Sr Clinical Development Director (Cardiovascular), Open to flexible working

Location
Stevenage, Brentford
Salary
£Competitive
Posted
25 Sep 2020
Closes
11 Oct 2020
Ref
265162
Contract Type
Permanent

Programs in Speciality Medicine are a key part of our Clinical Sciences (Clinical Development) organization. Comprising a dynamic & collaborative community of clinical development physicians and scientists across Infectious Disease, Nephrology, Cardiovascular, Metabolic, Neurosciences, and Rare Diseases, we are driving scientific innovation to deliver the next generation of transformational medicine for patients.

We're seeking a Sr Clinical Development Director/Clinical Development Lead (CDL) for our evolving cardiovascular programs in Speciality. This is an exciting opportunity for a CDL to oversee the creation and execution of clinical development strategies for an important component of the GSK portfolio. You will be accountable for the creation of the clinical strategy and oversee a clinical team accountable for trials to execute the strategy. In addition, you'll be the key internal expert for emerging opportunities for business development and in early phase development in cardiovascular and related disease areas. You will be well versed in emerging trends and opportunities in multiple disease areas. This role offers you the opportunity to utilize advanced scientific and statistical principles and digital technology in collaboration with your peers to help build GSK's emerging pipeline and to advance your career, both within Specialty and across Clinical Sciences.

Job Purpose and Key Responsibilities:

  • Providing integrated and innovative clinical development strategy to support the creation and management of the Integrated Evidence Plan (IEP), including the Clinical Development Plan (CDP) for an asset in development
  • Strategic influence: Integrating scientific rationale, regulatory requirements, product development plan and commercial goals to optimize clinical study designs aligned with the IEP and CDP
  • Generating the data and evidence required to evaluate a medicine's potential efficacy, safety profile, key areas of product differentiation and value to patient in the shortest possible timeframe
  • Establishing expeditious clinical development timelines, incorporating key decision points and Go/No Go criteria for the CDP
  • Developing and maintaining relationships with program counterparts in Commercial, Research, Regulatory, Clinical Operations and Statistics.
  • Contributing to and partnering on the development of strategic initiatives, specific Business Development activities and various organizational initiatives in Clinical Development
  • Playing an key role in the development of Clinical Sciences staff via coaching and mentoring and potential direct line management

Scientific Leadership, Direction and Strategy:

  • Employs visioning and strategic thinking to provide expert guidance of disease/therapeutic area specific strategy for a drug(s) or program(s). Manages selected clinical development projects for products/franchise of compounds
  • Serving as a clinical point of contact for senior management and senior level matrix teams, both internally and externally for an asset(s) in development
  • Partnering, positively interfacing, and influencing across a diverse range of scientific external experts (e.g. regulators, payors, CROs, consultants, investigators) in order to deliver integrated clinical development strategy, which align to the business strategy and achieves mutual goals related to patient need
  • Integrating inputs from across disciplines (scientific, clinical commercial, regulatory) to contribute to the Medicine Profile. Accountable for the clinical components of the Medicine Profile.
  • Accountable for risk/benefit of the asset. Makes decisions which balance risk/benefit at the project level with clear understanding of impact on study/project indication approvals; takes action to mitigate risk where appropriate
  • Assessing and predicting when therapies designed for one patient population/indication can be used in alternative scenarios to broaden potential patient benefit
  • Anticipating problems and proactively seeking input from other teams' members/functional lines within R&D. Uses scientific/operational expertise to solve study and/or project related problems
  • Accountable for the evaluation of clinical study/program probability of technical success (PTS)

Study & Program Design and Evidence Generation:

  • Drives the end to end integrated clinical development strategy that is appropriately resourced to achieve regulatory approvals, reimbursable medicines, and successful lifecycle management
  • Leads clinical development discussions at regulatory interactions and clinical components of the submissions (i.e. IND, NDA, BLA, MAA) including briefing documents, presentations, addressing questions and responses
  • Provides effective leadership support / oversight of evidence generation activities to assure patient safety and study delivery
  • Delivers value and access insights to inform medical strategy, expand market access and to address unmet patient need

Creating Innovative Scientific and Technical Solutions:

  • Overcomes obstacles by experimenting with and adopting new ways of working including digital tools and technology
  • Responsibility for implementation of innovative methods and processes within clinical development and gains stakeholder support; encourages others to think differently and come up with business solutions

Why you?

Basic Qualifications:

 

  • MD, PhD or PharmD degree
  • Extensive experience in clinical drug development with an understanding of multiple diseases, the underlying biology and potential therapeutic targets as well as current and future potential treatment options
  • Extensive clinical training and/or applicable clinical research experience; understanding of clinical development planning and running clinical trial from concept study idea to publication.
  • Demonstrated experience managing complex projects and working collaboratively with multiple stakeholders regarding new strategies to ensure consistent communication
  • Proven ability to maximize and integrate genetic data to advance disease understanding and inform and guide clinical development plans
  • Thorough understanding of clinical research methodology and biostatistics principles, to facilitate innovative and efficient clinical trial design, and clinical development plans with clear data- decision rules
  • Demonstrated experience using new learning and digital tools to create innovation in other areas
  • Expertise in inductive and deductive reasoning, statistics, and in providing mechanisms to interpret and analyze highly complex information including digital content

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

  • Board Certification/Eligibility in Cardiovascular Disease
  • Significant experience in leading line and matrix teams with a strong reputation of inspiring and motivating high performance
  • Demonstrated track record in cardiovascular drug development, particularly heart failure

Why GSK?

Our values and expectations are at the heart of everything we do and form an important part of our culture.

These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As GSK focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities:

  • Agile and distributed decision-making - using evidence and applying judgement to balance pace, rigour and risk, governance and control, managing ambiguity and paradox.
  • Managing team performance.
  • Creating a performance culture and driving results, prioritisation, execution, delivering performance.
  • Setting strategic direction and leading on-going organisational transformation.
  • Building a resilient organisation. Building strong relationships and collaboration in service of common goals, engaging the organisation and building trusted external networks for mutual benefit.

*LI-GSK

Closing date for applications: 11 October 2020

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