Clinical Data Analyst

Integrated Resources, Inc.Jersey City

On-site Full-time

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Experience Level

Entry Level

Qualifications

The ideal candidate will possess a strong background in data analysis, preferably within the healthcare sector. A Bachelor's degree in a relevant field such as Health Informatics, Statistics, or a related discipline is required. Proficiency in statistical software and data visualization tools is essential, along with excellent analytical skills and attention to detail.

About the job

We are seeking a detail-oriented Clinical Data Analyst to join our dynamic team. In this role, you will be responsible for analyzing clinical data to support healthcare research and improve patient outcomes. You will collaborate with clinical teams to ensure data integrity and compliance with regulatory standards, while also utilizing advanced analytical tools and methodologies.

About Integrated Resources, Inc.

Integrated Resources, Inc. is a leading provider of staffing solutions in the healthcare industry. With a commitment to excellence, we strive to connect talented professionals with innovative organizations. Our team is dedicated to fostering a culture of collaboration and integrity, ensuring that we meet the needs of both our clients and our employees.

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Clinical Data Analyst

Integrated Resources, Inc.

Full-time|On-site|Jersey City

We are seeking a detail-oriented Clinical Data Analyst to join our dynamic team. In this role, you will be responsible for analyzing clinical data to support healthcare research and improve patient outcomes. You will collaborate with clinical teams to ensure data integrity and compliance with regulatory standards, while also utilizing advanced analytical too…

Apr 30, 2015

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Clinical Data Analyst

Integrated Resources, Inc.

Full-time|On-site|Jersey City

Join our dynamic team as a Clinical Data Analyst at Integrated Resources, Inc., where you will play a pivotal role in transforming healthcare data into actionable insights. In this position, you will analyze clinical data, ensuring accuracy and compliance while supporting decision-making processes within our organization.

Mar 31, 2015

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Clinical Data Analyst

Integrated Resources Inc.

Full-time|On-site|Jersey City

Join Integrated Resources Inc. as a Clinical Data Analyst and play a pivotal role in our mission to improve healthcare outcomes through data-driven insights. You will analyze clinical data sets, ensuring accuracy and compliance while contributing to impactful research initiatives.

Mar 31, 2015

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Clinical Data Manager

Artech Information Systems LLC

Contract|On-site|Jersey City

We are seeking a detail-oriented and experienced Clinical Data Manager to join our dynamic team. In this role, you will be responsible for overseeing the collection, management, and analysis of clinical data to ensure accuracy and compliance with regulatory standards. Your expertise will support our mission in delivering high-quality clinical outcomes.

Aug 12, 2016

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dstaff

Full-time|On-site|Jersey City

Join dstaff as a Data Risk Reporting Business Analyst where you will play a pivotal role in enhancing our data risk management framework. You will collaborate with cross-functional teams to analyze data trends, identify risk factors, and contribute to the development of comprehensive reporting mechanisms. Your analytical skills will be essential in ensuring data integrity and compliance across various projects.

May 13, 2015

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Data Analyst at ConsultAdd Inc. | Jersey City

ConsultAdd Inc.

Full-time|On-site|Jersey City

Ensure the integrity and accuracy of metadata within the master and control files of our database environment.Regularly update master and control files as necessary to maintain data accuracy.Investigate, research, and analyze any data errors or inconsistencies that arise within the database system.Propose suitable corrective measures to resolve identified issues.Communicate effectively with database users to discuss problems and potential solutions.Generate and critically review various system reports to provide insights and support decision-making.Address requests for reports or specific information promptly and efficiently.Document all processes related to system files and reports to ensure clarity and compliance.Suggest improvements to the database or coordinate modifications with relevant personnel as required.Gain familiarity with operational and legacy data sources to enhance understanding of analytic data lineage and repositories.Engage in source-to-target data mapping to support data integration efforts.

Sep 1, 2015

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Lab Data Manager

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Full-time|$104K/yr - $114K/yr|Hybrid|Jersey City, NJ; Millbrae, CA

Eikon Therapeutics is a pioneering biopharmaceutical company that leverages cutting-edge technology at the crossroads of chemistry, engineering, computation, and biology to develop innovative therapies for life-threatening illnesses. Our discovery platform is founded on the groundbreaking work of our founders (Nobel Prize, 2014), leading to the development of advanced microscopy techniques that allow real-time, molecular-resolution tracking of protein dynamics in living cells, thereby revealing previously elusive drug targets.Position OverviewAs the Lab Data Manager, you will oversee the efficient and high-quality management of local lab reference ranges integral to the Eikon portfolio. This includes entering Lab Normal Ranges (LNR) into the EDC system and managing LNR issue tracking, as well as the health status of specific labs, sites, or studies.This role necessitates a minimum of three days of on-site work per week (or more as needed) at either our Jersey City, NJ office or our Millbrae, CA office, to ensure effective management and operational excellence in clinical studies while facilitating significant team expansion and collaboration.Your ProfileYou are a detail-oriented professional with a deep expertise in data management and a proven ability to collaborate effectively.Key ResponsibilitiesConduct thorough reviews and quality control (QC) of reference ranges submitted by sites or other relevant Eikon functional groups.Generate lab normal range import files and upload them into the EDC local lab module.

Feb 24, 2026

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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.

Aug 12, 2016

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Join Areté Technologies, Inc. as a Healthcare Business Analyst and play a pivotal role in enhancing healthcare solutions. In this position, you will analyze and interpret healthcare data, collaborate with cross-functional teams, and contribute to strategic initiatives that improve patient outcomes. Your analytical skills will be key in identifying trends and recommending actionable insights based on data-driven analysis.

Jun 5, 2017

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Clinical Trial Manager

Collabera

Full-time|On-site|Jersey City

We are seeking a dedicated and detail-oriented Clinical Trial Manager to join our dynamic team at Collabera. In this role, you will be responsible for overseeing the planning, execution, and management of clinical trials, ensuring compliance with regulatory requirements and adherence to study protocols.Your expertise will contribute to the successful delivery of clinical projects from initiation to completion, coordinating with cross-functional teams to meet timelines and objectives. The ideal candidate will possess excellent organizational skills and the ability to lead and motivate a team in a fast-paced environment.

May 18, 2016

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Clinical Trial Assistant

Collabera

Full-time|On-site|Jersey City

We are seeking a detail-oriented and motivated Clinical Trial Assistant to join our dynamic team. In this role, you will support clinical trial activities by ensuring compliance with regulatory requirements and assisting in the coordination of clinical research projects. Your responsibilities will include managing documentation, assisting with trial logistics, and collaborating with cross-functional teams to facilitate the successful execution of clinical trials.

May 4, 2016

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Clinical Program Manager in Oncology

Eikon Therapeutics

Full-time|On-site|Millbrae, CA; Jersey City, NJ

As a Clinical Program Manager specializing in Oncology at Eikon Therapeutics, you will play a pivotal role in coordinating and overseeing clinical programs that are crucial to advancing our innovative therapies. Your expertise will help align cross-functional teams, ensuring the successful execution of clinical trials and adherence to regulatory requirements.

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Clinical Trial Manager, Oncology - Asia

Eikon Therapeutics

Full-time|$130K/yr - $142.5K/yr|Hybrid|Jersey City, NJ; Millbrae, CA

Eikon Therapeutics is an innovative biopharmaceutical company that leverages cutting-edge technology at the intersection of chemistry, engineering, computation, and biology to develop groundbreaking treatments for severe diseases. Eikon's discovery platform is founded on remarkable innovations from its esteemed founders (Nobel Prize, 2014), leading to the development of advanced microscopes that provide real-time, molecular-resolution imaging of protein dynamics in living cells, thereby unlocking new classes of proteins as viable drug targets.Position OverviewWe are in search of a dynamic and experienced Clinical Trial Manager (CTM) to strengthen our oncology Clinical Operations team. This position necessitates an on-site commitment of at least three days a week at our offices in Millbrae, CA, or Jersey City, NJ, to facilitate effective global clinical trial management. The ideal candidate will excel in independent work, demonstrate strong leadership capabilities, and actively engage as a team member in a fast-paced environment. Your contribution will be critical in delivering high-quality clinical study management, ensuring adherence to regulatory standards, and aiding in the planning, execution, and successful completion of global clinical trials.Language ProficiencyThis role requires proficiency in Mandarin, Cantonese, Japanese, or Korean alongside strong English language skills (reading, writing, and speaking) to effectively interact with colleagues and stakeholders at all levels. About YouYou are a detail-oriented trial leader with global experience, known for your strong communication skills and collaborative nature. You are passionate about operational excellence and dedicated to enhancing patient care for serious illnesses.Your ResponsibilitiesLead the clinical trial management process from inception to completion while ensuring regulatory compliance.Collaborate with cross-functional teams to drive project milestones and timelines.Monitor and report on the progress of clinical trials, addressing any challenges and implementing effective solutions.

Feb 24, 2026

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About AvePoint: AvePoint is a global leader in data security, governance, and resilience, transcending traditional solutions to build a secure data foundation that empowers organizations to collaborate confidently. With over 25,000 customers worldwide, the AvePoint Confidence Platform ensures the preparation, security, and optimization of critical data across platforms like Microsoft, Google, Salesforce, and more. Our extensive global channel partner program comprises approximately 5,000 managed service providers, value-added resellers, and systems integrators, making our solutions accessible in over 100 cloud marketplaces. Discover more at www.avepoint.com. At AvePoint, we believe in investing in our people. Our culture, driven by agility, passion, and teamwork, empowers you to shape your career, make a meaningful impact, and take ownership of your future. Unleash your potential! About the Role: We are on the lookout for a Product Data Scientist to enhance our data analytics team, driving data-informed decision-making and fostering product-led growth for our B2B SaaS products. In this pivotal role, you will analyze product performance, explore customer behavior, and design experiments aimed at optimizing acquisition, adoption, retention, and growth. You will work with diverse datasets, including customer transactions, feedback, telemetry, and technographics, to reveal actionable insights that will inform our product strategy and elevate customer experiences. Key Responsibilities: Analyze Product Performance: Assess commercial performance metrics across various product lines, bundles, and features in distinct segments. Enhance product-led growth metrics, such as user activation rates, feature adoption, expansion revenue, and virality. Identify trends, opportunities, and risks affecting revenue and adoption. Customer Behavior Analysis: Utilize statistical and machine learning methodologies to model customer usage patterns, needs, and retention drivers. Segment customers by lifecycle stage (e.g., new, activated, power users, churn risk) to inform targeted in-product experiences.

Mar 4, 2026

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Join our dynamic team at Integrated Resources Inc. as a Business Analyst. In this role, you will play a crucial part in analyzing business processes and identifying areas for improvement. Your insights will help shape strategic decisions and drive efficiency across the organization. We are looking for a proactive individual who is passionate about data analysis and has a keen eye for detail. You will collaborate with cross-functional teams to gather requirements, document processes, and recommend solutions that align with our business objectives.

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Associate Director of Clinical Pharmacology

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Full-time|$183K/yr - $199.5K/yr|Hybrid|Jersey City, NJ

Eikon Therapeutics is a pioneering biopharmaceutical company that leverages innovative technology at the confluence of chemistry, engineering, computation, and biology to create groundbreaking treatments for life-threatening diseases. Our discovery platform is founded on transformative innovations from our Nobel Prize-winning founders (2014), leading to the development of advanced microscopes capable of real-time, molecular-resolution measurements of protein movement in living cells, thus revealing previously inaccessible classes of proteins as potential drug targets.PositionWe are excited to invite an accomplished and proactive Associate Director of Clinical Pharmacology to join our dynamic Clinical Research & Development team. This role will be pivotal in advancing Modeling and Simulation within the Clinical Pharmacology group. Responsibilities will encompass non-compartmental analysis (NCA), population pharmacokinetics/pharmacodynamics (PK/PD), disease progression modeling, statistical and physiologically-based PK (PBPK) modeling, allometric scaling, quantitative systems pharmacology (QSP), clinical trial simulations, literature meta-analysis, machine learning, and other cutting-edge quantitative techniques. The selected candidate will collaborate closely with Clinical Pharmacology Project Leads to utilize quantitative strategies to elucidate the relationship between drug exposure and therapeutic response, facilitating the selection and justification of first-in-human doses, recommended Phase II doses (RP2D), and labeled dosing during regulatory discussions. This position necessitates a minimum of three days a week onsite presence at our Jersey City, NJ location to ensure effective management, operational excellence, and the successful execution of clinical studies, fostering significant team growth and collaboration.

Mar 13, 2026

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Join the Eikon Clinical Talent Community

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On-site|On-site|Jersey City, NJ; New York City, NY; Millbrae, CA

Eikon Therapeutics is a pioneering biopharmaceutical company leveraging transformative technology at the nexus of chemistry, engineering, computation, and biology. Our mission is to unveil innovative therapies for life-threatening diseases. Our unique discovery platform is powered by groundbreaking advancements from our founders (Nobel Prize, 2014) and has led to the development of microscopes that facilitate real-time, molecular-resolution observations of protein dynamics within living cells, thereby revealing previously inaccessible protein classes as viable drug targets.Become a Part of Our Clinical Talent CommunityIf you are passionate about propelling clinical research and development forward but don’t see an immediate opening that aligns with your qualifications, we invite you to connect with us.By joining our Clinical Talent Community, you will have the chance to:Share your skills and interests with our Talent Acquisition team.Be considered for upcoming clinical roles as they arise.Stay engaged and updated about Eikon’s expansion and achievements.If you are eager to contribute to advancements in clinical discovery and development, we encourage you to join our community so we can stay connected as the right opportunity arises.

Feb 24, 2026

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