Associate Dir/Sr. Mgr, Clinical Research Science R&D | Innovative Oncology/I-O Therapies | Exciting & Growing Biopharma | Boston Area
This is an exciting opportunity to join an attractive and rapidly growing global biopharma company with a very impressive and diverse early-late stage oncology/I-O development pipeline. As a key member of the Global Clinical Science/Development Team, you will work on the company’s biggest/highest profile program in oncology and be an integral part of collaborating in key discussions that will influence the strategic scientific and operational decisions that will impact the successful clinical development of these novel assets/drugs.
ATTRACTIVE FEATURES ABOUT THIS COMPANY & OPPORTUNITY:
Impactful Role on High-Profile I-O Program: You will be an integral part of developing an extremely promising new I-O cell therapy discovered by one of the most respected and revered Cancer Academic Research & Medical Centers in the world.
Enjoy the Best of Both Worlds: Enjoy the minimal layers of management and swift decision making of a biotech culture, while also enjoying the financial stability and the financial strength of an established global biopharma (i.e. more financial and human capital resources, more assets, better compensation and benefits, etc).
Strong Collaborations / Financial Strength/ R&D Spend: Join an oncology company with a track record of establishing multiple collaborations with top oncology academic research centers, and with other innovative biotech companies too in a highly competitive marketplace. This company has strong revenues, profits, cash & market cap that invests heavily in its annual R&D.
Excellent Hiring Manager: Report into a very highly-regarded and well-respected hiring manager/Department Head (whom we know very well and have an excellent relationship with).
Competitive Compensation/Benefits: This company offers a very competitive compensation package and an extensive benefits package (strong LTI, 401(k), employee stock purchase plan & much more).
RESPONSIBILITIES IN A NUTSHELL:
Lead the scientific and medical review of clinical data across multiple studies in immuno-oncology and participate in the creation, maintenance, and execution of clinical development plan that will result in the regulatory approval of the compound in multiple regions.
Represents Clinical Science on US/EU Development Teams.
Participates in a multi-disciplinary, matrix team ensuring that scientific issues are appropriately considered with respect to highly complex data findings.
Supports the Global Development Team to ensure that the US/EU Development Team activities are aligned with the global strategy.
Provides critical evaluation of the development strategy to maintain a state-of-the-art development plan that is competitive and consistent with the latest regulatory requirements, proactive identification of challenges, and development of contingency plans.
Contributes to high impact global decisions: monitoring and interpreting data from ongoing internal and external studies and making recommendations that impact regional and global development such as “go/no go” decisions or modification of development plans or study designs.
Contributes to the development of protocol synopsis, obtaining scientific and corporate review committee approval including presentation and defense of the Synopses during review committee meetings, review and approval of documents related to study protocols.
Provides scientific contributions and overall content approval of written responses required by IRB / Ethics Committees and critical study training meetings.
Responsible for review of study data, interpretation of results and communication of study conclusions within the company.
Influences establishment of strategy for assigned compound, and the development of documents required to outline the company’s positions on research programs or regulatory applications.
Interacts directly with research division based on pertinent clinical and development expertise to provide knowledge / understanding of market environment.
Contribute to Clinical Development Plan, protocol, IB, eCRF, SAP, CSR development, as well as other critical study documents.
Six Campus Drive | Suite 301 | Parsippany, New Jersey 07054 USA
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About CORNERSTONE SEARCH GROUP
Cornerstone, recognized by Forbes as one of the "Top 100 Executive Search Firms in the U.S." and by Hunt Scanlon as one of the "Top 50 Healthcare & Life Sciences Executive Search Firms," is a Life Sciences Executive Search firm that helps companies based around the world, ranging from startup biotechs to Top 10 Pharmas, to find, attract, and hire talent for their US and globally-based leadership positions (CxO and xVP levels) as well as their critical Director/SD/ED-level roles.
Keywords: Program, Asset, Oncology, Hematology, Immuno-Oncology, Cancer, IND, NDA, Protocol, Clinical Development Plan, CDP, Clinical Study Report, CSR, Filing, Submission, Regulatory, Clinical Research, Clinical Development, Global, Clinical Science, R&D, Scientific, Clinical Research Scientist, Director, Lead, Cell Therapy, CAR T, immunology
EDUCATION & REQUIRED EXPERIENCE:
Advanced scientific degree (PhD, PharmD or MSc) is required.
4+ years of relevant clinical research and/or clinical development experience ideally within the pharmaceutical/biotech or related industry.
Sufficient grounding in the principles of the scientific method of the immune system, coupled with experience in oncology/cell therapy drug development to lead internal and external projects across the spectrum of R&D (early and late phase).
Internal Number: bcsBH2778acrp
About Cornerstone Search Group
CORNERSTONE is a pharmaceutical specialty recruiting firm located in the heart of New Jersey's Pharmaceutical Corridor. We help our clients hire experienced pharmaceutical professionals from the Staff through Management (VP/Director) levels for Full-Time and Contract positions. We provide our professional recruiting services on a Contingency basis and, when warranted, on a customized Exclusive, Retingency or Retained basis as well.