Jobs at Bridge Hotel Group

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 remote Project Manager role within the Early Phase team leads clinical research initiatives by coordinating Parexel and sponsor operations to ensure successful trial execution. Key responsibilities include managing end-to-end project lifecycles from pre-award strategy through close-out, overseeing budgets and timelines, and serving as the primary liaison for sponsors and internal functional teams. The position emphasizes risk management, regulatory compliance, and the development of tailored solutions for complex studies. The role appeals to professionals seeking a high-impact environment with a focus on operational excellence and professional growth. It offers the flexibility of a home-based arrangement with a preference for candidates located in California, Colorado, or Texas, fostering a culture of independent decision-making and strategic leadership within a global clinical research organization.

This 0.75 FTE Case Manager Liaison Nurse role focuses on ER discharge planning and inpatient care coordination for Kaiser Foundation Health Plan patients at St. Peter Hospital in Olympia. The position requires a Registered Nurse with prior case management experience to assess patient needs, develop comprehensive care plans, and facilitate seamless transitions to home health or long-term care facilities. Key responsibilities include collaborating with medical teams to optimize health outcomes, managing complex chronic disease cases, and ensuring appropriate resource utilization. The role offers a variable schedule with night shift differentials and alternating weekends, providing an opportunity to work within a collaborative environment that prioritizes patient advocacy and evidence-based care delivery.

This full-time Project Manager role within the Early Phase team leads clinical research initiatives for sponsors and internal functional groups. The position focuses on end-to-end project execution, including pre-award strategy, study start-up, and close-out procedures while ensuring compliance with ICH-GCP regulations. Key responsibilities involve managing project budgets and timelines, serving as the primary liaison for sponsors, and mitigating risks throughout the study lifecycle. The role offers the appeal of working with a high-performing team in a remote-friendly environment with a preference for California, Colorado, or Texas locations. It provides opportunities for professional growth through mentoring junior staff and contributing to standard operating procedure development.

The Business Development Specialist role supports strategic growth across the Americas region by partnering with Market Development leadership to execute regional sales and marketing initiatives. Key responsibilities include driving market expansion through strategic planning, managing key customer accounts, and coordinating cross-functionally with sales and product teams to align on project execution. The position also involves monitoring industry trends, supporting pricing strategies, and assisting with the localization of sales tools. This opportunity appeals to candidates seeking a collaborative environment where they can leverage their analytical and communication skills to influence global strategies while tailoring approaches to local markets. The role offers the chance to work with diverse teams across North and Latin America in a fast-paced setting focused on technical and commercial success.

This full-time weekend shift role serves as a Compliance Review Specialist within the Program Management Organization at an Aftermarket Service Center. The position acts as a vital bridge between customer requirements and operational execution, ensuring all product repairs strictly adhere to purchase orders, contracts, and FAA or military regulatory mandates. Key responsibilities include reviewing daily repair requirements for compliance, serving as a secondary point of contact for customer accounts, and identifying Value Added Services opportunities to drive business growth. The role also involves coordinating cross-functional problem-solving efforts and utilizing Lean Manufacturing principles to improve processes. This position appeals to candidates seeking a mission-driven environment focused on aerospace quality and operational excellence, offering opportunities for professional development through continuous improvement initiatives and a supportive benefits package.

The Customer Compliance Representative II role serves as a vital link between customer requirements and operational execution within the Aftermarket Service Center's Program Management Organization. Key responsibilities include reviewing repair requirements to ensure strict adherence to contracts and FAA regulations, acting as a secondary customer contact for repair status updates, and identifying Value Added Services to drive business growth. The position also involves coordinating cross-functional problem-solving efforts and applying Lean Manufacturing principles to improve processes. This opportunity appeals to candidates seeking a dynamic environment where technical compliance meets customer service excellence, offering a chance to contribute to high-stakes aerospace projects while supporting continuous improvement initiatives.

This full-time Customer Compliance Representative II role operates on the second shift within the Program Management Organization at an Aftermarket Service Center. The position acts as a vital bridge between customer requirements and operational execution, ensuring all product repairs strictly adhere to purchase orders, contracts, and FAA or military regulatory mandates. Key responsibilities include reviewing daily repair requirements for compliance, serving as a secondary customer contact for repair status updates, and identifying Value Added Services opportunities to drive business growth. The role also involves coordinating cross-functional problem-solving efforts and applying Lean Manufacturing principles to improve processes. This position is appealing for candidates seeking to work in a regulated aerospace environment with a focus on operational excellence and continuous improvement. The role requires strong organizational skills to manage multiple tasks in a fast-paced team setting while supporting critical aircraft on ground emergencies.

This full-time 2nd shift role within the Program Management Organization serves as a vital link between customer requirements and operational execution at the Aftermarket Service Center. The Compliance Review Specialist is responsible for reviewing repair requirements to ensure strict adherence to purchase orders, contracts, and FAA or military aerospace regulations. Key duties include acting as a secondary customer contact for repair status updates, identifying Value Added Services opportunities to drive business growth, and coordinating with Operations and Engineering to resolve complex technical issues. The position appeals to candidates seeking a collaborative environment where they can apply their problem-solving skills to support high-stakes aerospace projects. The role offers a structured career path within a regulated industry, emphasizing professional development and the opportunity to contribute to critical business growth initiatives.

The Project Manager - Early Phase role leads clinical trial initiatives for Parexel and its sponsors, focusing on operational excellence and strategic execution within the early development stage. Key responsibilities include managing the full project lifecycle from pre-award strategy and study start-up through implementation, risk mitigation, and close-out. The position requires overseeing budgets, ensuring regulatory compliance with ICH-GCP standards, and serving as the primary liaison for sponsors and internal teams. This opportunity appeals to professionals seeking a remote position with a preference for California, Colorado, or Texas locations, offering the chance to shape clinical research outcomes within a high-performing team. The role emphasizes leadership of virtual, cross-cultural teams and provides a platform for professional growth through involvement in complex project strategies and mentorship of junior staff.

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 full lifecycle of clinical sample collection, tracking, and destruction, while managing relationships with central laboratories and specialty vendors. The position also involves developing informed consent forms, coordinating logistics for sample testing, and ensuring compliance with study protocols and regulatory requirements. 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 experience in clinical research and laboratory sample management.

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 clinical sample collection, tracking, and destruction, 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, reviewing vendor invoices, and providing guidance to clinical sites on sample handling procedures. This opportunity appeals to professionals seeking to drive the translation of science into medicine within a collaborative environment. The role is based remotely and requires six to eight years of experience in clinical research laboratory management.

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 destruction, while managing relationships with central laboratories and specialty vendors. The position involves developing informed consent forms, coordinating logistics for human tissue and blood products, and ensuring compliance with study protocols and regulatory requirements. 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 and drive operational excellence in a dynamic biotech setting.

The Clinical Laboratory Study Manager role operates within the clinical research department to ensure high-quality sample and data delivery for biomarker evaluations. Key responsibilities include overseeing the entire lifecycle of clinical sample collection, processing, and storage, while managing relationships with central laboratories and specialty vendors. The position involves coordinating cross-functional teams to develop informed consent forms, monitor sample tracking, and ensure strict compliance with study protocols and regulatory requirements. This opportunity is appealing for professionals seeking to drive the translation of science into medicine within a collaborative environment that values operational excellence. The role is structured as a remote position, offering flexibility while maintaining close alignment with internal strategy leads and external partners.

This full-time Clinical Laboratory Study Manager role operates within the clinical research department to support precision medicine initiatives. The position involves overseeing the entire lifecycle of clinical samples, including collection, tracking, processing, and destruction, while ensuring strict adherence to informed consent and study protocols. Key responsibilities include managing relationships with central and specialty laboratory vendors, coordinating with cross-functional teams on data acquisition and transfer, and providing guidance to clinical sites on sample handling procedures. The role offers the appeal of working in a collaborative environment focused on translating scientific discoveries into medicine, with opportunities for professional growth in a remote work arrangement.

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, and destruction, while managing relationships with central laboratories and specialty vendors. The position involves developing informed consent forms, coordinating logistics for human tissue and blood products, and ensuring strict compliance with study protocols and regulatory requirements. 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 six to eight years of experience in clinical research lab management who excel at problem-solving and project coordination.

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 involves developing informed consent forms, coordinating logistics for human tissue and blood products, and ensuring compliance with study protocols and regulatory requirements. This opportunity appeals to professionals seeking to drive the translation of science into medicine within a collaborative environment. The role offers remote work flexibility and focuses on professional growth through complex project management and vendor oversight in the pharmaceutical industry.

This remote Project Manager role within the Early Phase team at Parexel leads clinical research initiatives by bridging sponsor and internal operational needs. The position involves managing the full project lifecycle from pre-award strategy and study start-up through implementation, risk mitigation, and close-out. Key responsibilities include serving as the primary sponsor liaison, overseeing budgets and timelines to ensure regulatory compliance, and mentoring junior team members. The role appeals to professionals seeking to shape clinical trial outcomes within a high-performing environment that values independent decision-making and strategic problem-solving. While based in California, Colorado, or Texas, the position offers significant flexibility for remote work and opportunities for professional growth in a global pharmaceutical setting.

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, tracking, and destruction, while managing relationships with central laboratories and specialty vendors. The position involves developing informed consent forms, coordinating logistics for human tissue and blood products, and ensuring strict compliance with study protocols and regulatory requirements. 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 six to eight years of experience in clinical research lab management who excel at problem-solving and project coordination.

The Project Manager - Early Phase role leads Parexel and sponsor teams to deliver tailored clinical research solutions from pre-award through study close-out. Key responsibilities include managing the full project lifecycle, including study start-up, budget oversight, risk mitigation, and ensuring compliance with ICH-GCP regulations. The position serves as the primary liaison for sponsors, coordinating cross-functional teams and driving operational excellence to meet timelines and quality standards. This opportunity appeals to professionals seeking a remote position with a preference for California, Colorado, or Texas, offering the chance to shape clinical trial outcomes within a high-performing team. The role emphasizes strategic decision-making, leadership of virtual global teams, and professional growth through involvement in complex early-phase programs.

This full-time Project Manager role within the Early Phase team leads clinical research initiatives by coordinating Parexel and sponsor operations to ensure successful trial execution. Key responsibilities include managing end-to-end project lifecycles from pre-award strategy through close-out, overseeing budgets and timelines, and serving as the primary liaison for sponsors and internal functional teams. The position requires independent decision-making to mitigate risks and maintain compliance with ICH-GCP regulations. The role appeals to professionals seeking a remote-first environment with a preference for California, Colorado, or Texas locations, offering the opportunity to shape clinical research outcomes within a high-performing global organization.

The Project Manager - Early Phase role leads clinical research initiatives by coordinating Parexel and sponsor teams to deliver trials on time and within budget. Key responsibilities include managing the full project lifecycle from pre-award strategy and study start-up through implementation, risk mitigation, and close-out. The position requires serving as the primary sponsor liaison, overseeing financial aspects like milestone payments, and ensuring compliance with ICH-GCP regulations. This opportunity appeals to professionals seeking a remote position with a preference for California, Colorado, or Texas locations, offering the chance to shape clinical research outcomes within a high-performing team. The role emphasizes leadership of virtual, cross-cultural teams and provides a platform for professional growth through involvement in strategic planning and mentorship of junior staff.