Clinical Development Lead - Oncology Cell & Gene Therapy, Open to flexible working

Location
Stevenage, Hertfordshire
Salary
£Competitive
Posted
15 Mar 2021
Closes
11 Apr 2021
Ref
282936
Contract Type
Permanent

Do you want to be part of a highly regarded and rapidly growing Oncology R&D team focused on improving the lives of cancer patients? If so, the Clinical Development Lead - Oncology, is an excellent opportunity to explore.

GSK is expanding the Oncology Clinical Development organization and we are seeking experienced professionals to join our exciting journey. GSK Oncology has a commitment to the discovery and development of new oncology therapies with the life-changing potential of helping patients with cancer, specifically in four areas of cancer research: Cancer Epigenetics, Immuno-Oncology, Oncology Cell & Gene Therapy and Synthetic Lethality.

The Clinical Development Lead (CDL) - Oncology, will be an integral part of one of the 4 mechanistic platforms as the single point of accountability for the Clinical Development Plan (CDP). The CDL provides clinical and strategic leadership to the program.

Key elements of the role include:

  • A key member of the Medicine Development Team representing Clinical Development
  • Provide a single Clinical Development accountability at the program level into Medicine Development Team, Early Development Team, Medical Affairs, Integrated Evidence, Publications, and Global and Regional Commercial functions
  • Accountable for overall benefit: risk of a clinical program.
  • Lead cross-functional Clinical Matrix Team and provide clinical leadership, Oncology Clinical Development expertise, and customer insight for the program
  • Act as the single point of accountability for oversight of multiple clinical development plans (CDPs), disease strategies, molecules and/or indications from end-to-end, as well as associated clinical trial programs and studies.
  • Guide direct reports to ensure cross-functional integration, coordination, collaboration, and alignment to enable effective and efficient CDP execution.
  • Contribute strategic guidance and highlight clinical considerations to inform portfolio development strategies, individual study design and conduct, combination strategies, and disease area strategies
  • Interpret complex clinical data and identify trends for clinical and regulatory documents consult on safety analyses, and responses to health authority queries
  • Prepare for governance discussions in close collaboration with cross-functional Medicine Development Leader (MDL) and other business lines
  • Manage a team of physicians and/or scientists and allocate resources across the program accordingly

Additional responsibilities include:

  • Author and/or review abstracts, presentations and manuscripts for accuracy of clinical data and content.
  • Contribute to the establishment of standards for clinical documents and data review processes across Oncology Clinical Development.
  • Participate in interpretation of data analyses of clinical trial results and support development of clinical study reports
  • Lead preparation of clinical sections of relevant regulatory filings (IND, study reports, NDA, annual reports, etc.)
  • Serve as program clinical expert for internal and external collaborators, investigators, consultants, and contract resources
  • Lead and provide clinical support for investigator and consultant meetings (e.g., investigator meetings, clinical advisory boards)
  • Lead recruitment, hiring and training for direct report team roles
  • Provide direct reports with ongoing coaching, development and leadership; includes holding regular staff meetings, check-ins and 1:1 meetings

Why you?

 

Qualifications:

We are seeking a professional with the following qualifications and skills to achieve our goals:

Basic Qualifications:

  • Physician-scientist with strong understanding of translational disease biology or ability to design innovative trials based on emerging biomarkers and clinical outcome measures
  • M.D. or M.D./Ph.D. (or ex-US equivalent) with Board Certification in a relevant specialty; oncology or hematology
  • At least 8 years pharmaceutical or relevant scientific/medical/clinical experience required, with at least 5 years of Oncology clinical development experience
  • Established track record of scientific publications and presentations
  • Experience leading matrix teams with a strong reputation of inspiring and motivating high performance.
  • Cross-functional medicine development knowledge and business acumen.
  • In depth knowledge of medical and drug terminology and a sound foundation in pharmacology.
  • Demonstrated ability to produce written scientific communications with clarity, accuracy and rigor and in compliance with GSK control documents governing disclosure, publication and principles of scientific exchange.
  • Robust knowledge of Oncology treatment guidelines, therapeutic competitive landscape, clinical development process and drug approval process in major regions.
  • Broad experience in the principles and techniques of data analysis, interpretation and clinical relevance (e.g., ISS, ISE, competitor data, etc.)
  • Comprehensive understanding of product and safety profiles
  • In-depth knowledge of medical aspects of GCP (Good Clinical Practice), ICH (International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use), FDA, EMEA, NICE and other relevant guidelines and regulations

Preferred Qualifications:

  • Experience with cell therapy or bone marrow transplant
  • Background in immunology
  • Clinical development experience in one of GSK's 4 mechanistic platforms
  • Highly effective communication skills; able to present complex data, design, strategy to groups at all levels of the organization.
  • Ability to adjust behaviours and priorities based on changing environment and dynamics.
  • Ability to engage in, and contribute to, Oncology Clinical Development Culture and broad GSK environment with confidence, impact, integrity and professionalism.
  • Demonstrated understanding of the detection, investigation, assessment and prevention of adverse effects of medicines on patients.
  • Highly developed negotiating and influencing skills. Ability to influence others to make sound decisions from a clinical perspective.
  • Demonstrated track record of quality decision making and creative problem resolution in critical situations, based on assessment of all relevant supporting and conflicting information/factors and understanding of the wider context.

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, rigor and risk
  • Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution.
  • Continuously looking for opportunities to learn, build skills and share learning.
  • Translating strategy into action - a compelling narrative, motivating others, setting objectives.
  • Building strong relationships and collaboration, managing trusted stakeholder relationships internally and externally.
  • Leadership (expertise, self-awareness, high performance behaviours and ability to execute the assigned role) in a matrix and line environment
  • Embedding a culture of individual empowerment across the broader study team

GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, colour, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

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