Clinical Study Director

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 wi…

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

Join Our Team as a Senior Study Manager!As a Senior Study Manager at US Tech Solutions, you will play a pivotal role in overseeing complex Phase I and extended Phase I/II oncology clinical trials. You will be responsible for managing all aspects of these clinical studies, ensuring strict adherence to Bayer's standards, Good Clinical Practices (GCP), and all applicable regulatory requirements.Your primary responsibilities will include:Leading and managing cross-functional teams throughout the study lifecycle, from initial concept through to the final Clinical Study Report (CSR).Overseeing all study-related activities and providing critical input to the Operational Sub-team to ensure accurate tracking of study execution.Developing and managing study budgets, timelines, and quality deliverables, while proactively addressing any budgetary concerns.Coordinating study start-up activities, including CRO selection, CRF development, and recruitment planning.Collaborating with team members to write protocols and amendments, ensuring feasibility and site selection meet enrollment timelines.Your mission is to drive the planning, implementation, analysis, and reporting of clinical pharmacology studies, all while ensuring high-quality data and meeting global regulatory approval criteria. We are looking for someone who is proactive and seeks opportunities for global process improvement.

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 serious diseases. Our discovery platform is based on pioneering breakthroughs from our founders, including the Nobel Prize in 2014, resulting in the development of advanced microscopes that enable real-time, molecular-resolution tracking of protein dynamics within living cells, thus opening new avenues for drug target discovery.Position OverviewWe are on the lookout for an accomplished physician with a solid clinical background and a fervor for drug development to join our Clinical Development team as the Senior Director of Clinical Research. In this crucial role, you will significantly impact the progression of our oncology and/or non-oncology pipeline by providing expert medical input, leadership, and operational oversight for clinical studies.Your ProfileYou are a distinguished professional excelling in the execution and advancement of clinical projects. As a vital member of our cross-functional Development and Clinical Study Teams, you will leverage your clinical development expertise to bring new therapies to patients in need. Your commitment to scientific integrity and meticulous attention to detail is reflected in your work, driven by a passion for creating impactful new medicines and enhancing patient outcomes.This position mandates a minimum of three days per week of onsite engagement (or more as business needs dictate) at our New Jersey offices to foster effective collaboration and ensure high-quality execution of your clinical responsibilities.

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.

$90,000–$120,000 + Signing Bonus + Leadership Growth PathAccelerate Your Career. Step into Leadership. Transform Lives.Join SportsMed Physical Therapy as we expand our team of Staff Physical Therapists and Clinic Directors throughout New Jersey.Whether you are a recent graduate seeking comprehensive mentorship or an experienced professional ready to embrace a leadership role, we offer a well-defined growth trajectory.We don’t just provide jobs; we cultivate careers.

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.

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.

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.

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.

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.

Join AbbVie, a global biopharmaceutical company, as a Senior Medical Director in our Late Stage Oncology division. In this pivotal role, you will lead the strategic direction and execution of clinical development programs aimed at advancing innovative cancer therapies. Collaborate with cross-functional teams to drive clinical trial design, oversee regulatory submissions, and contribute to the overall vision of oncology research.

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.

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.

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.

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.

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.

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.

We are seeking a dedicated and detail-oriented Clinical Supply Manager to join our dynamic team at Integrated Resources, Inc. In this role, you will oversee the management of clinical supplies for various projects, ensuring timely delivery, compliance with regulations, and effective communication with stakeholders.

Role overview The Associate Director / Director - Client Partner at Tiger Analytics plays a central role in building and sustaining trusted relationships with clients in Jersey City, New Jersey. This leadership position involves direct engagement with clients and active participation in shaping analytical solutions that address business needs. The role requires a balance of strategic vision and hands-on involvement in project delivery. Key responsibilities Lead client engagements and manage ongoing relationships with key stakeholders. Oversee the delivery of analytical solutions to ensure they align with client objectives. Drive strategic initiatives that produce measurable results for clients. Work closely with internal teams to turn client challenges into actionable, data-driven solutions. Requirements Experience managing client partnerships, preferably within analytics or data-focused consulting. Proven leadership skills with the ability to influence both clients and internal teams. Comfort tackling complex business problems and developing practical solutions. Interest in applying data and analytics to address real-world business challenges.