907 Drug jobs in the United States

This position is on-site 4 days per week and 1 day from home. A remote position is not possible for this role.
**The Manager Development Program Management** provides operational direction as the leader for one or more development programs. Manager Development Program Management executes the strategic direction of a program from preclinical through commercialization by driving the development and implementation of integrated program plans, goals, budgets, and timelines. The Manager Development Program Management is responsible for forming and managing effective cross functional teams and leads a network of functional area project managers.
**In a typical day you will:**
+ Support development of a program throughout its lifecycle, by integrating key stakeholders from Discovery, Manufacturing, Preclinical, Global Development and Commercial. Independently manages multiple development programs, often working under consultative direction.
+ Partner with the Strategic Program Lead to provide operational leadership of program (s) and supports development and execution of overall program strategy by facilitating cross functional Strategic Development Team. Assesses and proactively addresses the needs of the program from pre-IND through commercialization and makes operational decisions to support requirements for success. Actively aims to strengthen and lead high performance teams.
+ Lead annual goal setting sessions to develop project / program level goals that align with Regeneron's overall goals and monitors progress against these goals.
+ Develop contingency and risk mitigation plans. Oversees the development of integrated project / program plans and actively monitors progress against the approved baselines. Responsible for oversight of the integrated program timeline and budget, including management of variances and escalation where appropriate.
+ Manage the project / program interactions and deliverables between Regeneron and our strategic alliance partners and collaborators (where applicable). Fosters collaborative relationships across the alliance program teams to develop and execute strategic development plans.
**This role may be for you if you:**
+ Have excellent written, verbal and interpersonal communication skills
+ Can motivate others and build effective teams.
+ Possess strong critical thinking skills.
+ Can make connections and relate details to broader program strategy and goals.
+ Resolve and negotiate conflicts or problems with tact, diplomacy and composure.
+ Are highly organized, and have solid time management skills (both project and self), with ability to manage multiple priorities.
**In order to be considered for this opportunity** , you must have a BS or MS degree with at least 7+ years of relevant broad project/program management experience required, preferably in the pharmaceutical or related industry and drug development. Specific experience managing the development strategy for a drug candidate is necessary.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
**Salary Range (annually)**
$113,100.00 - $184,700.00

_This position is on-site in Tarrytown, NY 4 days a week and 1 day from home. A fully remote role is not possible for this position._
Using extensive program management knowledge and experience in the drug development industry, the **Director, Development Program Management** provides operational leadership, direction and support to a team, program or project of moderate to large scope, (within a given Therapeutic Area) as well as to the DPM department as a whole. The Director, Development Program Management executes the strategic direction of a program from preclinical through commercialization by driving the development and implementation of integrated (project) program plans, goals, budgets, and timelines. Director, Development Program Management is responsible for the successful operation of activities of major significance to the organization.
**In a typical day you will:**
+ Provide operational leadership, direction and support of a program throughout its lifecycle, by integrating key stakeholders from Discovery, Manufacturing, Preclinical, Global Development and Commercial.
+ Independently lead multiple or complex development programs.
+ Partner with the Strategic Program Lead to provide operational leadership of program(s) and supports development and execution of overall program strategy by facilitating cross-functional Strategic Development Team. Independently assesses and proactively addresses the needs of the program from pre-IND through commercialization and makes operational decisions to support requirements for success. Strengthens and leads high performance teams.
+ Leverage significant project management experience and knowledge of the drug development process, drives team alignment in creation of integrated project / program plans, timelines and budgets. Ensures efficient delivery of plans. Directs annual program goal setting in alignment with Regeneron's overall goals and monitors progress against these goals. Champions potential program risks and ensures contingency plans are in place.
+ Act as a key liaison between Regeneron and our strategic alliance partners and collaborators (where applicable). Prepares, provides input, and / or manages the process involving major presentations for collaboration meetings effecting key business decisions. Responsible for facilitating and driving decision making in support of the joint strategic objectives of the program.
+ **Communication:** Ensures effective, accurate, and timely scientific / technical program-related communication to the team and Sr. Management. Adept at tailoring communications based on audience, effectively framing and communicating nuanced context for stakeholders and capturing rationale for decisions.
**This role may be for you if you:**
+ Have excellent written, verbal and interpersonal communication skills and the ability to effectively interact with all levels both within and outside the company in order to establish credibility with professionals on the project teams.
+ Understand and motivate others and build effective teams.
+ Have strong presentation and critical thinking skills.
+ Actively promote constructive interactions among team members in order to address difficult situations.
+ Resolve and negotiate conflicts or problems with tact, diplomacy and composure.
+ Handle multiple projects and priorities with exceptional organizational and time management skills (both project and self)
+ Thrive in fast paced organizations; expert in dealing with ambiguity and uncertainty
**In order to be considered qualified** , you must have a Bachelor's degree and 12+ years of in-house pharmaceutical program management with knowledge of the drug development process as well as understanding of clinical trials.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
**Salary Range (annually)**
$180,400.00 - $300,700.00

Our client is a cutting-edge pharmaceutical company dedicated to advancing human health and is seeking an exceptional Senior Formulation Scientist to join our fully remote drug development team. This is a unique opportunity to contribute to the design, development, and optimization of novel drug formulations from the comfort of your home office. You will play a critical role in translating scientific discoveries into viable therapeutic products, working with a team of world-class researchers and developers.

Responsibilities:

• Design and execute studies for the formulation development of small molecules, biologics, or other therapeutic modalities.
• Develop robust and scalable manufacturing processes for various dosage forms (e.g., oral solids, injectables, topical).
• Characterize formulations using a range of analytical techniques (e.g., HPLC, GC, dissolution testing, physical property measurements).
• Troubleshoot formulation and process-related issues, implementing effective solutions.
• Conduct pre-formulation studies to assess drug substance properties and guide formulation strategy.
• Write comprehensive development reports, protocols, and regulatory submission documents.
• Collaborate closely with cross-functional teams, including analytical development, CMC, process engineering, and regulatory affairs.
• Stay abreast of emerging technologies and trends in pharmaceutical formulation and drug delivery.
• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
• Mentor junior scientists and contribute to a collaborative and innovative research environment.
• Manage external research collaborations and vendor relationships as needed.
• Present scientific findings at internal meetings and potentially at external conferences.

Qualifications:

• Ph.D. or Master's degree in Pharmaceutical Sciences, Chemical Engineering, Chemistry, or a related field.
• Minimum of 5 years of progressive experience in pharmaceutical formulation development.
• Proven track record in developing various dosage forms and optimizing drug delivery systems.
• Hands-on experience with a wide array of formulation development techniques and analytical methods.
• Strong understanding of CMC principles and regulatory requirements for drug development.
• Excellent problem-solving, critical-thinking, and experimental design skills.
• Proficiency in scientific writing and documentation.
• Exceptional communication and interpersonal skills, with the ability to collaborate effectively in a distributed team setting.
• Experience with small molecules and/or biologics is desirable.
• Familiarity with QbD (Quality by Design) principles.

This remote position offers the chance to work on impactful drug development projects and contribute to life-changing therapies. If you are a highly skilled and motivated formulation scientist seeking a challenging remote role, we encourage you to apply.

Job Description

The Food Service Worker will assist the manager with food/meal preparation; maintain cash receipts and meal records. Assist manager in completing daily reports. Maintain high standards of quality in food production, sanitation, and kitchen safety practices.

Job Responsibilities

• Prepare quality food and baked goods according to a planned menu
• Prepare a daily report that verifies transactions
• Understand what is inclusive of a meal
• Ensure storage of food in an accurate and sanitary manner
• Serve food according to meal schedules, department policies and procedures
• Use and care of kitchen equipment, especially knives
• Timely preparation of a variety of food items, beverages, and
• Add garnishments to ensure customer happiness and eye appeal
• Coordinate and assist in major cleaning of refrigerators, freezers, and cooking and serving equipment
• Adhere to all food safety regulations for sanitation, food handling, and storage
• Adhere to the uniform policy
• Connect with the Manager daily to understand and accurately prepare menu for the day
• Supervise the food temperature requirements
• Maintain a clean and organized work and storage area
• Scrub and polish counters, clean and sanitize steam tables, and other equipment
• Follow established procedures and standards for cleanliness, to ensure a balanced and safe environment; duties include sweeping, moping, ware washing
• Maintain garbage collection site and kitchen floor areas in a neat and sanitary fashion
• Perform other duties as assigned including other areas in the kitchen
• This role may have physical demands including, but not limited to, lifting, bending, pushing, pulling and/or extended walking and standing. This role may also require uniforms and/or usage of Personal Protective Equipment (PPE).
  

At Aramark, developing new skills and doing what it takes to get the job done make a positive impact for our employees and for our customers. In order to meet our commitments, job duties may change or new ones may be assigned without formal notice.

Qualifications

• Food Service Certificate as needed
• Sufficient education or training to read, write, and follow verbal and written instructions
• Be able to work quickly and concisely under pressure

Education About Aramark

Our Mission

Rooted in service and united by our purpose, we strive to do great things for each other, our partners, our communities, and our planet.

At Aramark, we believe that every employee should enjoy equal employment opportunity and be free to participate in all aspects of the company. We do not discriminate on the basis of race, color, religion, national origin, age, sex, gender, pregnancy, disability, sexual orientation, gender identity, genetic information, military status, protected veteran status or other characteristics protected by applicable law.

About Aramark

The people of Aramark proudly serve millions of guests every day through food and facilities in 15 countries around the world. Rooted in service and united by our purpose, we strive to do great things for each other, our partners, our communities, and our planet. We believe a career should develop your talents, fuel your passions, and empower your professional growth. So, no matter what you're pursuing - a new challenge, a sense of belonging, or just a great place to work - our focus is helping you reach your full potential. Learn more about working here at or connect with us on Facebook, Instagram and Twitter.

**Job Description**
The Food Service Worker will assist the manager with food/meal preparation; maintain cash receipts and meal records. Assist manager in completing daily reports. Maintain high standards of quality in food production, sanitation, and kitchen safety practices.
**Job Responsibilities**
+ Prepare quality food and baked goods according to a planned menu
+ Prepare a daily report that verifies transactions
+ Understand what is inclusive of a meal
+ Ensure storage of food in an accurate and sanitary manner
+ Serve food according to meal schedules, department policies and procedures
+ Use and care of kitchen equipment, especially knives
+ Timely preparation of a variety of food items, beverages, and
+ Add garnishments to ensure customer happiness and eye appeal
+ Coordinate and assist in major cleaning of refrigerators, freezers, and cooking and serving equipment
+ Adhere to all food safety regulations for sanitation, food handling, and storage
+ Adhere to the uniform policy
+ Connect with the Manager daily to understand and accurately prepare menu for the day
+ Supervise the food temperature requirements
+ Maintain a clean and organized work and storage area
+ Scrub and polish counters, clean and sanitize steam tables, and other equipment
+ Follow established procedures and standards for cleanliness, to ensure a balanced and safe environment; duties include sweeping, moping, ware washing
+ Maintain garbage collection site and kitchen floor areas in a neat and sanitary fashion
+ Perform other duties as assigned including other areas in the kitchen
+ This role may have physical demands including, but not limited to, lifting, bending, pushing, pulling and/or extended walking and standing. This role may also require uniforms and/or usage of Personal Protective Equipment (PPE).
At Aramark, developing new skills and doing what it takes to get the job done make a positive impact for our employees and for our customers. In order to meet our commitments, job duties may change or new ones may be assigned without formal notice.
**Qualifications**
+ Food Service Certificate as needed
+ Sufficient education or training to read, write, and follow verbal and written instructions
+ Be able to work quickly and concisely under pressure
**Education**
**About Aramark**
**Our Mission**
Rooted in service and united by our purpose, we strive to do great things for each other, our partners, our communities, and our planet.
At Aramark, we believe that every employee should enjoy equal employment opportunity and be free to participate in all aspects of the company. We do not discriminate on the basis of race, color, religion, national origin, age, sex, gender, pregnancy, disability, sexual orientation, gender identity, genetic information, military status, protected veteran status or other characteristics protected by applicable law.
**About Aramark**
The people of Aramark proudly serve millions of guests every day through food and facilities in 15 countries around the world. Rooted in service and united by our purpose, we strive to do great things for each other, our partners, our communities, and our planet. We believe a career should develop your talents, fuel your passions, and empower your professional growth. So, no matter what you're pursuing - a new challenge, a sense of belonging, or just a great place to work - our focus is helping you reach your full potential. Learn more about working here at or connect with us on Facebook , Instagram and Twitter .

Our client, a leading innovator in pharmaceutical research and development, is seeking a highly motivated and experienced Senior Research Scientist to join their dynamic oncology drug development team. This role is based in a state-of-the-art facility located in **Chicago, Illinois, US**, offering a hybrid work model to balance collaborative in-office efforts with focused remote work.

The successful candidate will play a pivotal role in the discovery and preclinical development of novel therapeutic agents for cancer treatment. This involves designing and executing complex experiments, analyzing data, and contributing to the strategic direction of drug discovery programs. You will be responsible for leading research projects, mentoring junior scientists, and collaborating with cross-functional teams including medicinal chemistry, pharmacology, and regulatory affairs.

Key Responsibilities:

• Design, develop, and optimize in vitro and in vivo assays to evaluate drug efficacy and safety.
• Conduct detailed data analysis, interpretation, and reporting of experimental results.
• Contribute to the generation of regulatory submission documents.
• Stay abreast of the latest scientific literature and emerging technologies in oncology.
• Present research findings at internal meetings and external scientific conferences.
• Manage external collaborations and contract research organizations.
• Ensure compliance with all laboratory safety regulations and company policies.
• Foster a collaborative and innovative research environment.

Qualifications:

• Ph.D. in Molecular Biology, Cell Biology, Pharmacology, or a related field.
• Minimum of 5 years of post-doctoral or industry research experience in oncology drug discovery.
• Proven track record of successfully leading research projects from concept to preclinical stages.
• Extensive experience with various in vitro and in vivo oncology models and assay development.
• Strong understanding of cancer biology, signal transduction pathways, and modern therapeutic modalities.
• Excellent written and oral communication skills, with a demonstrated ability to present complex scientific data.
• Proficiency in data analysis software (e.g., GraphPad Prism, R).
• Experience with immunotherapy and small molecule drug development is highly desirable.
• Ability to work effectively in a fast-paced, team-oriented environment.
• Strong problem-solving and critical-thinking abilities.

This is an exceptional opportunity to make a significant impact in the fight against cancer. Join a team dedicated to advancing life-saving therapies and contribute to cutting-edge pharmaceutical innovation.

Our client is a global leader in pharmaceutical innovation, and they are seeking an exceptional Senior Data Scientist to join their fully remote research and development team. This is a unique opportunity to contribute to critical drug development projects from the comfort of your home office. You will leverage your expertise in statistical modeling, machine learning, and data analytics to extract valuable insights from complex biological and clinical datasets, accelerating the path to new therapies. This remote-first position requires a high degree of self-discipline, proactive communication, and the ability to collaborate effectively with a distributed team across various time zones.

Key Responsibilities:

• Develop and implement advanced statistical and machine learning models to analyze large-scale R&D data, including genomics, proteomics, clinical trial data, and real-world evidence.
• Design data-driven strategies to support drug discovery, preclinical development, and clinical trial design and analysis.
• Identify opportunities to apply AI/ML techniques to solve challenging problems in drug development, such as patient stratification, biomarker discovery, and predictive modeling of drug efficacy and safety.
• Collaborate with computational biologists, statisticians, and clinical scientists to define data requirements, interpret results, and translate findings into actionable insights.
• Create compelling data visualizations and dashboards to communicate complex findings to diverse audiences, including senior management and scientific teams.
• Contribute to the development and maintenance of data infrastructure and best practices for data governance and reproducibility.
• Stay abreast of the latest advancements in data science, machine learning, and their applications in the pharmaceutical industry.
• Mentor junior data scientists and contribute to the growth of the data science community within the organization.
• Proactively engage in virtual team meetings and knowledge-sharing platforms to ensure seamless collaboration.

Qualifications:

• Master's or Ph.D. in Data Science, Statistics, Computer Science, Bioinformatics, or a related quantitative field.
• Minimum of 7 years of experience in data science, with a significant portion focused on the pharmaceutical or biotechnology industry.
• Proficiency in programming languages such as Python or R and associated data science libraries (e.g., scikit-learn, TensorFlow, PyTorch, pandas).
• Extensive experience with various statistical modeling and machine learning techniques (e.g., regression, classification, clustering, deep learning, survival analysis).
• Experience handling and analyzing diverse biological datasets (e.g., genomics, transcriptomics, proteomics, clinical data).
• Familiarity with cloud computing platforms (AWS, Azure, GCP) and big data technologies.
• Excellent communication and presentation skills, with the ability to explain technical concepts to non-technical stakeholders.
• Proven ability to work independently, manage projects effectively, and thrive in a remote work environment.
• Strong problem-solving skills and a passion for applying data to solve complex scientific challenges.

This role offers the flexibility of a fully remote setup, enabling you to contribute to life-changing pharmaceutical research regardless of your physical location.

Our client, a prominent pharmaceutical company at the forefront of life-saving therapeutics, is looking for a Principal Research Scientist to lead groundbreaking research in oncology drug development, based in Washington, D.C., US . This senior role will be instrumental in identifying and validating novel drug targets, designing and executing preclinical studies, and contributing to the strategic direction of our cancer research pipeline. You will leverage your extensive expertise in molecular biology, cell signaling, and pharmacodynamics to drive innovation and accelerate the discovery of new cancer treatments. Responsibilities include leading a team of dedicated scientists, mentoring junior researchers, developing robust assay systems, and interpreting complex experimental data. You will also play a key role in intellectual property generation, manuscript preparation, and presentation of research findings at scientific conferences. Collaboration with internal cross-functional teams, including medicinal chemistry, pharmacology, and clinical development, is essential. The ideal candidate will possess a proven track record of independent research and publication in top-tier peer-reviewed journals. A strong understanding of cancer biology, common oncogenic pathways, and emerging therapeutic modalities is required. Experience with biologics, small molecules, or combination therapies in oncology is highly desirable. This position offers a unique opportunity to contribute to the development of next-generation cancer therapies and make a profound difference in the lives of patients worldwide. The hybrid work model allows for flexibility while maintaining close collaboration with R&D teams.

Join our global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes to our patients. We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates itwhere your skills and values drive our collective progress and impact.
We are seeking a highly experienced and strategic Director/Senior Director of Project Management to lead a cross-functional pharmaceutical program from mid to late-stage development. This individual will play a critical role in driving program execution, identifying and mitigating risks, ensuring delivery of key milestones and ensuring alignment with corporate objectives. The ideal candidate will bring minimum of 10 years of experience in pharmaceutical R&D project management, with a proven track record of success in managing complex development programs. Experience in hepatology, immunology, or gastroenterology is a plus but not required.
Responsibilities:
+ Drives strategic execution of cross-functional drug development programs, ensuring seamless progression from mid-stage development through successful regulatory approval and market launch
+ Partners with executive and C-suite leadership across Development, Regulatory, Clinical, Commercial, Medical, and Manufacturing to align program execution with high-level corporate strategy and long-term portfolio objectives
+ Leads senior cross-functional teams alongside the Program Head, setting program vision, establishing priorities, and making key decisions to drive business impact and portfolio growth
+ Champions the creation and maintenance of robust, integrated project plans, long-range timelines, budgets, and enterprise-level risk mitigation strategies, anticipating industry trends and regulatory shifts
+ Directs and orchestrates program governance forums, senior leadership meetings, scenario planning, and strategic decision-making processes, ensuring issues are escalated to the highest organizational levels and resolved with minimal risk to the business
+ Mentors and develops future leaders by providing strategic guidance and oversight to project managers and cross-functional team members, fostering a culture of accountability, innovation, and excellence
+ Ensures unwavering compliance with global regulatory requirements and internal quality standards, proactively identifying emerging challenges and navigating complex environments
+ Leads continuous improvement initiatives for project management processes, tools, and methodologies, setting benchmarks for operational excellence and driving transformational change across the organization
Qualifications:
+ Bachelors degree required. Life sciences, pharmacy, engineering discipline preferred; advanced degree (PhD, PharmD, MBA) preferred
+ Minimum 10 years of progressive experience in pharmaceutical project or program management, with a proven track record of managing assets across all phases of development
+ Strong understanding of drug development processes, regulatory and commercialization strategies
+ Experience in hepatology, gastroenterology, or immunology therapeutic areas or with medical devices is a plus but not required
+ Demonstrated ability to lead cross-functional teams in a matrixed environment
+ Excellent communication, leadership, and stakeholder management skills
+ PMP or equivalent certification preferred
+ Strategic thinking with the ability to translate vision into actionable plans
+ Experience working in global teams, regulatory agencies and managing external partners or CROs
+ Strong financial acumen and experience managing program budgets
+ Ability to influence and lead in a matrixed environment
+ Comfortable navigating ambiguity and driving clarity
+ Strong business acumen and understanding of the drug development lifecycle
+ Proficiency in project management tools (e.g., MS Project, Smartsheet, OnePlan)
The range of starting base pay for this role is 175K 241K. Actual starting pay will be based on a wide range of factors including, but not limited to, relevant skills, experience, qualifications, education and location. In addition to base pay, this position is eligible for participation in either (i) our annual bonus program or (ii) a sales incentive plan.
Benefits package includes a comprehensive Medical (includes Prescription Drug), Dental, Vision, , Flexible Spending Accounts, 401(k) with matching company contribution, discretionary time off, paid sick time, tuition reimbursement, parental leave, short-term and long-term disability, life insurance, accidental death & dismemberment insurance, paid holidays, employee referral bonuses and employee discounts.
#LI-Hybrid
We are an Equal Opportunity Employer. EOE Disability/Veteran. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates collaboration.