Jobs at Cryo Beauty Hub

This five-month contract role serves as a Patient Recruitment Specialist supporting clinical trial operations at a Princeton, New Jersey facility with hybrid onsite requirements. The position focuses on designing and executing scalable, patient-centered recruitment strategies to accelerate enrollment and improve diversity across global studies. Key responsibilities include developing protocol-specific tactics through partnerships with advocacy groups and digital platforms, analyzing performance metrics to refine engagement approaches, and collaborating with cross-functional teams to align recruitment efforts with scientific priorities. The role appeals to candidates seeking to drive meaningful impact in inclusive clinical research within a collaborative, innovation-focused environment that values data-driven decision-making and strategic stakeholder management.

The OnCore Training Specialist role within the Clinical Research Support Office focuses on supporting the OnCore Clinical Trials Management System across the university campus. Key responsibilities include serving as a subject matter expert to provide technical support and workflow optimization, designing and delivering comprehensive training programs for end-users, and collaborating with leadership to assess evolving educational needs. The position appeals to candidates interested in clinical research by offering a collaborative environment with opportunities for professional growth and access to comprehensive employee benefits. The role is full-time and requires the incumbent to be available to work from the state of Utah.

This full-time Senior Clinical Research Associate role at Mobius serves as a primary site manager for a diverse portfolio of clinical trials across the USA, Australia, and New Zealand. The position focuses on overseeing the entire trial lifecycle, from study start-up and monitoring to data management and close-out, while ensuring strict adherence to FDA regulations and GCP standards. Key responsibilities include building strong relationships with investigators, troubleshooting compliance issues, mentoring colleagues, and managing project reporting to sponsors. The role appeals to experienced professionals seeking a collaborative environment where they can make a significant impact on bringing new therapies to patients. It offers remote flexibility for candidates in the Midwest, West, and Northeast, with travel required approximately one to two times per week to support US-based projects.

The Research Associate, Formulations role supports the discovery and development of new drug therapies within a collaborative CRO environment. Key responsibilities include preparing dose formulations, managing sample receipt and disposition, maintaining a clean GLP-compliant laboratory, and collecting accurate data according to study protocols. The position appeals to candidates seeking to make a meaningful impact on global health while working in a values-driven culture that prioritizes employee development and integrity. The company offers a comprehensive benefits package including health insurance, retirement matching, and professional training programs. While the role is primarily on-site, telework opportunities are available when applicable.

This full-time Clinical Laboratory Study Manager role supports the Precision Medicine Strategy Lead and cross-functional clinical teams to ensure high-quality sample and data delivery for biomarker evaluations. Key responsibilities include overseeing the entire lifecycle of clinical sample collection, processing, storage, and destruction while managing relationships with central laboratories and specialty vendors. The position also involves developing informed consent forms, coordinating data acquisition specifications, and ensuring strict compliance with study protocols and regulatory requirements. This opportunity appeals to professionals seeking a dynamic environment where they can drive scientific translation through robust project management and operational oversight. The role offers remote work flexibility and the chance to collaborate with diverse internal and external stakeholders in a mission-driven biotech setting.

This full-time QC Scientist role supports the launch of a new raw materials testing facility within Eurofins PSS in Gaithersburg, Maryland. The position focuses on performing analytical testing using techniques such as HPLC, GC, and FTIR in compliance with cGMP guidelines. Key responsibilities include executing wet chemistry and spectroscopic analyses, documenting results accurately, troubleshooting instruments, and managing minor deviations or change controls. The role offers a unique opportunity to grow within a supportive start-up lab environment while working with a global leader in life sciences. The company emphasizes professional development, work-life balance, and a collaborative culture. This on-site position requires candidates to be based near Gaithersburg and involves standard business hours.

The Clinical Laboratory Study Manager role supports the Precision Medicine Strategy Lead and cross-functional clinical teams to ensure high-quality sample and data delivery for biomarker evaluations. Key responsibilities include overseeing the full lifecycle of clinical sample collection, tracking, and storage, managing relationships with central and specialty laboratory vendors, and ensuring compliance with informed consent forms and study protocols. The position also involves coordinating data acquisition specifications and providing guidance to sites on sample handling procedures. This opportunity appeals to professionals seeking a remote position within a collaborative environment focused on translating scientific research into medicine. The role offers significant growth potential for individuals with six to eight years of experience in clinical research lab management who excel at problem-solving and project coordination.

This full-time Clinical Laboratory Study Manager role supports the Precision Medicine Strategy Lead and cross-functional teams to ensure high-quality sample and data delivery for clinical trials. Key responsibilities include overseeing the end-to-end management of human samples, including collection, processing, storage, and shipping, while ensuring strict compliance with study protocols and informed consent forms. The position also involves coordinating with data management leads for sample data acquisition, forecasting operational costs, and resolving complex sample-related issues with clinical sites and CROs. The role appeals to professionals seeking a remote opportunity within a collaborative environment that values scientific translation and operational excellence. It offers the chance to work independently on strategic projects while contributing to a mission of advancing medicine through robust biomarker evaluation.

The Clinical Laboratory Study Manager role supports the Precision Medicine Strategy Lead and cross-functional teams to ensure high-quality sample and data delivery for biomarker evaluations. Key responsibilities include overseeing the entire lifecycle of clinical sample collection, tracking, and destruction, while managing relationships with central laboratories and specialty vendors. The position requires coordinating with project managers to resolve sample-related issues, ensuring compliance with informed consent forms and study protocols, and facilitating accurate data transfer. This opportunity appeals to professionals seeking a remote position within a collaborative environment that values scientific translation and operational excellence. The role offers significant growth potential for individuals with extensive clinical research lab experience who excel at independent problem-solving and cross-team communication.

This Project Manager I role supports a sponsor-dedicated team within Syneos Health's Clinical Solutions division, focusing on high-impact oncology and cell and gene therapy trials including CAR-T studies. The position involves leading early-phase trial execution from startup through closeout, coordinating cross-functional stakeholders to meet timelines and budgets, and ensuring regulatory compliance and inspection readiness. While the role is primarily remote, it strongly prefers candidates located near the Los Angeles area to facilitate periodic in-person collaboration. The position is appealing for its unique blend of strategic sponsor-side engagement with CRO resources, offering opportunities to advance life-saving research and grow professionally within a mission-driven culture dedicated to accelerating patient progress.

The Associate Director of Global Marketing for Biologics Testing leads the strategic vision and execution for a specialized unit within Charles River's corporate functions. This role focuses on driving global marketing strategies for biologics testing solutions, including vaccines and advanced therapies, to support the discovery and development of new drug therapies. Key responsibilities include designing integrated marketing campaigns, analyzing performance metrics to optimize ROI, and collaborating with cross-functional teams to accelerate pipeline velocity. The position offers the appeal of working for a mission-driven organization with a 75-year history of improving global health, providing opportunities for significant career growth in a dynamic, remote-friendly environment with up to 30% travel.

This Principal Security Solutions Architect role within AWS Financial Services focuses on guiding major financial institutions through secure cloud adoption. The position involves addressing complex security, risk, and compliance challenges for C-level stakeholders while designing controls and automated assurance frameworks. Key responsibilities include leading architecture discussions to mitigate risk, educating auditors on third-party assessments, and developing technical content like white papers to support secure deployments. The role appeals to professionals seeking to influence industry standards through executive-level relationship building and mentorship. It offers a collaborative culture that values diverse experiences, continuous learning, and work-life balance, with opportunities for significant career growth within a global team.

The Clinical Laboratory Study Manager role supports the Precision Medicine Strategy Lead and cross-functional clinical teams to ensure high-quality sample and data delivery for biomarker evaluations. Key responsibilities include overseeing the entire lifecycle of clinical sample collection, tracking, storage, and destruction while managing relationships with central laboratories and specialty vendors. The position requires coordinating with data management leads to establish secure data transfer protocols and providing guidance to sites on compliance with informed consent forms and study protocols. This opportunity appeals to professionals seeking a remote position within a collaborative environment focused on translating scientific research into medicine. The role offers the chance to lead complex project management activities, drive operational efficiency, and contribute to the advancement of precision medicine initiatives.

This full-time Clinical Laboratory Study Manager role operates within the Precision Medicine Strategy team to support biomarker and non-biomarker evaluations. The position involves coordinating with clinical study teams, data management groups, and external vendors to ensure high-quality sample collection, processing, and data delivery. Key responsibilities include overseeing the entire sample lifecycle from collection to storage and shipping, managing operational budgets and timelines, and ensuring strict compliance with study protocols and informed consent forms. The role appeals to professionals seeking a dynamic environment where they can apply extensive clinical research experience to translate scientific findings into medicine. It offers remote flexibility and the opportunity to work collaboratively across multiple internal and external stakeholders in a mission-driven organization.

The Clinical Laboratory Study Manager role supports the Precision Medicine Strategy Lead and cross-functional clinical teams to ensure high-quality sample and data delivery for biomarker evaluation. Key responsibilities include overseeing the entire lifecycle of clinical sample collection, processing, storage, and destruction while managing relationships with central and specialty laboratory vendors. The position requires coordinating with data management groups to establish secure data transfer protocols and providing guidance to clinical sites on compliance with informed consent forms and study protocols. This opportunity appeals to professionals seeking a remote position within a collaborative environment focused on translating scientific research into medicine. The role offers significant growth potential for individuals with six to eight years of experience in clinical research lab management who excel at problem-solving and project coordination.

This full-time Clinical Laboratory Study Manager role operates within the Precision Medicine Strategy team to support biomarker and non-biomarker evaluations. The position involves coordinating with clinical study, data management, and logistics groups to ensure high-quality sample and data delivery. Key responsibilities include overseeing the entire lifecycle of human sample collection, processing, storage, and shipping while ensuring strict compliance with study protocols and informed consent forms. The manager also collaborates with data leads to define data capture methods and manages vendor relationships to align operational costs with budget plans. This opportunity appeals to professionals seeking a remote position within a collaborative environment that values scientific translation. The role offers the chance to work independently on complex clinical trial operations while contributing to a mission-driven organization focused on advancing medicine.

This full-time Clinical Laboratory Study Manager role supports the Precision Medicine Strategy Lead and cross-functional teams to ensure high-quality sample and data delivery for clinical trials. Key responsibilities include overseeing the end-to-end management of human samples, including collection, processing, storage, and shipping, while ensuring strict compliance with study protocols and informed consent forms. The position also involves coordinating with data management leads for sample data acquisition, forecasting operational costs, and resolving complex sample-related issues with clinical sites and vendors. This opportunity appeals to professionals seeking a remote position within a collaborative environment that values scientific translation and operational excellence. The role offers the chance to work independently on strategic projects while contributing to a mission-driven team focused on advancing medicine through biomarker evaluation.

This full-time Clinical Laboratory Study Manager role operates within the Precision Medicine Strategy team to support biomarker and non-biomarker evaluations. The position involves coordinating with clinical study teams, data management groups, and external vendors to ensure high-quality sample collection, processing, and data delivery. Key responsibilities include overseeing the end-to-end sample lifecycle from collection to storage, managing operational budgets and timelines, and guiding clinical sites on compliance with study protocols and informed consent forms. The role appeals to professionals seeking a dynamic environment where they can leverage six to eight years of clinical research experience to bridge the gap between laboratory science and clinical trial execution. The position offers remote flexibility and emphasizes a collaborative culture focused on translating scientific discoveries into medical advancements.

This full-time Clinical Laboratory Study Manager role supports the Precision Medicine Strategy Lead and cross-functional clinical teams to ensure high-quality sample and data delivery for biomarker evaluations. Key responsibilities include overseeing the entire lifecycle of clinical sample collection, processing, storage, and destruction while managing relationships with central and specialty laboratory vendors. The position requires coordinating with data management teams to establish secure data transfer protocols and providing guidance to clinical sites on compliance with informed consent forms and study protocols. This opportunity appeals to professionals seeking a remote position within a collaborative environment that values scientific translation and offers significant growth through involvement in complex clinical trial operations.

This senior biostatistician role supports statistical activities for clinical trials within a global research environment. Key responsibilities include contributing to trial designs, authoring statistical sections of protocols, preparing statistical analysis plans, and interpreting clinical trial data. The position requires managing contract research organization teams and facilitating interactions with cross-functional study groups and health authorities worldwide. The role offers the opportunity to work on high-impact studies with a focus on global regulatory engagement and collaborative team dynamics.

This full-time In Vivo Research Associate role is based on-site in Boston, MA, within Eurofins Scientific's biopharmaceutical testing division. The position focuses on executing rodent experiments to evaluate pharmacokinetics, ADME properties, and mechanisms of action for new therapeutics. Key responsibilities include designing and performing in-life procedures such as drug administration, sample collection, and necropsy, as well as collaborating with the team to troubleshoot novel research models and document study data. The role appeals to candidates seeking professional growth in a supportive, entrepreneurial environment that invests in employee development. While the position requires flexibility for schedule changes and occasional overtime, it offers a comprehensive benefits package and the opportunity to contribute to global life sciences safety and innovation.

This full-time role within the Late-Stage LNP Process Development team at Eurofins PSS focuses on laboratory studies to support process development, scale-up, and characterization of nucleic acid-based drug products. Key responsibilities include executing routine analytics such as dynamic light scattering and UV-quantification, performing bench-scale manufacturing experiments, and authoring technical documentation like SOPs and reports. The position offers a collaborative environment with opportunities for professional growth and work-life balance within a global life sciences leader. The role is based on-site in Boston, Massachusetts, with standard business hours and occasional overtime.