Job Details

ID #46146051
Estado Dakota del Sur
Ciudad Pierre
Full-time
Salario USD TBD TBD
Fuente ICON Clinical Research
Showed 2022-10-01
Fecha 2022-10-01
Fecha tope 2022-11-29
Categoría Etcétera
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Vice President, Therapeutic Area

Dakota del Sur, Pierre, 57501 Pierre USA

Vacancy caducado!

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives.Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.That’s our vision. We’re driven by it. And we need talented people who share it.If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. Position Summary: VP, Therapeutic area Oncology/Heamatology This position will be responsible for providing input into oncology development strategies across a portfolio of early stage/FIH, up to late stage programs within solid tumors and hematologic malignancies, while providing regulatory, scientific and medical guidance. This position will partner with cross-functional stakeholders internally and externally to ensure that Clinical Development scientific and medical strategies are aligned with broader customer driven development requirements and patient needs. The ability to achieve corporate and personal objectives while maintaining the highest ethical, regulatory and scientific standards are critical components of this role. The ideal candidate should have prior oncology drug development experience in a pharmaceutical or biotech company, or recent experience in a major regulatory agency. The candidate will lead multiple cross-functional project teams and be involved in the majority of phases of drug development (preclinical through to Phase IIIa). Primary Responsibilities + Provide strategic drug development and scientific expertise to client companies + Present medical and operational capabilities to clients and develop high-level client relationships + Provide mentoring and assist with the supervision of scientific resources and project related personnel. + Support business development initiatives, including portfolio reviews + Demonstrate leadership and serve as a scientific and drug development expert resource for project teams + Support ICON’s visibility and position within the CRO industry through publications and presentations at scientific congresses Qualifications: + MD (or non-US equivalent) or MD/PhD with board certification in medical oncology and/or hematology preferred with a specialty in one or more of the following: Solid tumors, Hematology Malignancies, Immuno-oncology or Adaptive Cell Therapy + 10+ years of oncology drug development experience in biopharmaceutical industry with significant experience in oncology translational medicine/biology. + Experience in life cycle management of oncology drugs. + Thorough understanding of drug development, including working knowledge of relevant ICH and GCP guidelines and regulations + Record of significant and successful contributions to regulatory submissions, including INDs, NDA, BLAs, and regulatory agency interactions + Proven leadership ability, especially in a matrix organization + Proficiency in developing, nurturing, and managing partnerships and collaborations with external parties (including but not limited to KOLs, biopharma leaders, and the broader scientific community), + Able to work efficiently in a team oriented setting; willing and able to contribute to other work groups internally including Operations, Commercial and Regulatory + Able to successfully manage collaborations with consultants, pharmaceutical partners, and other external organizations is desirable + Aptitude and interest in serving as a subject matter expert and mentor across the organization + Excellent interpersonal, written and oral communication skills; experience delivering effective presentations to both technical and non-technical audiences + Attention to detail and strong organizational skills + Ability to prioritize and manage multiple responsibilities simultaneously Benefits of Working in ICON:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals – both ours and yours.We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans – and related benefits such as life assurance – so you can save and plan with confidence for the years ahead.But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

Vacancy caducado!

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