Remote Jobs at Eikon Therapeutics

Candidates should possess a postgraduate degree with over 10 years of experience or a bachelor's degree with over 12 years of experience in computer system validation and quality assurance within the biotech or pharmaceutical industry. In-depth knowledge of regulatory requirements such as FDA and GxP pertaining to computer system validation and quality assurance is essential, along with proficiency in writing validation documentation and strong analytical, problem-solving, leadership, and commun…

Candidates must possess a minimum of 10 years of related experience with a Bachelor's degree, or 8 years with a post-graduate degree. Experience leading large, global clinical trials, preferably in oncology, is essential, along with in-depth knowledge of ICH-GCP guidelines. A minimum of 3 days per week onsite presence in California or New Jersey offices is required.

- Seasoned regulatory professional with in-depth knowledge of ex-US regulatory requirements and guidelines (e.g., EU-CTR Regulation EU No 536/2014, ICH, country-specific regulations) - Exceptional project management, coordinating, and communication skills - Proven ability to thrive in a fluid, fast-paced, collaborative, cross-functional team environment - Strong analytical skills, attention to detail, effective problem-solving abilities, efficient execution, and adaptability - Minimum of 3 days …

- Passion for advancing clinical research and development - Relevant experience and interests in clinical roles

- Task-driven and process-oriented individual dedicated to delivering project success by ensuring quality, compliance, and timeliness of TMF documents - Strong communication skills to work well as part of a team and independently - Detail-oriented with ability to escalate non-compliance or quality issues to stakeholders in a timely manner - Minimum of 3 days a week onsite presence in Jersey City (NJ) or Millbrae (CA) offices (or more as business needs require) - Knowledge of applicable Standard …

- Minimum of 4-6 years of related experience - Works on assignments requiring considerable judgment and initiative - Understands implications of work and makes recommendations for solutions - Experience with performing maintenance tasks and qualification checks on integrated automation systems - Available to work Tuesday-Saturday (swing shift: 2:30pm – 11:00pm) - Experience with support ticketing systems (Jira is preferred) - Experience maintaining parts inventory through CMMS (Computerized Main…

- Post Graduate degree with 6+ years of experience or a Bachelor's degree with 8+ years of experience in a relevant scientific discipline - Strong knowledge of FDA and international regulatory requirements and guidelines - Excellent communication, negotiation, and project management skills - Ability to work effectively in a cross-functional team environment - Attention to detail, strong analytical skills, and problem-solving abilities - Adaptable and able to thrive in a fast-paced, high-growth e…

- Bachelor’s degree in chemistry and a minimum of 2 years relevant EHS experience working with chemical waste, handling hazardous materials, or working as a generalist member in an EHS organization - Experience working in a regulated environment such as biopharma, medical device, clinical lab, diagnostics, vaccines - Knowledge of California and Federal regulations related to chemicals, biological materials, power tools/machine, lasers, injury prevention, emergency response - Familiarity with haz…

- Bachelor’s degree in Neuroscience, Stem Cell Biology, or a related field with a minimum of 6+ years of academic and/or industry experience; or Master’s degree with 4+ years of relevant experience - Extensive experience in cell culture techniques, including primary neuronal cultures, iPSC maintenance, and neuronal differentiation - Proficiency in molecular biology and biochemical assays, such as Western analysis, qRT-PCR, IPs, and ELISAs - Excellent interpersonal and communication skills with a…

- Thrive on solving complex problems - Experience building innovative technologies - Interest in enabling science through engineering - Expertise in software, hardware, data, or platform engineering - Excitement about applying engineering to transform biopharma and accelerate innovation

- Background in legal, finance, HR, IT, or IS (G&A functions) - Passion for enabling scientific and clinical innovation through strong business, legal, and operational foundations - Excitement about contributing expertise to scale and strengthen a growing biopharma company

- MD degree - Minimum of 7+ years of experience in pharmacovigilance or drug safety - Strong understanding of pharmacovigilance regulations and processes - Exceptional leadership and team management skills - Strong organizational and communication skills - Meticulous attention to detail and analytical abilities - Proficiency in pharmacovigilance tools and software - Ability to collaborate with cross-functional teams - Minimum of 3 days a week onsite presence in New Jersey office (or more as busi…

- Bachelor’s degree with 5+ years of experience, or Master’s degree with 3+ years of experience in clinical research, clinical finance, or site payments - Strong understanding of site contract terms and clinical trial operations - Excellent analytical, organizational, and communication skills with high attention to detail - Proven ability to work independently and exercise sound judgment in a dynamic, fast-paced environment - Demonstrated ability to build relationships, adapt communication to di…

- Bachelor's degree with 15 years of relevant experience or a master's degree with 12 years of relevant experience or a PhD with 8 years of relevant experience in Computer Science, Software Engineering or a related field - Strong proficiency in React, TypeScript, Postgres and Python - Experience in multiple strongly typed languages such as C++, C# or Java - Successful track record designing software and systems architecture, including API and database design, commercial application development, …

- PhD or equivalent degree in statistics/biostatistics or related discipline with a minimum of 6 years of clinical research and drug development experience - Proficiency in statistical programming languages (e.g., R, SAS) and experience with data visualization tools - Strong understanding of regulatory guidelines (ICH, FDA, etc.) and their implications on statistical analysis and reporting - Experience in authoring statistical analysis plans and performing statistical analyses and reporting usin…