Trabajos cell therapy en Elizabeth, New JerseyCrear alertas

Job Description Shifts required and hours per week: (10-25 hours/week depening on the case) • We are looking for multiple therapists for multiple cases in the areas of Union, Linden, and Metuchen NJ, • Monday-Sunday morning, afternoon, & evening hours, • Potential daytime hours, • Hours subject to additional availability based on client needs, • Additional cases located in Linden & Metuchen with the following schedules:, • Linden, NJ:, • School Year Schedule:, • Friday (5pm - 8pm), • Saturday (11am - 2pm), • Sunday (11am - 4pm), • Summer Schedule:, • Wednesday (9am- 4pm), • Friday (5pm-8pm), • Saturday (11am-2pm), • Sunday (11am-3pm), • Metuchen, NJ:, • 2-3 days/week, year-round schedule, • Evening hours QUALIFICATIONS: • Required:, • Have a minimum of a Bachelor’s Degree, • Preferably in Education, Psychology or related field, • Minimum of 2 years of ABA experience., • Have access to a working cell phone, tablet, and/or laptop for data collections, • Possess a driver's license with reliable transportation and auto insurance for driving to clients., • Preferred:, • Have previous experience working with children and/or managing challenging behaviors with children., • CPI Certification (Crisis Prevention Intervention), • Alternatively, Successful completion of Safety Care/Handle With Care Training., • Be able to play and engage children., • Excellent interpersonal and communication skills - spoken and written., • Be CPR and First Aid certified. BENEFITS: • Flexible schedule, • Professional development assistance (RBT & Student BCBA supervision hours), • Health Insurance (Medical), • 401K Matching, • Paid Time Off, • Training and assessments to become successful Behavior Technicians/RBT., • Our training programs and evaluation systems are aligned with the standards for this credential per the Behavior Analyst Certification Board© PHYSICAL REQUIREMENTS: • Walking, occasional running, standing, sitting, kneeling, stooping, crouching, crawling, twisting, reaching above head, pulling, bending, and carrying up to 50 pounds., • Work may involve playing with children that can occur on the floor or settings where the furniture is child-size., • Diligently attending to the safety of the patient and surroundings is required., • Quick and sudden movements may be required., • Sustained physical exertion may be required for up to 45 minutes. JOB DESCRIPTION: • Under the supervision of a Board Certified Behavior Analyst©, the Behavior Therapist provides Applied Behavior Analysis, ABA, therapy services for children diagnosed on the autism spectrum. The Behavior Technician will:, • Implement programs based on ABA principles increasing communication, self-help, social and play skills., • Keep clients motivated to learn and provide reinforcement for achieved skills., • Accurately keep a record of client’s progress., • Manage challenging behaviors that occur., • Maintain confidentiality of client information., • Travel to client’s homes/community settings, as required for service delivery. Learn more about us: www.emittherapeutics.com \nCompany Description At EMIT Therapeutics, we're changing lives through compassionate, individualized, evidence-based ABA therapy. Our team empowers children and teens with autism to build meaningful communication, independence, and lifelong skills while reaching their fullest potential. We invest in our employees and foster a collaborative, supportive culture where clinicians are valued, mentored, and encouraged to grow professionally. If you're passionate about making a lasting impact while advancing your career, EMIT Therapeutics is the place for you. At EMIT Therapeutics, we're changing lives through compassionate, individualized, evidence-based ABA therapy. Our team empowers children and teens with autism to build meaningful communication, independence, and lifelong skills while reaching their fullest potential. We invest in our employees and foster a collaborative, supportive culture where clinicians are valued, mentored, and encouraged to grow professionally. If you're passionate about making a lasting impact while advancing your career, EMIT Therapeutics is the place for you.

\n American Traveler is seeking a travel nurse RN Oncology for a travel nursing job in Newark, New Jersey. Job Description & Requirements\n \n • Specialty: Oncology\n, • Discipline: RN\n, • Start Date: 09/21/2026\n, • Duration: 13 weeks\n, • 37 hours per week\n, • Shift: 8 hours, days\n, • Employment Type: Travel\n \n Assignment Overview\n \n • Shift: Days, 5x7.5hrs\n, • Hours: 37.5 hrs/wk\n, • Start Date: Sep 21, 2026\n, • Length: 13 weeks\n, • Openings: 1\n Description\n American Traveler is hiring an experienced Oncology RN for a 13-week day shift assignment requiring at least one year of medical oncology experience and an active NJ or Compact RN license. Details\n \n • Adult medical oncology unit treating GI, GU, breast, head and neck, neuro, thoracic, lymphoma, and leukemia patients\n, • Also cares for GYN oncology and classic hematology patients (sickle cell, anemia, factor 8, ITP)\n, • Performs bone marrow biopsies, paps, biopsies, colposcopy, and pelvic exams in clinic setting\n, • Day shift schedule, 5x7.5-hour shifts, 37.5 hours per week\n, • Epic EMR experience required\n, • Floating required within skillset, with ratios varying based on census and patient acuity\n Requirements\n \n, • Active NJ or Compact RN license required\n, • BLS certification required\n, • Minimum 1 year of medical oncology nursing experience required\n, • Epic charting experience required\n, • Skilled in accessing and managing ports, central line blood draws, and PICC line care\n, • Experience administering Neupogen, hormonal therapy, and coagulation factors\n, • Colostomy care experience required\n, • Knowledge of oncologic emergencies including tumor lysis syndrome, anaphylaxis, extravasation, hemorrhage, sepsis, and spinal cord compression preferred\n, • Experience managing symptoms such as nausea/vomiting, neuropathy, dysphagia, and altered mental status\n, • SSN and DOB required for consideration\n, • Two current professional references required\n Additional Information\n \n, • Provide direct patient care across a wide range of oncology diagnoses including breast, lung, colorectal, and blood cancers\n, • Deliver psychosocial support including advanced directives, patient/family education, and symptom management\n, • Administer pain management therapies including IV push narcotics and transdermal patches\n, • Perform wound care, tracheostomy management, and neutropenic precautions\n, • Must be available to work 2 of 3 major holidays\n, • Requested time off must be confirmed and submitted prior to consideration; RTO requests after an offer will not be accommodated\n, • Assignment is expected to serve as the traveler's primary work commitment\n, • Local candidates accepted at the same pay rate\n, • Former RWJBH staff (full-time or PRN) must have been separated from the health system for at least one year to be eligible\n, • Open or active background/license hits are not accepted\n, • Labs must be completed within 48 hours of signing\n, • International work history or permanent residency must be disclosed\n \n \n American Traveler Job ID #P-743240. Pay package is based on 8 hour shifts and 37 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Travel RN - Med/Surg - Oncology About American Traveler\n \n With over 25 years of experience, American Traveler has established a reputation for outstanding customer service. Our team ensures a smooth, worry-free experience for those starting on or expanding their travel nursing and allied careers. \n With thousands of travel nursing and allied jobs nationwide, our attentive and approachable recruiters find positions that align perfectly with your career aspirations and personal requirements. \n American Traveler offers exceptional benefits, including premium medical, dental, vision and life insurance beginning day one of your assignment, generous 401(k) match, substantial housing stipends, and more. Additionally, with 24/7 support and access to our in-house clinicians, you are assured confidence and comfort throughout your assignment. \n With our team behind you, you can relax and enjoy a rewarding travel career. \n \n \n

Job Description Job Title: Sales Development Representative (SDR) Location: Jersey City, NJ Hours / Schedule: 9AM–5PM or 10AM–6PM (Monday–Friday), Onsite Type: Direct Hire Compensation: $70,000 annually + commission (5% New Clients / 4% Recurring & Dormant Orders) A great opportunity to work for a global leader in medical biotechnologies, specializing in cellular therapies and regenerative medicine. We are seeking a talented and competitive Sales Development Representative (SDR) who thrives in a medical device sales environment. Requirements • 3–5 years of experience with an Inside Sales ., • Minimum 1 year of Salesforce experience or equivalent CRM platform., • Scientific, clinical, or business background., • Sales experience in the pharmaceutical, medical device, or related industries., • Experience with medical device terminology and product discussions., • Ability to complete a fast paced training program that covers learning about exciting PRP and regenerative therapy products and how to communicate effectively with clients / prospects. Responsibilities, • Perform a variety of tasks to deliver exceptional customer service while driving sales., • Complete a fast paced training program covering:, • Company products including PRP, cell therapies, and related kits, • KPI expectations and sales targets, • Effective communications with clients and prospects, • Contact new leads generated through outbound calling programs to present company products., • Follow up with prospective and active clients; document status and action plans in the CRM., • Listen to customer concerns/complaints and provide detailed information about products and services., • Present customers with additional information on new products and service offerings., • Determine the quickest, most effective method for responding to client questions. Benefits: Comprehensive and Competitive Benefits Package including health benefits, PTO and generous commissions. #M3 Ref: #558-Scientific

Quantifies and maintains materials in production dispensary. Maintains timing according to the production schedule to ensure on-time logistics. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those

The Label Operations Manager at the S12 Cell Therapy manufacturing facility is responsible for implementing and managing the site Label Operations activities at S12 Summit West (Summit, NJ) in accordance with BMS policies, standards, procedures and Global cGMPs. Functional responsibilities include supervision of all label control activities for Cell Therapy Development and Operations (CTDO); Responsible for developing and maintaining a GMP compliant clinical and commercial label issuance and control process. The Label Operations organization is responsible for the establishment, maintenance and continuous improvement of the clinical and commercial label control process, procedures, and responsibilities for achieving quality policies and objectives. This organization supports the S12 facility to ensure patient safety, regulatory requirements and improve its effectiveness and efficiency on a continuous basis. Shift Available: • Wednesday - Saturday, Onsite Night Shift, 6 p.m. - 4:30 a.m. Responsibilities: • The Label Operations manager will lead team to ensure Label Management and align with Global and Regional Regulatory requirements., • Manage and motivate team members, build trust and cultivate a collaborative environment., • Oversee team responsibilities and maintain a state of compliance., • Work proactively to identify and address any label control compliance issues., • Oversees, supervises, coordinates and prioritizes daily activities of the Label Operations team located at Summit, NJ S12 facility., • Act as site lead for clinical and commercial label management related system implementation initiatives. Fully support projects within project timelines., • Assures job objectives are met on a timely basis., • Assures timely issuance of clinical and commercial in-process and final product labels for labeling operations., • Coordinates and prioritizes project deliverables to support new drug product launches, new market and other quality management activities as assigned., • Creates employee development plans, and oversight of functional area to assure adequate staffing., • Coach and mentor subordinates in the areas of training, disciplinary action, problem solving, and professional growth., • Provide support for activities using the electronic label issuance and control systems., • Assures standard operating procedures (SOPs) related to job responsibilities define the steps necessary to complete tasks, etc. Writes, reviews and updates SOPs while managing archival of batch records and GMP documentation for the site., • Perform gap assessments to identify process deficiencies, provide reports to document detailed findings and recommend potential solutions., • Develops and maintains quality metrics to monitor compliance., • Collaborates with stakeholders to develop appropriate actions to resolve quality system issues., • Responsible for developing, managing, and on-boarding requirement for new staff within label control., • Maintains current knowledge of industry standards as it applies to cGMPs and global regulatory guidelines and requirements., • Performs supplemental investigations/projects as required by management. Knowledge & Skills: • Must have advanced GMP, Quality, compliance and risk management knowledge., • Must be able to interpret problems and effectively prepare surrounding communication in a productive manner to management and to the group with clarity, brevity, and accuracy., • Provide guidance to other employees in the interpretation of compliance and technical/scientific issues across most of the job function. Develop employees and coach them to bridge knowledge gaps., • Must have strong authorship and able to critically review reports while effectively providing input and expressing Quality Risk management principles., • Must be action-oriented, customer-focused and skilled in decision-making, building relationships, problem solving, conflict management, planning and organizing, resource allocation, and analytical thinking., • Must be skilled in coaching others, talent selection, developing others, decision-making, building relationships, innovation management, and resource allocation., • Must possess an independent mindset and tenacity., • Leads teams and cross-functional project teams and drives team performance and results. Contributes highly to departmental performance and quality initiatives; able to conceptualize impact of quality initiatives in terms of cross-functional teams; emerging as a leader contributing to BMS culture and values., • Demonstrated proficiency with PC-based office computers and standard Microsoft Office applications., • Requires minimal direction to completes tasks, knows how to get resources and information from established internal contacts; consults with manager for decisions outside established processes; manages experienced professional employees; authority to make daily decisions that impact their team., • Effectively communicates internally within the function and with internal and external cross-functional teams. Interacts with internal and external cross-functional teams. Represents department in internal and external cross-functional teams., • Routinely recognizes and resolves quality issues informs management of proposed solutions. Seeks management guidance on complex issues. Develops procedures. Minimum Requirements: • B.S. Degree required. Equivalent combination of education and experience will be considered., • Minimum 5 years relevant work experience., • Minimum 2 years of leadership experience. Working Conditions: • Work is performed in a typical office environment, with standard office equipment available and used., • Work is generally performed seated but may require standing and walking for up to 10% of the time., • Lighting and temperature are adequate and there are no abnormal conditions caused by noise, dust, etc. Compensation Overview: Summit West - NJ - US: $103,560 - $125,495 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include: • Health Coverage: Medical, pharmacy, dental, and vision care., • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP)., • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. Work-life benefits include: Paid Time Off • US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees), • Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. *Eligibility Disclosure: T he summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Contractors, leased workers and other service providers are not eligible to participate in the program. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as "Transforming patients' lives through science ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring

ERP Implementation Site Data Lead.This role will support the implementation of a new ERP system across multiple cell therapy facilities in northern New Jersey.The site data lead will immerse themselves within these sites and with global functions to complete data cleansing, build standardization, an

Associate Director, CAR-T Site Supply Chain Product Planner. The Associate Director CAR-T Site Supply Chain Product Planner is a planning role in the Cell Therapy Operations Summit West (CTO SMVV) New Jersey manufacturing site. This role will report directly to Supply Planning Director and sit on th

The Field Applications Scientist (FAS) is a key member of Miltenyi's Commercial Sales team, playing a central role in customer success across flow cytometry, imaging, and clinical cell and gene therapy manufacturing platforms. Support resolution of complex technical problems, including coordination

Location: Cell Therapy Operations, Summit, New Jersey.Purpose And Scope Of Position: This role is responsible for working on New Hire Orientation Program (NHOP) for the Summit West Cell Therapy Operations organization, as well as the accurate and timely processing of all training requests related to

From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. The Manager, CSV Cell Therapy supports the successful implementation and support of manufacturing and laboratory equipment and comput

A great opportunity to work for a global leader in medical biotechnologies, specializing in cellular therapies and regenerative medicine. We are seeking a talented and competitive Sales Development Representative (SDR) who thrives in a medical device sales environment. • 35 years of experience with an Inside Sales., • Minimum 1 year of Salesforce experience or equivalent CRM platform., • Scientific, clinical, or business background., • Sales experience in the pharmaceutical, medical device, or related industries., • Experience with medical device terminology and product discussions., • Ability to complete a fast paced training program that covers learning about exciting PRP and regenerative therapy products and how to communicate effectively with clients / prospects., • Perform a variety of tasks to deliver exceptional customer service while driving sales., • Complete a fast paced training program covering:, • Company products including PRP, cell therapies, and related kits, • KPI expectations and sales targets, • Effective communications with clients and prospects, • Contact new leads generated through outbound calling programs to present company products., • Follow up with prospective and active clients; document status and action plans in the CRM., • Listen to customer concerns/complaints and provide detailed information about products and services., • Present customers with additional information on new products and service offerings., • Determine the quickest, most effective method for responding to client questions. Benefits: Comprehensive and competitive benefits package including health benefits, PTO and generous commissions.

Senior Project Manager Cell Therapy Development and Operations will influence and manage all aspects of initiating, planning, and executing complex, multi-disciplinary projects throughout the projects' lifecycle. Ensure the project teams for the assigned projects are following the current standards

Program Manager, Cell Therapy Supply Chain Capabilities. Bachelor's Degree in Supply Chain, Manufacturing, Information Systems, Business, Engineering or similar area.

The Project Management Specialist of CPV & CI, within the MSAT organization, will support the project timelines, to support the Summit, NJ Cell Therapy facility.The Project Specialist provides project management support ensuring projects are executed within established quality metrics, budgets, and

Minimum of five (5) years of business experience, preferably with multi-disciplined procurement experience or related category domain experience is required. Procurement process knowledge, contract management, financial analysis, market analysis, supplier management, strategic planning and integrate

Working with Us Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. The TAIP TA Lead is a senior leadership role reporting directly to the Head of the TAIP unit within Bristol Myers Squibb's Trial Analytics, Insights, and Planning (TAIP) organizationan internal consulting team that drives clinical development excellence through data-driven insights, feasibility modelling, and strategic trial planning. As the analytics lead for the Oncology therapeutic area (TA), you will be accountable for the end-to-end analytics strategy and execution across a global portfolio of clinical trials within that TAsupporting trial-level planning, overseeing delivery performance, and leading a team of analytics professionals across multiple levels and geographies. This role will have direct reports across different levels of seniority, and the incumbent will provide day-to-day direction, coaching, and performance management. You will serve as a strategic thought partner to TA medical, clinical, and operational leadership, influencing decisions that directly impact trial timelines, cost, and quality. You will be responsible for providing hands-on support, and quality control across studies while coaching study-level analytics leads and coordinating cross-trial priorities. You will act as a sounding board and escalation point for delivery-focused team members and serve as a trusted partner to TA medical, clinical, and operational leadership. This role requires a strong foundation in both clinical trial science and applied analytics across site feasibility, enrollment modeling, scenario exploration, along with the ability to translate insights into strategies that directly impact trial timelines and operational delivery outcomes. You will play a key role in evolving TAIP capabilities, ensuring consistency across analytic methodology, fostering innovation, and driving measurable business impact. • Manage a team of analysts, including accountability for performance management, career development, and day-to-day support, • Lead the analytics strategy and execution across a global portfolio of oncology trials, • Guide, support, and review work across study-level analytics leads, acting as both coach and strategic sounding board, • Track delivery progress across trials, escalating risks and ensuring alignment with trial milestones and enterprise priorities, • Serve as a strategic advisor to TA leadership, shaping trial strategy, feasibility, and portfolio-level planning through data-driven insights, • Ensure cross-trial consistency and innovation in forecasting, feasibility modelling, performance dashboards, and protocol analytics, • Promote global collaboration, coordinating across teams to ensure effective, scalable delivery, • Lead discussions on cost implications of country mix and study design decisions at the portfolio level, • Promote study optimization analytics across trials, including evaluation of patient and site burden and competitive landscape data, • Coordinate field-based insights into TA-wide feasibility and site prioritization approaches, • Champion use of platforms, tools, and data infrastructure that support delivery excellence, • Integrate analytics with clinical supply planning where relevant to ensure delivery-readiness, • Contribute to the enterprise evolution of TAIP, defining best practices, mentoring talent, and elevating analytics standards across trials, • Applies critical thinking to analyze complex data, challenge assumptions, and generate strategic, evidence-based recommendations Education: • Advanced degree (MBA, MSc, MPH, PharmD, PhD, or equivalent) in a relevant field preferred such as Biology, Medicine, Data Science, Computer Science, Clinical Research, etc. Experience: • 10+ years in management consulting, trial analytics, or clinical strategy is required, • Direct experience with clinical trial feasibility, enrollment forecasting, and operational analytics, • Deep experience in Oncology or related fields, • Proven ability to lead teams, engage with senior stakeholders, and operate effectively across global functions, • Demonstrated experience delivering under tight timelines and comfortable operating in a fast-paced environment Skills: • Strategic and analytical thinker with the ability to translate data-driven insights into enterprise-level decisions, • Excellent leadership, communication, and stakeholder management skills, • Direct experience with building forecasting models, dashboards, and site feasibility tools is a plus, • Drive strategic clinical impact: Leverage data, analytics, and scientific expertise to inform smarter, faster development decisions that bring therapies to patients sooner, • Shape the future of analytics leadership: As member of the TAIP leadership team, you will help define the future of trial analytics at BMSsetting standards, mentoring talent, and influencing the evolution of data-driven trial planning across the enterprise, • Pathway to enterprise leadership: This role is a launchpad for broader strategic and leadership opportunities across BMS, • Collaborate globally, drive locally: Operate as part of a distributed team while anchoring analytics leadership within your therapeutic area If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Compensation Overview: Cambridge Crossing: $261,840 - $317,292 & Princeton - NJ - US: $233,780 - $283,291 The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience. Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/. Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include: • Health Coverage: Medical, pharmacy, dental, and vision care., • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP)., • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support. ? Work-life benefits include: Paid Time Off • US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees), • Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown. *Eligibility Disclosure: T he summer hours program is for United States (U.S.) office

Project Coordinator position provides project coordination support for executive leaders and/or their respective leadership teams. Serve as project coordinator for key projects scoping Cell Therapy Operations. Proven track record of collaboration with project/program managers and/or other project co

The Specialist, Planning and Master Data will be responsible for creating, updating, and maintaining master data elements supporting Client' Cell Therapy treatment center account management. Experience in planning/scheduling, managing operations, and/or managing master data in a supply chain or pati

Job DescriptionAt LifeStance Health, we believe in a truly healthy society where mental and physical healthcare are unified to make lives better. Our mission is to help people lead healthier, more fulfilling lives by improving access to trusted, affordable, and personalized mental healthcare. Everywhere. Every day. It’s a lofty goal; we know. But we make it happen with the best team in behavioral health. Thank you for taking the time to explore a career with us. As the fastest growing behavioral health practice group in the country, now is the perfect time to join our clinical team! We are actively looking to hire talented PMHNP-BCs in the Jersey City, NJ area who are passionate about patient care and committed to clinical excellence. *The tentative start date for this position is July 2026* Is This You? • Wanting to deliver high quality behavioral healthcare., • Seeking work life balance., • Interested in growing professionally., • Uncapped earning potential, • Generous sign-on bonus, • BenefitsWhat we offer Nurse Practitioners:, • The ability to work closely with the adult and child/adolescent populations., • Flexible work schedules., • Telemedicine and in-person flexibility at the present time., • Generous ‘above market’ compensation with unlimited/uncapped earnings., • Full benefits package: health, dental, vision, life, 401k (with match), paid parental leave, holidays, EAP and more., • Collegial work environment., • Newly designed and modern offices., • Full administrative support., • Latest in digital technology., • Strong work/life balance., • Earnings annually in the range of $130,000 - $200,000+ compensation model based on productivity Nurse Practitioners are a critical part of our clinical team. We’re seeking Nurse Practitioners that are:, • Licensed in New Jersey with a Psychiatric Mental Health Nurse Practitioner Certification (PMHNP-BC) and holding an active DEA., • Experienced in both medication management as well as therapy., • Must be able to see child and adolescent populations., • New grad welcome to apply (with previous RN experience in psychiatry). Jenni GreeneDirector, Practice DevelopmentLifeStance Health, Inc.(cell): 754-224-7079(email): Jennifer.Greene@LifeStance.com About LifeStance Health LifeStance is a national provider of mental healthcare services focused on evidenced-based, medically driven treatment services for children, adolescents and adults suffering from a variety of mental health issues in an outpatient care setting, both in-person at its clinics nationwide and through its digital health telemedicine offering. The company employs psychiatrists, psychologists, psychiatric nurse practitioners, and licensed therapists throughout the US. LifeStance Health is an equal opportunity employer. We celebrate diversity and are fully committed to creating an inclusive work environment for all our employees. Our values:Belonging: We cultivate a space where everyone can show up as their authentic self.Empathy: We seek out diverse perspectives and listen to learn without judgment.Courage: We are all accountable for doing the right thing - even when it's hard - because we know it's worth it.One Team: We realize our full potential when we work together towards our shared purpose. If you elect to interact with us via our website, please only use www.lifestance.com or www.careers.lifestance.com. Additionally, our recruiters utilize email addresses with the @lifestance.com domain. Other websites and domains are not affiliated with LifeStance Health and may represent threats to your data security. LifeStance Health complies with federal and state disability laws and makes reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact our Human Resources Team at ADA@lifestance.com or by calling +1-800-308-0994. Please note: This contact is intended solely for accommodation requests. Inquiries regarding applications, resumes and applicant status should not be sent to this email address as they will not be reviewed or responded to. To apply for a position, please use our official careers page.

The Senior Project Manager, Cell Therapy Cross Functional Capabilities (Senior Project Manager) is responsible for planning and delivery of Cell Therapy operations projects, programs, and/or business system releases as assigned. The Senior Project Manager will work with cross-functional business uni