928 jobs found in Princeton, NJ

Associate Director, Us Gu, Global Medical Oncology 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. Position reports to the Senior Director, US GU Tumors Portfolio of Global Medical...

Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology. Here at Ascendis, we pride ourselves on exceptional science, visionary leadership, and skilled and passionate colleagues. Guided by our core values of Patients, Science, and Passion, we use our TransCon drug development platform to fulfil our mission of developing new and potentially best-in-class therapies to address unmet medical needs. Our culture fosters a place where skilled, adaptable, and highly resourceful professionals can truly make their mark. We offer a dynamic workplace for employees to grow and develop their skills. We are looking for an Associate Director, US Medical Training, who will work within the US Medical Affairs team at Ascendis Pharma. This crucial role will be supporting scientific training across various teams in the US Business Unit. This is...

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. Read more: careers.bms.com/working-with-us . Position Summary: Position reports to the Senior Director, US GU...

Ascendis Pharma is a fast-growing global biopharmaceutical company committed to transforming the lives of patients with rare diseases and delivering innovative therapies through our proprietary TransCon® technology platform. We are actively seeking an experienced Associate Director, US Medical Training who will take the lead in developing and implementing comprehensive training programs for our Medical Affairs team and other cross-functional stakeholders. You will ensure our teams are equipped with the knowledge and skills necessary to effectively communicate scientific data and product information. This role is crucial to ensuring our teams maintain high standards of medical education and compliance within the rapidly evolving landscape of the pharmaceutical industry. Position Summary The Associate Director, US Medical Training will develop and deliver training programs that not only educate our staff but also enhance the overall effectiveness of our Medical Affairs...

A biopharmaceutical company in Princeton is seeking an Associate Director, US Medical Training to develop training strategies supporting scientific acumen across the US Medical Affairs team. This role involves collaboration with various teams, delivering training materials, and ensuring compliance with corporate policies. Candidates should have an advanced degree and extensive experience in medical affairs, ideally in endocrinology. Benefits include a competitive salary and comprehensive perks. #J-18808-Ljbffr

Associate Director, Medical Scientist (Project Management) Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers. Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission. Taiho's success is founded on ensuring we always act with accountability, collaboration, and trust. By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are working on cutting‑edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients. Advanced technology, a world‑class clinical development organization, and state‑of‑the‑art facilities: these and other resources empower us to innovate and touch the lives of more and more...

Medical Coder job at Claims Theory. New York, NY. Job Description Certified Professional Coder / Bill Review Expert Responsibilities: Review medical bills related to MVA injuries sustained for NJ and or NY covered insureds Conduct reviews of medical bills and supporting documentation to ensure proper codes assigned Assign proper codes as needed based on review outcome Use various resources, IE: eBooks, 3M software to support reviews Interpret fee schedule guidelines and apply those guidelines in daily reviews Document review outcomes for customer in a professional easy to understand manner Participate in conference calls as needed with customer and/or attorneys Assist with various special projects and other duties as assigned Qualifications and Experience: 3-5 years of medical billing experience specifically NJ / NY PIP fee schedules Strong communicate skills, must be able to explain outcome of review, both written and verbally Extensive knowledge of coding...

Description The US Associate Director, Medical Affairs Northeast will serve as a liaison to the medical/scientific community and will be responsible for establishing, developing, and maintaining relationships with prominent experts in pediatric neurology and in epilepsy within the geographic area of coverage. This position reports to the Medical Director, Orphan Drug Division. RESPONSIBILITIES: Build, maintain, and manage professional relationships with Key External Experts (KEEs) to organize networks at state levels within their designated region Ensure the appropriate dissemination of clinical and scientific information regarding marketed and pipeline compounds in a timely, ethical and health care provider (HCP)-focused manner Implement clinical and educational strategies in collaboration with other company colleagues for designated HCPs/KEEs. This includes organizing medical and scientific training sessions, conferences and symposiums in medical centers and...

Job Description About Us Welcome to ANI Pharmaceuticals, where we are dedicated to improving and enhancing patients' lives through the manufacturing and distribution of high-quality pharmaceutical products. With a diverse portfolio of generic and branded pharmaceuticals, ANI is a trusted partner for healthcare providers, pharmacists, and patients alike. We understand the importance of accessibility, and our products are available across a wide range of therapeutic areas, contributing to the well-being of communities globally. About the Role The Medical Science Liaison (MSL) will serve as a liaison to the medical/scientific community and will be responsible for establishing, developing, and maintaining relationships with medical experts in Nephrology nationwide. The MSL is a credentialed therapeutic and disease expert that engages in scientific exchange with leaders in both the external medical and scientific communities. MSLs are responsible for conducting...

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions to meet the needs of our patients, care partners, families and employees. Our people are compassionate, candid, and purposeful, and our business is innovative and rooted in science. We believe that being proudly authentic and determined to be our best is essential to fulfilling our purpose. Yes, our work is incredibly serious and impactful, but we have big ambitions, bring a ton of care to pursuing them, and have a lot of fun while doing so. Does this inspire you and feel like a fit? Then we would love to have you join us! The Role The Associate Director of Medical Communications will be...

Hybrid Employee Value Proposition: Exciting Opportunity in Medical Affairs! Join a dynamic mid-size pharmaceutical company dedicated to improving the lives of patients with hematological and oncological conditions. In this role, you’ll collaborate closely with the therapeutic area lead and gain exposure to diverse matrix teams, senior leadership, and external stakeholders. Our organization combines the agility of a moderate-sized company with the influence of a significant industry footprint. You’ll learn from innovative minds while making a meaningful impact, your contributions will truly stand out. Position Summary: The Associate Director (AD) Medical Scientist, collaborating with the Therapeutic Area (TA) Medical Director, supports the development and execution of Medical Affairs strategies to advance Taiho Oncology’s products in US and international markets by ensuring accurate scientific communication, compliance, and alignment with business objectives. The role involves...

A leading pharmaceutical company in Princeton, NJ, is seeking an Associate Director, Medical Scientist. This role focuses on advancing oncology products through strategic collaboration and scientific communication, requiring at least 5 years of experience in Medical Affairs. The position offers a hybrid work model and competitive compensation ranging from $208,250 to $245,000, with benefits including bonuses and a 401(k). Join us in our mission to improve patient outcomes in oncology. #J-18808-Ljbffr

**About Otsuka**We defy limitation, so that others can too. In going above and beyond—under any circumstances—for patients, families, providers, and for each other. It’s this deep-rooted dedication that drives us to uncover answers to complex, underserved medical needs, so that patients can push past the limitations of their disease and achieve more than they thought was possible each day.**About the Role**The Omnichannel Center of Excellence is dedicated to driving innovation, building, and delivering capabilities that enhance Otsuka’s opportunity to make an impact in the lives of those we serve. We achieve this through our relentless focus on customer centricity, patient empathy, expertise in enabling pathways for disease education and awareness of management options, and our unwavering commitment to supporting access to treatment.We are looking for an **Omnichannel Data Scientist**, **Medical Omnichannel** with strong expertise in artificial intelligence, encompassing machine...

Associate Director, Market Access And Payer Relations Abbott is seeking a passionate and driven professional to join our team as Associate Director, Market Access and Payer Relations, supporting the East Coast region of the United States. This strategic role is focused on securing and maintaining market access for Abbott's innovative cardiovascular and neuromodulation (CV&N) technologies through proactive engagement with U.S. private Payers and affiliated entities. What You'll Work On Strategic Payer Engagement: Build and sustain relationships with key decision-makers at national and regional commercial health plans to educate stakeholders, influence medical policy development, and expand patient access to Abbott's cardiovascular and neuromodulation technologies. Market Access Strategy: Design and implement robust strategies to secure and advance coverage for both existing and emerging CV&N products, aligning with broader business objectives. Cross-Functional...

Overview The Associate Director, Portfolio Delivery Lead, in Global Medical Oncology (GMO), plays a critical role in executing initiatives in the Medical Oncology portfolio-wide strategic plan. The Portfolio Delivery Lead will ensure integration of asset objectives and activities into oncology and hematology disease area strategic plans and implementation with key matrix stakeholders. The role will report to the Senior Director, Portfolio Strategy Lead, Global Medical Oncology. Key Responsibilities Lead the execution of initiatives such as Advisory Boards, thought leader interactions, and congress encounters to collect insights and support shaping a portfolio-wide strategic plan for Medical Oncology. Collaborate with congress excellence team to align portfolio-wide congress booth strategy. Align with Medical Product Leads, Medical Communications, and Medical Societies Leads for oncology and hematology disease area portfolio-wide congress strategy. Develop and implement...

Supervisor, Automated Medical Operations Changing lives. Building careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care. The Supervisor, Automated Medical Operations is responsible for the medical dispersion production activities for CMC (Collagen Manufacturing Center) to ensure the safety, efficacy, and quality of our medical devices. This includes assigning and monitoring daily 2nd shift activities of production staff and partnering with other support departments to efficiently and compliantly complete work and work processes as per outlined production schedules. All production is to be conducted in compliance with ISO 7 Clean Rooms and with Good Manufacturing Practices (GMP),...

A leading medical device manufacturer in Plainsboro Township is seeking a Supervisor for Automated Medical Operations. This role involves supervising cleanroom operators, ensuring compliance with FDA regulations, and fostering a Lean work culture. Ideal candidates should hold a Bachelor’s degree in a relevant field with at least 3 years of leadership experience in a GMP regulated industry. Strong communication skills and experience in batch manufacturing are essential. Competitive salary range is offered, along with a comprehensive benefits package. #J-18808-Ljbffr

Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care. The Supervisor, Automated Medical Operations is responsible for the medical dispersion production activities for CMC (Collagen Manufacturing Center) to ensure the safety, efficacy, and quality of our medical devices. This includes assigning and monitoring daily 2nd shift activities of production staff and partnering with other support departments to efficiently and compliantly complete work and work processes as per outlined production schedules. All production is to be conducted in compliance with ISO 7 Clean Rooms and with Good Manufacturing Practices (GMP), Quality Systems Regulations, Standard...

A hearing healthcare leader in Franklin Township seeks a Manager of Medical Billing to oversee billing submissions and collection activities. The ideal candidate will have a Bachelor’s Degree and 5+ years of experience in billing within a high-volume environment. Responsibilities include managing teams, ensuring accurate claims submissions, and liaising with various departments. The position offers a salary target of $115k - $125k. Join a dynamic team committed to making a difference in hearing health. #J-18808-Ljbffr

Medix - American Metro Center 300 [Medical Records Clerk] As a Coder at Medix, you'll: Analyze medical records to assign appropriate codes for billing and insurance purposes; Ensure accuracy and compliance with coding guidelines and regulations; Collaborate with healthcare professionals to clarify diagnoses and procedures; Maintain confidentiality of patient information; Update coding knowledge through continuous education and training; Assist in audits and reviews to improve coding processes and accuracy...Hiring Immediately >>

Become a part of our caring community and help us put health first The Medical Coding Auditor reviews medical claims submitted against medical records provided, to ensure correct coding guidelines are met (e.g., ICD-10-CM, CPT, HCPCS). The Medical Coding Auditor's work assignments are varied and frequently require interpretation and independent determination of the appropriate courses of action. The Medical Coding Auditor contributes to overall cost reduction, by increasing the accuracy of provider contract payments in our payer systems, and by ensuring correct claims payment for appropriate CPT/ HCPCS code assignments. Analyzes, enters and manipulates database. Responds to or clarifies internal requests for medical information. Understands department, segment, and organizational strategy and operating objectives, including their linkages to related areas. Makes decisions regarding own work methods, occasionally in ambiguous situations, and requires minimal direction and...

Medical Coding Specialist Review, analyze, and code medical record documentation to include, but not limited to, medical, diagnostic and procedural information for the correct ICD-9 and/or ICD-10 and/or CPT-4 HCPCS codes to the greatest specificity. Abstracts demographic and coding information into the information system accurately and completely. Reviews documentation for medical necessity. Audits orders and claims before submission for entirety and accuracy and to minimize claim denials. Assesses records and prepares reports. Develops effective working relationships with physicians and other stakeholders. Project Details: Evaluate medical record documentation and charge ticket coding to optimize reimbursement by ensuring that diagnostic and procedural codes and other documentation accurately reflect and support the visit Compile necessary documentation prior to coding review; when documentation is not available, performs the appropriate steps to obtain the necessary...

A leading health insurance company is seeking a qualified Inpatient Medical Coding Auditor to work fully remote in New Jersey. Responsibilities include reviewing inpatient claims for accuracy, ensuring correct payments, and working independently. Candidates should possess an RHIA, RHIT, or CCS certification, along with MS-DRG coding experience. The role offers competitive pay ranging from $71,100 to $97,800 annually, and occasional travel may be required for training and meetings. #J-18808-Ljbffr

Become a part of our caring community and help us put health first The Inpatient Medical Coding Auditor extracts clinical information from a variety of medical records and assigns appropriate procedural terminology and medical codes (e.g., ICD-10-CM, CPT) to patient records. The Inpatient Medical Coding Auditor work assignments involve moderately complex to complex issues where the analysis of situations or data requires an in-depth evaluation of variable factors. Humana is looking for an experienced medical coding auditor to review inpatient hospital claims for proper reimbursement, handle provider disputes in a result-oriented and metrics-driven environment. If you are looking to work from home, for a Fortune 100 company that focuses on the well-being of their consumers and staff, and rewards performance, then you should strongly consider the Inpatient Coding Auditor (MSDRG). The Inpatient Medical Coding Auditor contributes to overall cost reduction, by increasing the accuracy...