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VP Disease Area Lead, Specialty, Clinical Sciences

Employer
GSK
Location
Collegeville, Pennsylvania; San Francisco, California; Waltham, Massachusetts
Salary
Competitive
Closing date
Jun 21, 2021

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Discipline
Health Sciences, Medicine
Job Type
President/CEO/Director/VP
Organization Type
All Industry, Pharma
Site Name: UK - Hertfordshire - Stevenage, UK - London - Brentford, USA - California - San Francisco, USA - Massachusetts - Waltham, USA - Pennsylvania - Upper Providence Posted Date: May 21 2021 GSK seeks an outstanding clinical development leader to join our Clinical Sciences organization as the VP, Disease Area Lead, Specialty. This represents a unique opportunity to accelerate our expertise in new disease areas, and to contribute to building our industry-leading Development and Clinical Sciences organization. As a senior physician or clinical scientist, you will oversight of the clinical development strategies across all relevant programs after phase 1 through to registration across our growing Specialty portfolio, including Neurosciences, Infectious Disease, Rare Disease, Cardiovascular, Metabolic and Renal. Reporting to Marek Honczarenko, SVP & Head Clinical Sciences, you'll have direct line function responsibility for all Clinical Sciences staff within Specialty (approx.10 direct reports, and up to 25 indirect reports) including physicians and clinical scientists. You'll work in a matrix role to support Early Development Teams (EDTs) for preparing Specialty programs for entry into clinical development and Medicine Development Teams (MDTs) for driving clinical strategy for late stage assets. As a core member of the Protocol Review Forum (PRF), you will ensure the highest level of quality for all Specialty clinical protocols. Playing a pivotal role in collaborating with the Head of Clinical Sciences, your role will be to set up disease area strategies, ensuring the quality and robustness of the medicine vision, clinical development plans and the integrated evidence plans for programs in order to support the development, approval, commercialization and patient access to differentiated medicines with proven value. You will also be accountable for Medical Governance for clinical programs. VP DAL Key Responsibilities in Detail Single point of accountability for disease area strategy developed with input from internal GSK leaders & colleagues and from academic thought leaders, research leads, regulatory authorities, investigators and patient groups. You will provide Disease Area Clinical Leadership, Disease Area Expertise, Patient and Prescriber Insights at the disease level, including opening potential new areas of interest and optionality for alternative development pathways, enabling smart risk-taking by decision-makers for assets with indications in the disease area. To drive innovation in design of clinical development plans and study protocols within the disease area, accessing world-class expertise through external and internal collaboration, harnessing digital, technological and statistical tools and with specific accountability to support early stage programs in the disease area by bringing in disease insights and clinical research expertise. Provide Medical Governance with specific accountability for managing and mentoring clinical staff in the disease area line and ensure proper training and compliance with internal and external policies, guidance, laws and codes. To develop and maintain Clinical Development Excellence in the disease area through talent identification, recruitment, development and retention, to support the pipeline and marketed portfolio. To ensure quality of clinical deliverables within the disease area including all documents and submissions including clinical data, through methods such as peer review, knowledge sharing/management, and standards and compliance. To act as Data Steward of the clinical data for the disease area (may include multiple assets) To manage resourcing of Clinical projects within the disease area across the assets in scope including portfolio projects and programs (encompassing Research stage projects, Development projects (from Phase II onwards) and business development/due diligence activities). Basic qualifications MD or PhD with expertise in a relevant Specialty TA (eg Infectious Diseases, Cardiovascular, Neuroscience) You will be a recognized expert in Specialty & clinical research, demonstrating depth and breadth of knowledge and understanding of scientific, medical, regulatory and digital data environments, practices and requirements. Skilled in leveraging your expert knowledge for scientific, technical, clinical and regulatory strategic thinking, problem solving and decision making in the evolving healthcare and digital data environments. Demonstrated ability to lead and inspire teams and allocate resource strategically and according to portfolio priorities. Preferred qualifications Proven ability to manage and develop self and work collaboratively with others to deliver innovative and creative results and solutions. Broad understanding of local and global Pharmaceutical industry, competitive landscape, how end-to-end life and revenue cycles operate Strong people management, leadership and motivational skills Superior stakeholder management skills, across scientific, academic, regulatory and political communities to identify and achieve mutual goals for the well-being of patients and our communities Leadership Characteristics A talented and experienced leader motivated by the desire to make a difference in patients' lives. Excited by challenging goals and positively impacting the progression of medicines of value to patients that provide the adequate return to the business. Proven ability to think and plan uniquely and strategically, to work with members of other functions within a matrix environment. Intrigued by innovation, creativity and new opportunities to learn Energized by delivering high standards through collaboration and motivating others across the organization Passionate about developing others into future leaders Committed to maintaining the highest compliance standards Closing date for applications: 20th June 2021 *LI-GSK If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US). 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, color, 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. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit GSK's Transparency Reporting For the Record site.

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