Detail

Salary
negotiable
Location
Cambridge, UK
Posted by: Astra Zeneca
16 Nov
334 Views
15 Jan EXPIRED

Head of Clinical Development – Neuroscience

Cambridge, UK
Job Description

In this hands-on, head of clinical development, physician role within neuroscience we are looking for a creative physician who can bring their experience to lead a team of physicians and take ownership for the clinical development of the neuroscience portfolio of large and small molecules.

We look for entrepreneurial thinking and the ability to provide medical leadership to defined operating procedures, and includes study design and execution, development of clinical protocols, medical monitoring, and timely reporting of study outcomes. If this sounds like you, then please apply now!

Neuroscience at Astrazeneca

With a rich heritage and a research and development focus on specific aspects of neurodegenerative diseases, analgesia and psychiatry, AstraZeneca continues to push the boundaries of science in neuroscience in collaboration with other innovative partners across industry and academia.

Join a small, agile business unit, which runs semi autonomously within AstraZeneca and has a biotech culture, which is continuing to evolve and grow with new products and talent joining year on year!

Role accountabilities:

As a member of the Neuroscience team, you will lead the conduct of a portfolio of projects in neuroscience including:

  • Leadership of development, including plans and approach to the projects, ensuring efficient execution and delivery from candidate to end of Phase 2, including contribution to preclinical development enabling first-in-human (FIH) studies.

  • Leadership and personal growth of a team and function.

  • Represent the clinical and medical aspects of neuroscience assets to governance committees and work with colleagues in the late-stage development organization and with co-development partners to facilitate transition of products into pivotal trials.

  • Medical and scientific contribution into design and implementation of clinical protocols, data collection systems (eCRF and related platforms), digital tools, data analysis including the statistical analysis plan.

  • Accountable for planning, conducting and evaluating clinical trials and supervising cross functional team members to ensure successful trial delivery.

  • Review and interpret study results. Analyze and synthesize clinical data for publication, and international regulatory filings. Author clinical publications or provide input into communication and publication development.

  • Establishing close collaboration between company experts.

  • Support assets transitioning from the pre-clinical portfolio into clinical development, with a key role in defining the early clinical development.

  • Selection and management of collaborators and vendors including academic groups, CROs, and technical expertise or services within AZ.

  • Contribute to development of disease area strategies that integrate discovery research with clinical approaches to proof-of-concept in appropriate patient segments.

  • Evaluate and recommend licensing and acquisition opportunities and participate in due diligence activities.

  • Actively participate in co-partnering discussions providing your expertise to joint steering committees and/or clinical co-development teams.

Job ID Reference
1630
Desired Skills & Experience

Essential criteria

  • MD, MBBS, MBChB qualification, or equivalent.

  • Significant experience of leadership in a commercial environment is crucial, most likely achieved within the setting of a pharmaceutical company, biotech or contract research organisation.

  • Proven track record of medical proficiencies and decision-making capabilities achieved in a clinical practice setting (at least to the level of senior resident or consultant/attending physician in a relevant medical speciality).

  • Excellent communicator and collaborative team leader.

  • Handle complexity - you will integrate and analyse non-clinical and clinical data as well as data/input from multiple internal and external functional areas. Synthesis of previous clinical data and ongoing medical safety data is required. Capacity to manage multiple tasks/programs with competing deadlines/priorities is essential.

  • Able to operate relatively independently in medical, safety and clinical development tasks with minimal supervision. Once direction is provided, must identify the challenges, generate solutions (or options) and either implement a recovery plan, or advance through relevant functions for further advice.



Company
  Gaithersburg, Maryland, USA
  www.astrazeneca.com
AstraZeneca is an exciting global, innovation-driven biopharmaceutical company. We’re inspired by what science can do. Driven by the desire to meet unmet patient needs in our core therapeutic areas. Bold in our thinking. Proactive in pursuing discoveries beyond imagination. At sites across the world, we bring teams together in a spirit of collaboration to turn great ideas into life-changing medicines – strengthening our product portfolio and harnessing the potential of a pipeline across all stages of the drug development process.
You’ll be part of a team that’s rolling back the frontiers of science to turn yesterday’s impossible into the normal of tomorrow. So, if you share our focus and passion, join us and make a difference to patients – and in return, we’ll help you develop way beyond what you thought possible.
  Workplace
 Cambridge, UK