New

Vice President Clinical Research & Development, Oncology

Jersey City, NJ

Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.

Position

Clinical Development at Eikon Therapeutics is seeking a physician-scientist to serve as a Study Responsible Physician and Project Lead for novel Oncology compound(s) across all stages of development, from First-in-Human/Phase 1 until proof-of-concept through phase 3. In this role, you will reside within Clinical Development reporting to the Head of Oncology Clinical Development.

About You

You are a highly accomplished professional who excels in leading the development and execution of clinical projects. You will be responsible for the development and execution of clinical projects as a leader of the cross-functional Development Team and as the co-leader of the Clinical Study Team. You will employ your expertise in clinical development to advance new therapies to patients in need. Your dedication to scientific rigor and meticulous attention to detail is evident in all your work. With a deep passion for creating important new medicines, you are committed to advancing the field of medical research and improving patient outcomes. This role will require a minimum of 3 day a week of onsite presence (or more as business needs require) in our New Jersey office to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration. 

What You’ll Do

  • Design and conduct early clinical Phase 1, proof-of-concept development and late-stage trials, assess clinical safety and efficacy data, and write clinical study reports, clinical sections of INDs, investigator brochures, etc.
  • Work closely with biomarker, discovery, and translational research scientists.
  • Interpret reports, prepare oral and written results of product research, and participate in the discussion of strategies formulated within the disease areas that Eikon is focusing on.
  • This role requires a knowledge of clinical and translational research involving biomarkers and correlative laboratory clinical trial endpoints.
  • As program needs grow, recruit, lead and mentor a team of empowered and motivated clinical development staff, driving a compelling vision and aligning the team to achieve success in developing the program assets.
  • Collaborate closely with relevant functions within Eikon and potential partners including discovery, translational, and biomarker research scientists, toxicologists, clinical pharmacologists, drug safety specialists, regulatory representatives, as well as personnel from Clinical Science and Global Clinical Operations, and other support functions.
  • Establish strong working relationships and collaborations with external study investigators, key opinion leaders in drug development, and external alliance partners.
  • Work closely with functional partners (Data Management, Biostatistics, Regulatory, GCO) to ensure an integrated and strategic approach to flawless execution and systematic oversight of study protocol(s) in early development in close collaboration with key functional stakeholders.
  • Working in partnership with colleague study responsible physicians and clinical scientists to ensure development of high-quality study protocols including use of consistent processes/standards across studies.
  • Work closely with functional partners to address protocol questions from Health Authorities and Ethics Committees in a consistent fashion.

Qualifications

  • M.D. with 16+ years of experience in clinical research within a relevant field, such as the pharmaceutical industry, biotechnology, or academia.
  • Demonstrated experience in both line management and matrixed team leadership.
  • Knowledge of translational and clinical cancer research and its application to cancer drug development.
  • In-depth knowledge of clinical research methodologies, GCP, and regulatory requirements.
  • Ability to lead effectively in a matrixed environment.
  • Strong analytical, organizational, and problem-solving skills.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners.
  • Passion for innovation and improving patient outcomes.
  • Experience with IND and/or NDA filings is strongly preferred.
  • Oncology experience with board certification or eligibility is preferred.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

  • 401k plan with company matching​
  • Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
  • Mental health and wellness benefits​
  • Weeklong summer and winter holiday shutdowns​
  • Generous paid time off and holiday policies​
  • Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
  • Enhanced parental leave benefit​
  • Daily subsidized lunch program when on-site​

The expected salary range for this role is $348,000 to $380,000 depending on skills, competency, and the market demand for your expertise.

Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.

We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.

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