Director, Clinical Science – Oncology | public biotech with big pipeline | New Jersey: RETAINED SEARCH

Cornerstone Search Group
Published
May 29, 2020
Location
Greater New York City Area, United States
Category
Job Code
caCRSoncNJ2760
Contact Email
tfascia@cornerstonesg.com

Description

Director, Clinical Research Scientist - Oncology | Well-funded Public Biotech | large self-discovered pipeline | New Jersey: RETAINED SEARCH

SUMMARY: Cornerstone Search Group has been retained by a uniquely attractive Oncology biotech for a Director, Clinical Research Scientist (CRS) position that is newly-created due to the advancement of their large self-discovered pipeline featuring multiple assets entering late-phase global development. This is a “best of both worlds” opportunity because you will simultaneously enjoy the benefits of a smaller, entrepreneurial environment while having the comfort and security of working for a well-funded public company with a large, diverse, self discovered pipeline addressing a range of solid and liquid tumor types. Furthermore, our client has in place strategic collaborations with several top pharma companies.

As a key member of the Clinical Development team, the CRS will work closely with Clinical Development Asset Leads and the CMO, all of whom have strong industry experience, to ensure that all phases of clinical development, including the design and implementation of clinical protocols and development plans, are achieved successfully and expeditiously.  Unlike at larger pharmas, this role provides the opportunity to make a strategic and scientific impact in a growing development organization on current and future clinical programs as this company has a prodigious clinical and pre-clinical pipeline.

The ideal candidate will help to build clinical expertise and be able to collaboratively design, plan, implement, analyze, and report clinical studies. This is a unique opportunity to expand your knowledge in the scientific and research aspects in oncology across multiple areas working on several assets, through day-to-day activities and close interactions with the R&D organization.

TITLE: Director, Clinical Research Scientist

LOCATION:  New Jersey with partial work@home flexibility

Our client is situated within reasonable commuting distance of all areas in North and Central NJ, as well as Eastern Pennsylvania, Southern New York State, and New York City. This area of NJ is near many other pharmas (and Fortune 500 companies) as well as to New York City via public transportation, has a diverse international culture, has many top-ranked public school systems, and feature diverse places to live (small cities, suburbia, farm/horse country).

RELOCATION BENEFITS: Our client can provide relocation assistance.

ATTRACTIVE FEATURES ABOUT THIS POSITION AND COMPANY:

  • High Visibility: In this smaller environment, you’ll have direct and frequent interaction with the CMO and Heads of Reg Affairs, Drug Safety, etc. Their culture fosters collaboration and welcomes input. This environment allows someone to make a real impact on programs and in building this company’s infrastructure and SOPs, which is hard to achieve in slow-moving, multi-layered, and oft-politicized larger pharma.
  • Large & Diverse Pipeline: Our client’s self-discovered pipeline features multiple candidates in each stage (Phase I – III) and addresses a wide range of solid and liquid tumor indications.
  • Strong Funding: This public biotech has the necessary cash reserves to support the development of its large pipeline.
  • Share in the Company’s Success: This publicly traded company has an extremely attractive long-term incentive stock plan. With this company’s pipeline in a position to yield multiple products submissions over the next 1-2 years, this is an opportunity to share in the success of a company at a critical stage in its growth cycle.

RESPONSIBILITIES: CHALLENGES, EXPECTATIONS AND DELIVERABLES FOR THIS POSITION:

  • Work with senior level Clinical Development Leads and the CMO to direct and support the planning and implementation of clinical programs at all stages, with an initial focus on a Phase III global program.
  • Review, analyze and interpret study results, including exploratory endpoints, ensuring appropriate data review and accurate data reporting are completed.
  • Interpret safety and efficacy results data, including gathering, analyzing, reviewing, interpreting, and providing preliminary assessments and recommendations.
  • Contribute to database lock, statistical analysis plans, and the preparation of CSRs, IBs, INDs, NDAs (US, EU, Japan) and other regulatory submissions.
  • Provides support for advisory boards, consultant meetings, and investigator meetings, including preparation and/or delivery of presentations.
  • Partner with CPMs to ensure study execution is progressing per timelines, milestones, and expected deliverables.
  • Develop and maintain SOPs and working practices.

DESIRED SKILLS / EXPERIENCES / ACCOMPLISHMENTS / QUALITIES / EDUCATION:

  • PhD / PharmD / MD preferred
  • Ideally 5+ years of oncology clinical development experience that can be a mix of clinical research science along with clinical operations, medical writing, etc.
  • Phase III and NDA/BLA experience is a plus.
  • Leadership and influencing skills.
  • The demonstrated ability to anticipate, recognize and resolve problems/issues that may impact timelines and deliverables

CONTACT:

Thomas Fascia | Partner

E: tfascia@cornerstonesg.com | P: 973-656-0220 x717

LinkedIn: https://www.linkedin.com/in/thomasfascia

CORNERSTONE SEARCH GROUP - Life Sciences Executive Search

Six Campus Drive | Suite 301 | Parsippany, New Jersey 07054 USA

www.cornerstonesg.com | 973.656.0220

Prior Examples of Retained Search Assignments:

  • CEO | specialty start-up
  • US CEO | established European small pharma
  • CMO | late-stage public biotech
  • CMO | mid-size pharma
  • CSO | mid-size global biotech
  • President/US Commercial Head | OSD generics
  • SVP, Head of Global Medical Affairs | mid-size oncology company
  • SVP, Head of Global Regulatory Affairs | late-stage Israeli biotech
  • Group VP, Global Commercial Head | API Business Unit | Indian pharma
  • VP, Global Commercial Strategy – Early Pipeline | top rare disease biotech
  • VP, Global Head of Biometrics | NYC commercial-stage biotech
  • VP, Head of Regulatory Affairs | Boston biotech
  • VP, Head of Regulatory Affairs | NYC commercial-stage biotech
  • VP, Head of R&D Operations | Boston biotech
  • VP, Head of Health Economics & Outcomes Research | Top CNS specialty pharma
  • VP, Head of Real-World Evidence | Top 5 pharma
  • VP, Head of Heme/Onc Clinical Research | Public oncology biotech
  • Executive Director, Head of Global Clinical Pharmacology | Public oncology biotech
  • Executive Director, Head of US Drug Safety & PV | Chinese oncology biotech
  • Medical Director, Clinical Development | Boston biotech
  • Medical Director, Translational Medicine, Neuroscience | Top 5 Biotech

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Keywords: cancer CRS CRP New York Pennsylvania I-O immunooncology immuno-oncology

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