigned programs 

• Protocol execution including interaction with investigators, and contributing to data review, data analysis and the preparation of final clinical study reports.

• Strategic guidance to phase I/II development programs and oversight of global 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 interacted 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 external engagement for assigned programs at advisory meetings,  investigator meetings and patient advocacy organizations

• Contribute to the medical assessment of business development opportunities for rare neurology programs

You will need to have:

• MD, DO, MBBS (or equivalent) degree with relevant clinicalspeciality for the the therapeutic area 

• Deep clinical and clinical research expertise inneurological diseaseswith 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 andmanage time effectively 

• Willingness to take on new responsibilities and roles 

• Interest in career progression and ability to take on a more senior roles in 1-3 years

• 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.

We would prefer for you to have:

• Clinical experience in genetics therapeutics preferred

• Previous clinical trial experience as medical monitor in industry setting

• Safety medical monitoring and reporting experience

• Protocol development experience

• Understanding of regulatory requirements related to clinical trials

• Basic statistical knowledge

• Board Certification in Neurology

• Business development experience

• Publication in peer reviewed journals

At Alexion, you will find a collaborative culture that encourages innovation and a diverse environment where your contributions are valued. You will have the opportunity to be at the forefront of rare disease research and make a meaningful difference in patients' lives.

Working at Alexion

• We’re 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 disease.

  In-Office Hybrid

  This role has an expectation of working in the office 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. In-person working give us the platform we need to connect, work at pace and challenge perceptions. That’s why we work, on average, a minimum of three days per week from the office. But that doesn’t mean we’re not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.