47 benefits coding jobs found

Biogen About This Role As a Clinical Trial Management PV Lead, you will play a pivotal role in ensuring the operational excellence and strategic oversight of safety processes, contents and data quality within clinical studies. Positioned within our pharmacovigilance team, this role is integral to maintaining compliance with global safety regulations while driving innovation in safety data review and management practices. From utilizing tools and processes for safety database configurations to leading quality reviews of Individual Case Safety Reports (ICSRs), you will be instrumental in shaping our clinical safety initiatives. Your expertise will support cross-functional collaborations, enhance safety data quality, and contribute to regulatory filings and ongoing safety surveillance and risk management activities. As a senior leader in the team, you will identify areas for improvement within the pharmacovigilance system, lead strategic initiatives, and contribute to the...

Biogen This is a remote-based position, candidate must be located within the USA About This Role The Principal Medical Writer serves as a scientific communication and innovation leader within Biogen's Medical Writing department, focusing on leveraging Generative AI (GenAI) technologies to transform regulatory writing. In this role, you will combine your expertise in regulatory document strategy with forward-looking approaches to content generation, automation, and AI-enabled writing support. You will author and oversee preparation of high-quality clinical regulatory documents (e.g., clinical summaries, CTAs, INDs, and briefing packages) and collaborate closely with cross-functional teams to ensure clarity, accuracy, and consistency. Additionally, you will work on collaborative initiatives with internal and external partners to develop and pilot GenAI tools that enhance efficiency, quality, and compliance in medical writing workflows. Coding experience is not required, but...

Biogen About the Role: This application is for a 6-month student role from July - December 2026. Resume review begins in February 2026. The Immunology Research Unit is focused on the development of therapies for patients suffering from autoimmune diseases. This position offers an opportunity to work with experienced drug discovery scientists as part of a collaborative cross-functional team. The co-op will gain experience in designing and executing hands-on experiments to answer key scientific questions to advance a research program. What You'll Do: As a co-op, you will work side-by-side with experienced scientists to learn and become independent in primary human peripheral blood mononuclear cell (PBMC) in vitro assays. Using your training, you will address key biology questions aimed at understanding innate immune cell function, its contribution to autoimmunity, and opportunities for modulation of critical pathways. This will include assisting the biology team in...

Biogen About This Role The Senior Manager, Medicaid Operations, serves as a key leader within the Medicaid Operations team, responsible for guiding critical operational, analytical, and compliance-focused activities to safeguard against revenue leakage. This role partners closely with cross-functional teams-including Legal, Government Pricing, Trade, and Reimbursement-as well as external stakeholders to identify, investigate, and resolve 340B duplicate discount issues. The Senior Manager will define and drive operational excellence to ensure full compliance with federal and state Medicaid program requirements. The ideal candidate brings strong Medicaid Rebate operations expertise, in-depth knowledge of the 340b program, and a proven ability to lead operational processes. This role requires exceptional problemsolving skills, sound judgment, and the ability to lead teams through complex and evolving regulatory environments. What You'll Do 340B Duplicate Discount...

Nuvalent, Inc. The Company: With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role: Reporting to the Senior Director, Payer & Reimbursement, the Associate Director, Pricing & Contracting Operations plays a critical role in shaping and executing the company's pricing and contracting strategies to optimize access to Nuvalent's product portfolio, as well as playing a key part in driving pricing and contracting strategy and management. We are a growing pharmaceutical company with a commitment to delivering innovative, oral targeted therapies for oncology patients. We are seeking a dynamic and strategic professional to lead pricing and contracting operations....

Biogen TBD Job Level: Internship Additional Information The base compensation range for this role is: $23.00-$29.00 The actual hourly wage offered will consider the candidate's current academic level and degree candidacy, inclusive of Associate, Bachelor's, Master's, JD, MD, PhD and MBA programs. It will comply with state or local minimum wage requirements specific to the job location. In addition to compensation, Biogen offers a range of benefits designed to support our educational employees, including, but not limited to: Company paid holidays Commuter benefits Employee Resource Groups participation 80 hours of sick time per calendar year Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the...

Biogen About the Role: This application is for a 12-week internship role from June - August 2026. Resume review begins in January 2026. Biogen's Drug Metabolism and Pharmacokinetics (DMPK) department is seeking a highly motivated and talented intern with excellent knowledge and experience in LC-MS/MS to join our bioanalytical group. As a summer intern within the bioanalytical group, you will explore various technologies to further expand our understanding and capabilities for quantitative bioanalysis of oligonucleotides. What You'll Do: As an intern, you will actively contribute to the development of novel bioanalytical methods, including the pioneering of novel techniques for quantification of oligonucleotides across various biological matrices such as plasma, CSF, and tissue. You will work on research projects with training and guidance from mentors and experienced co-workers. Your role will involve managing projects, from the initial evaluation of new...

Biogen About This Role The Associate Director, Data Management within US Decision Sciences / Data & Analytics provides strategic and executional leadership across commercial data domains, ensuring the consistent delivery of high-quality, analytics-ready data to support insights, reporting, and field execution at scale. The Associate Director owns complex, cross-domain data initiatives, sets standards and best practices for data management, and serves as a primary thought partner to Analytics, Reporting, Field Operations, IT, and senior stakeholders. The role goes beyond execution to shape the data management roadmap for 1-2 brands, proactively address systemic data challenges, and drive continuous improvement across platforms, vendors, and processes. What You'll Do Own strategy and execution for multiple commercial data domains, ensuring reliable, analytics-ready data delivery. Lead complex, cross-functional data initiatives that span analytics, reporting,...

Biogen About the Role: This application is for a 12-week internship role from June - August 2026. Resume review begins in February 2026. Biogen's Health Equity & Clinical Innovation team is seeking a temporary intern to support the integration of health equity into core medical affairs operating processes and capabilities. This role will focus on assessing if/how equity considerations are currently applied and where they are missing or inconsistently addressed across medical affairs teams, strategy, evidence generation, scientific education, and engagements. In addition to process assessment, the intern will help translate health equity principles into practical medical affairs education resources that can be used by disease teams. The role is designed to generate scalable, repeatable impact by embedding equity into how medical affairs works-not as a standalone initiative, but as a core capability. This role will help us design and integrate community education as a...

Biogen About the Role: This application is for a 12-week internship role from June - August 2026. Resume review begins in February 2026. Biogen's Health Equity & Clinical Innovation team is seeking a motivated intern to support health equity driven medical affairs initiatives focused on rural communities. This internship will provide hands-on exposure to how medical affairs integrates health equity principles into disease understanding, evidence generation, scientific education, and external stakeholder/community engagement. The intern will examine how geography, culture, infrastructure, and trust influence diagnosis, treatment access, clinical research participation, and real-world outcomes in rural settings. Insights generated through this role will directly inform medical affairs strategy, including disease area strategic planning, medical education priorities, feasibility assessments for late-stage development and post-approval studies, and long-term health...

Biogen About the Role: This application is for a 6-month student role from July - December 2026. Resume review begins in February 2026. Biogen's Health Equity & Clinical Innovation team is launching a medical affairs focused co-op to examine how Gen Z health behaviors, trust dynamics, and digital ecosystems should inform the future of disease strategy, evidence generation, and scientific engagement. This role will evaluate how Gen Z defines health and illness, seeks medical information, evaluates scientific credibility, and engages with healthcare systems and clinical research. Particular emphasis will be placed on the impact of social media, AI-enabled tools, online communities, and digital misinformation on scientific trust, benefit-risk understanding, and participation in care and research. Insights generated through this co-op will directly inform medical affairs strategy and Development 2030 planning, including disease-level planning, feasibility...

Biogen About This Role: Biogen is seeking a motivated and passionate individual to join our team as a Director, Pathology. This role is integral to our mission of delivering transformative and safe drugs to patients by providing veterinary toxicologic pathology expertise across our diverse portfolio. You will be responsible for supporting the advancement of our pipeline by designing, executing, and interpreting toxicology studies, assessing safety risks, and contributing to project strategy across all phases of Drug Discovery and Development, as well as for marketed products. As part of an established team within the Nonclinical Safety function, you will collaborate closely with Toxicology and Study Management functions. In this high-impact position, you will play a pivotal role in enabling the delivery of first-in-class treatments and therapies that improve patient outcomes. What You'll Do: Provide pathology expertise to the design and conduct of GLP and non-GLP...

Biogen About the Role: This application is for a 6-month student role from July - December 2026. Resume review begins in January 2026. You will be an integral member of the Global Media Relations and External Communications team, helping to manage the company's reputation with journalists and top media outlets, global product and pipeline communications, and analyzing public perception and sentiment about the company. In total, you will be part of a 5-person team that sits within the broader 30+ person Global Corporate Affairs department. The department is responsible for positioning Biogen as a leader in innovative science and enhancing the company's reputation with key stakeholders, employees, and patients. As part of this department, you will help support the company's business objectives by communicating and informing Biogen's company value proposition and bringing the brand's promise to life. What You'll Do: As a co-op, you will: Support corporate communication...

Nuvalent, Inc. The Company: With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role: Reporting to the Director, Patient Access Services, the Associate Director, Access & Reimbursement (ADAR) will be a critical member of the Market Access team to create patient impact by providing field access support and education to healthcare professionals (HCPs), helping to maximize patient access to products. This role will be an empowered and confident subject matter expert in supporting complex patient cases through understanding the payer landscape, customer engagement, and internal cross-functional collaboration. This role will support the patient access strategy and...

Biogen About This Role As the Associate Scientific Director, ClinicalPharmacology you will serve as the clinicalpharmacologylead on program and study teams, providing strategic leadership in the development and execution of clinicalpharmacologyplans for drug candidates. You will integrate knowledge of clinical and quantitativepharmacologyto optimize and provide rationale for doses, dosage regimens, and study designs throughout the drug development lifecycle. What You'll Do Provide clinicalpharmacologyexpertise to program and study teams throughout a molecule's lifecycle (discovery through development) Provide functional representation on development program and study teams Develop & implement the clinicalpharmacologydevelopment plan, considering all aspects (strategic, scientific, translational, and clinical) Define key milestones and decisions within the clinicalpharmacologydevelopment plan and identify risks and mitigation strategies Lead execution of...

Biogen About This Role The Associate Director, Nephrology Payer Insights is responsible for the successful scope, execution and delivery of all payer reporting, analytics, research, and insights to support the Nephrology business unit by working with internal colleagues within Market Access & Reimbursement (MA&R) and other cross-functional partners and stakeholders, including brand, field teams, commercial operations and insights, finance, and global. You will develop and execute on an insights plan to support successful launches in the nephrology space. This includes developing an understanding of the payer landscape for nephrology, assessing payer views on price/value and unmet needs in nephrology, understanding the providers in this space, including practice economics, and assessing the patient access landscape, including patient affordability. You will develop and maintain suite of standard reporting within MA&R at the national and local level, including...

Biogen About This Role The Neuromuscular Development Unit at Biogen is accountable for developing ground-breaking therapies in Spinal Muscular Atrophy (SMA), Amyotrophic Lateral Sclerosis (ALS), and muscle diseases from early to late-stage clinical development. As a member of the team, the associate medical director will work on late-stage SMA drug and device programs and potentially contribute to other programs and/or develop our platform capabilities. This role will drive the progression of a deep clinical portfolio and assist the team in achieving innovative clinical trial designs, biomarkers, clinical endpoints, and regulatory interactions. What You'll Do Maintain accountability for clinical trial design, execution, and interpretation of clinical trial results for late-stage SMA drug and device programs. Support the development and oversight of study protocols and amendments, clinical study reports, training documents, and other clinical and regulatory documents....

Biogen About the Role: This application is for a 6-month student role from July - December 2026. Resume review begins in January 2026. As a Co-op in Parenteral Drug Product Development, you will be an integral part of the team focused on the study and testing of various oligonucleotides across diverse formulations and steam sterilization conditions. This role offers hands-on experience in formulation science and sterilization techniques, providing an invaluable learning opportunity that enriches your resume. You will contribute to internal reports as a co-author, enhancing your research and writing skills. This position allows you to immerse yourself in departmental meetings, gaining a comprehensive understanding of oligonucleotide drug product development within the pharmaceutical industry. Additionally, you will present your research findings in both oral and written formats, further developing your communication skills. Collaborating closely with a pharmaceutical...

Biogen About This Role: As the Associate Director of Integrated Insights & Analytics, you will take on a pivotal individual contributor role within the US Decision Sciences team. Collaborating closely with the US Brand team, you will be the driving force behind generating actionable customer and market insights for a single inline or pipeline asset across various indications. Your role will be to own and develop the integrated insights narrative, synthesizing primary research and secondary data to create executive-ready storytelling that significantly influences brand and launch decisions. This position is vital to bridging the gap between data and strategic decision-making, ensuring that insights translate into impactful business outcomes. By working collaboratively across functions, you will ensure that insights are seamlessly integrated into broader business strategies. What You'll Do: Serve as the go-to insights partner for the asset, aligning work to brand...

Biogen About This Role The Senior Manager, Standards & Governance is part of the Global Medical Capabilities Team, a strategic partner within Global Medical Affairs. This role will be responsible for supporting governance and implementation of global business processes in close partnership with Compliance and Global Medical leadership. The role serves as a key resource for the continued process and tool redesigns for all Global Medical owned activities and works through business partnership, data analytics, monitoring, training, and communications. What You will Do Provide consulting support to Global Medical business on the appropriate application of all Biogen policies and requirements. Participate in implementation of business processes and systems supporting release of new and/or updated Policy, SOP, and other written guidance owned by Global Medical and/or Corporate Compliance Identify, and help implement new, or changes to, processes required due to...