Associate Director, Clinical Scientist at Eikon Therapeutics

Millbrae, California, United States

Eikon Therapeutics Logo
Not SpecifiedCompensation
Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Biopharmaceutical, BiotechnologyIndustries

Requirements

  • 10+ years of experience with a Bachelor's degree, or 8+ years with a post graduate degree
  • Experience in clinical drug development, or a PhD, Pharm D, or RN degree is preferred
  • Solid knowledge of clinical research regulatory requirements (e.g., GCP and ICH)
  • Ability to manage multiple competing priorities with good planning, time management and prioritization skills
  • Strong analytical skills with the ability to interpret clinical trial data and synthesize conclusions
  • Proficient scientific expertise to propose, design, and execute clinical research and development studies
  • Minimum of 3 days a week onsite presence in Jersey City (NJ) or Millbrae (CA) offices (or more as business needs require)

Responsibilities

  • Lead specific aspects of clinical/scientific execution of clinical protocol(s)
  • Serve as the lead clinical scientist on the clinical trial team
  • Lead medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaboration with Clinical Research and Pharmacovigilance
  • Collaborate cross-functionally in the development of Protocol and related study materials (e.g., ICF documents/amendments); partner with Clinical Operations on study deliverables
  • Ensure CRF design supports data collection in alignment with the Protocol in collaboration with Clinical Data Management/Programming
  • Collaborate cross-functionally to monitor clinical data to ensure quality, completeness, and integrity of trial conduct
  • Provide tactical/scientific mentorship to other clinical scientists
  • Assist with the generation, analysis, and presentation of clinical data, including manuscripts, abstracts, and oral presentations (including authoring documents and slide preparation as appropriate)
  • Apply proficient analytical knowledge and skills to understand how program objectives and design impact data analysis; identify risks and design mitigation strategies
  • Promote consistent first line medical/clinical data review techniques and conventions across studies/programs

Skills

Key technologies and capabilities for this role

Clinical TrialsProtocol DevelopmentData AnalysisPharmacovigilanceClinical OperationsStudy ImplementationRegulatory ApprovalScientific WritingCross-Functional CollaborationElectronic Data Capture

Questions & Answers

Common questions about this position

Is this role remote or does it require office presence?

The role requires a minimum of 3 days a week of onsite presence (or more as business needs require) in either Jersey City (NJ) or Millbrae (CA) offices.

What are the key responsibilities of this Clinical Scientist role?

Responsibilities include leading aspects of clinical/scientific execution of protocols, serving as lead clinical scientist on trial teams, leading medical monitoring, collaborating on protocol development and study materials, ensuring CRF design aligns with protocols, monitoring clinical data quality, and providing mentorship to other scientists.

What skills and qualities are they looking for in candidates?

They seek a data-driven and collaborative integrator passionate about therapeutic strategy, with exemplary communication and presentation skills, and the ability to lead study development using current electronic document conventions to ensure scientific and data integrity.

What is the salary or compensation for this position?

This information is not specified in the job description.

What kind of team and work environment can I expect?

The role involves working as part of a cross-functional clinical development team with collaboration across Clinical Research, Pharmacovigilance, Clinical Operations, and others, supporting significant team growth in an environment focused on high-performance delivery of clinical studies.

Eikon Therapeutics

Biotech startup developing innovative medicines

About Eikon Therapeutics

Eikon Therapeutics focuses on discovering and developing new medicines in the pharmaceutical industry. The company employs advanced technologies to study biological systems, aiming to identify new drug targets by examining the dynamic aspects of biology rather than just static chemical processes. Their team consists of diverse professionals, including data scientists, chemists, and engineers, which allows them to combine science and engineering to create new therapies that aim to improve and extend life. A key feature of Eikon's approach is their proprietary single-molecule tracking (SMT) platform, which enables rapid visualization of protein movements in living cells. This technology, along with artificial intelligence and automation, allows for precise inventorying of molecular interactions. Eikon Therapeutics targets patients with serious diseases who need effective treatments, generating revenue through the development and commercialization of their therapies.

Hayward, CaliforniaHeadquarters
2019Year Founded
$750.8MTotal Funding
SERIES_CCompany Stage
AI & Machine Learning, BiotechnologyIndustries
201-500Employees

Benefits

401(k) Company Match
Medical (premiums covered by Eikon at 95%)
Dental Insurance
Vision Insurance
Mental Health Support
Unlimited Paid Time Off
Paid Holidays
Life Insurance
Enhanced Parental Leave
Daily subsidized lunch program

Risks

Competition from biotech unicorns like Abogen Biosciences is increasing.
Integrating new clinical-stage assets may delay drug development timelines.
Reliance on SMT technology risks obsolescence from emerging molecular biology technologies.

Differentiation

Eikon uses proprietary single-molecule tracking for real-time protein movement analysis.
The company integrates AI and automation for large-scale molecular interaction studies.
Eikon's diverse team combines expertise in science, engineering, and technology.

Upsides

Growing interest in SMT technology boosts Eikon's drug discovery potential.
Partnerships with AI firms enhance Eikon's drug candidate identification.
Rising demand for precision medicine aligns with Eikon's focus on dynamic biology.

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