Clinical Study Director

Artech Information Systems LLCJersey City

On-site Full-time

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Experience Level

Senior Level Manager

Qualifications

Proven experience in clinical study management. Strong understanding of regulatory requirements and Good Clinical Practice (GCP). Excellent leadership and communication skills. Ability to collaborate effectively with diverse teams and stakeholders. Advanced degree in life sciences or related field preferred.

About the job

Join our dynamic team as a Clinical Study Director, where you will play a pivotal role in leading clinical studies that contribute to advancing healthcare solutions. In this strategic position, you will oversee the planning, execution, and management of clinical trials, ensuring compliance with regulatory standards and organizational goals. Your expertise will guide cross-functional teams and drive innovative solutions in clinical research.

About Artech Information Systems LLC

Artech Information Systems LLC is a leading provider of workforce solutions and staffing services. We specialize in connecting top-tier talent with organizations in various sectors, including healthcare, technology, and finance. Our commitment to excellence and innovation makes us a trusted partner in the industry.

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Flywheel Digital supports major brands as they grow across digital marketplaces. The company’s platform provides clients with near real-time performance data to help improve sales, market share, and profitability. Teams operate in the Americas, Europe, and APAC. Role overview The Associate Director of Platform Solutions (Contract) leads key initiatives for s…

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Associate Director of Client Services - Learning & Development (Contract)

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Director of Clinical Study Management (Contract)

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Contract|On-site|Millbrae, CA; Jersey City, NJ

Role Overview The Director of Clinical Study Management (Contract) at eikontherapeutics leads the planning and execution of clinical studies. This position oversees the clinical study team and ensures studies follow regulatory guidelines, stay on schedule, and remain within budget. Location Millbrae, CA or Jersey City, NJ

Apr 14, 2026

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Associate Director of Biostatistics

Eikon Therapeutics

Full-time|$200K/yr - $218.5K/yr|Hybrid|Jersey City, NJ

Eikon Therapeutics is an innovative biopharmaceutical company harnessing cutting-edge technology at the crossroads of chemistry, engineering, computation, and biology to develop groundbreaking treatments for critical health conditions. Our discovery platform is founded on transformative innovations from our Nobel Prize-winning founders (2014), leading to the development of advanced microscopes that facilitate real-time, molecular-resolution observations of protein dynamics in living cells. This approach opens new avenues in targeting previously untouchable classes of proteins for drug development.Position OverviewWe are on the lookout for a talented and driven Associate Director of Biostatistics to enhance our dynamic team. The successful candidate will leverage their statistical knowledge and strategic acumen to oversee the design, implementation, and analysis of clinical trials and experimental studies. Working in close collaboration with cross-functional teams, you will spearhead statistical initiatives that underpin data-driven conclusions and inform our research and development strategies.This position necessitates a minimum of three days per week on-site presence in our New Jersey office to ensure effective leadership, operational excellence, and high-quality execution of clinical studies while supporting the anticipated significant team growth and collaboration.Your ProfileThe ideal candidate will have a proven history of designing and analyzing clinical trials and experimental research, particularly within the biotechnology, pharmaceutical, or allied sectors. This individual excels in leading interdisciplinary teams to formulate study designs, develop statistical analysis plans, perform advanced statistical evaluations, and mentor team members. Expertise in statistical programming languages, a thorough understanding of regulatory requirements, and outstanding communication skills are crucial for articulating complex statistical concepts to non-technical audiences. The perfect candidate will also demonstrate strong leadership skills and a comprehensive understanding of the latest trends and best practices in biostatistics, statistical tools, and software.

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Associate Director of Biostatistics

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Full-time|$200K/yr - $218.5K/yr|Hybrid|Jersey City, NJ

Eikon Therapeutics develops new treatments for life-threatening diseases by combining chemistry, engineering, computation, and biology. The company’s discovery platform draws on innovations from its founders, including a 2014 Nobel Prize winner, and features advanced microscopes that measure protein dynamics in living cells at molecular resolution. This technology enables drug discovery for protein classes that were previously out of reach. Role Overview The Associate Director of Biostatistics will guide statistical strategy and execution for clinical trials and experimental studies. This leader will work closely with cross-functional teams to design studies, implement statistical methods, and interpret results that support research and development. The role is based in Jersey City, NJ, and requires at least three days per week on site, with flexibility to increase as business needs grow and the team expands. What You Will Do Design and analyze clinical trials and experimental studies Lead interdisciplinary teams in study design and statistical planning Develop and review statistical analysis plans Conduct advanced statistical analyses Mentor and support team members in statistical methods and best practices Collaborate with other departments to ensure statistical rigor in research What We Look For Experience designing and analyzing clinical trials or experimental studies in biotechnology, pharmaceuticals, or related fields Strong leadership skills and experience guiding interdisciplinary teams Proficiency in statistical programming languages Knowledge of regulatory standards relevant to clinical research Clear communication skills, especially when explaining statistical concepts to non-technical colleagues Awareness of current trends, tools, and best practices in biostatistics Location and On-Site Requirement This position is based in Jersey City, NJ. A minimum of three days per week on site is required, with flexibility to adjust as team and business needs evolve.

Apr 16, 2026

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Full-time|On-site|Jersey City

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Clinical Study Director

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Full-time|On-site|Jersey City

Join our dynamic team as a Clinical Study Director, where you will play a pivotal role in leading clinical studies that contribute to advancing healthcare solutions. In this strategic position, you will oversee the planning, execution, and management of clinical trials, ensuring compliance with regulatory standards and organizational goals. Your expertise will guide cross-functional teams and drive innovative solutions in clinical research.

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