Clinical Development Lead

Clinical Development Lead (CDL) is responsible for the overall Japan clinical development plan for assigned projects. CDL ensures studies are designed to fit Japan specific requirement and situation from clinical regulatory and operational perspectives. CDL is accountable for planning and execution of assigned clinical studies and leads communication with the external stakeholders (e.g. investigators regulators KMEs academic societies). CDL is accountable for clinical contents of local study documents (e.g. protocols IBs ICFs) and regulatory documents (e.g. briefing books responses to regulatory queries CTDs).

• Develops Integrated Development Plan (IDP): accountable for Japan clinical development strategies
  • Provides RDPT with necessary information including disease landscape SOC KMEs and competitor situation in Japan
  • Works collaboratively with the Project Team and PDC members to integrate the scientific rationale regulatory requirements operational feasibility product development plan and commercial goals to build a solid strategic framework for the Japanese components of the IDP
  • Leads clinical development strategy discussion.
  • Ensure that a Japanese strategic plan is fully aligned with a global strategy and is fully understood by a project team
• Leads clinical studies in assigned projects as an owner of the studies.
  • Ensures the study protocol is applicable to Japanese medical practice and manages local protocol amendment if necessary.
  • Ensures that the resources and budget necessary for the successful execution of the trial are secured in collaboration with the CTM.
  • Accountable for study feasibility in Japan
  • Accountable for CRO and vendor selection and study budget.
  • Proactively identifies study level risks and drives execution of risk mitigation strategies
  • Accountable for solving study related issues in Japan including management of AEs in collaboration with Study Medical Director and Safety Physician.
  • Maintains study quality
  • Understands the protocols and educate study team members
• Leads medical and scientific discussion as a Biogen Japan clinical representative with investigators and KMEs.
• Serves as a local clinical representative in regulatory interactions in Japan
  • Prepares and/or reviews clinical contents of regulatory submission documents and responses to clinical regulatory inquiries.
  • Participates in regulatory consultations and discussions
• Establishes and maintains scientific reputation in academic societies by participating in major scientific conferences and making scientific presentations/publications.

Qualifications:

• Science background and education (Bachelors Degree or equivalent) MD/PhD/PharmD preferred
• Strong clinical credentials and/or drug development experiences in the therapeutic areas combined with strong grounding in scientific research.
• Clinical development experience within in biopharmaceutical industry (at least 3 years in product development).
• Experience working with regulatory agencies (PMDA experience preferred)
• Ability to lead scientific discussion on mechanisms of new research approaches clinical endpoints protocol design and data interpretation
• Established or has ability to establish peer level relationships with therapeutic area opinion leaders worldwide
• Demonstrated leadership and team building skills as well as the ability to perform effectively in a dynamic environment
• Demonstrated strategic and critical thinking
• Excellent communication skills (oral and written) with business level English and excellent organizational skills
• Ability to lead directly and by influence including strong problem solving conflict resolution and analytical skills

We are a global team with a commitment to excellence and a pioneering spirit. As a mid-sized biotechnology company we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning growth and expanding their skills. Above all we work together to deliver life-changing medicines with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds cultures and perspectives make us a stronger and more innovative company and we are focused on building teams where every employee feels empowered and inspired.Read onto learn more about Biogen.

All qualified applicants will receive consideration for employment without regard to sex gender identity or expression sexual orientation marital status race color national origin ancestry ethnicity religion age veteran status disability genetic information or any other basis protected by federal state or local law. Biogen is an E-Verify Employer in the United States.