CrawlJobs Logo

Executive Director, Medicine Development Leader

us.gsk.com Logo

GSK

Location Icon

Location:
United States; United Kingdom , Waltham ▼

Category Icon
Category:
Research and Development

Job Type Icon

Contract Type:
Not provided

Salary Icon

Salary:

242250.00 - 403750.00 USD / Year
Save Job
Save Icon
Job offer has expired

Job Description:

GSK is seeking a highly skilled Executive Director, Medicine Development Leader (MDL), to strategically lead the optimal global development of a renal medicine at an asset level, acting as the single point of accountability for the medicine from clinical Proof of Concept (PoC) to Approval in the first major market(s). By working with the various stakeholders across GSK’s Medicine Development matrix (R&D, Manufacturing, Commercial, etc.), you will define the strategic vision and operational plan for the medicine, aligning it with the overall organizational strategy. You will create and lead the matrixed Medicine Development Team (MDT), which is responsible for representing the various disciplines required to optimally deliver the development of the medicine including Clinical Development, Medical, Commercial and Manufacturing, amongst others. The Executive Director, MDL reports to the SVP & Head Advanced Pipeline Unit- Respiratory, Immunology and Inflammation Research Unit.

Job Responsibility:

  • Act as a single point of accountability in GSK for all aspects of a medicine being developed globally, from proof of clinical activity (POC) to Approval in all major market(s)
  • Work closely with the Early Development Lead (EDL) and Medicine Commercial Lead (MCL) to ensure a smooth transition of the lead indication(s) from the EDL upon achievement of clinical PoC and to the MCL upon Approval in first major market(s)
  • Post-approval, provide key support to the Medicine Commercial Team (MCT) in the first major markets ensuring the MDT provides optimal support to registration, including Post-Marketing Requirements (PMRs) and life cycle management (LCM) in the major markets
  • Work with the functional line Heads supporting RIIRU to select MDT members and lead this multi-disciplinary matrix team, supporting differentiated development for team members, owning the performance of the MDT and partnering with Line Managers to drive performance
  • Partner with the Pipeline Project Manager (PPM), energize and motivate the MDT to drive a high performing team and operational delivery of the project, including setting team objectives to ensure successful project delivery, including options for acceleration, parallel indication development and smart risk-taking.
  • Partner with R&D Business Development, leading the development planning for a prospective in-licensed asset by bringing together input from the relevant functions and TA experts to develop a Medicine Profile (MP) and development plans including but not limited to clinical feasibility, regulatory planning and CMC risk mitigation
  • Leads the cross-functional MDT to: Establish a compelling vision for the medicine and Target Medicine Profile (TMP) which positions the medicine within the R&D strategy taking the competitive landscape into account, translating GSK’s strategy into asset strategy and actionable plans for multiple areas or functions
  • Deliver differentiated medicines of value for patients, stakeholders and markets through an evidence package that supports regulatory approval, market access and the product’s life cycle
  • Prioritize and maximize the asset’s development options including developing multiple indications
  • Partner with the Global Medical Lead (GML) and MCL to develop an indication expansion and LCM plan for the asset.
  • Make clear evidence-based go / no go / accelerate decisions and identify clear inflection points, based on results
  • Ensure excellence in execution of all governance processes, including MDT members, on oversight of clinical studies, patient safety & pharmacovigilance, scientific engagement and promotional practices
  • Enhance patient focus by incorporating the voice of the patient into development plans
  • Increase visibility amongst the external communities to bring medical solutions to patients with unmet medical needs
  • Embed core processes including cost efficiency, adoption of new technology, risk identification & management, compliance with policy
  • Promote organizational reputation and drives asset value by engaging and negotiating with internal and external stakeholders
  • Ensures quality & compliance oversight in line with R&D expectations and project needs
  • ensures quality of data and science
  • Serves as the asset’s single point of contact and spokesperson to Senior Management, senior boards, other relevant internal governance committees and external Advisory Committees, as needed
  • Delivers and manages the asset resourcing plan (people & finances), including serving as the single point for accountability for managing the asset budget to the agreed variance, working closely with the PPM and Finance Partner to do so

Requirements:

  • Advanced degree including MD, PhD, PharmD, MBA, MS
  • Drug development expertise in the global pharmaceutical/biotechnology industry
  • Filing experience with BLA/NDA/MAA submissions as a core responsibility
  • Experience in the entirety of drug development across the R&D/commercial life cycle including Discovery, late-stage Development, Regulatory, Manufacturing Medical and Commercial
  • Experience in product development and/or commercialization, in late phase development (from clinical PoC onwards), clinical trial management, post-approval studies, regulatory and manufacturing compliance
  • Experience leading teams in a complex, matrixed, global and multi-disciplinary organization with high accountability, minimal authority and multiple lines of reporting
  • Experience working with regulators and with regulatory requirements including legal and government frameworks within and across global geographies
  • Experience creating the strategy for pre- and post-marketing studies and driving the lifecycle process
  • Experience building budgets and leading the strategic and budget planning process
  • Experience the healthcare environment, and access in all major markets

Nice to have:

  • Highly developed ethics and integrity, with demonstrated ethical medical decision-making skills
  • Strong matrix leadership and motivational skills
  • Ability to work collaboratively and successfully across functions – Research, Commercial, Regulatory, Global Medicine Supply, Legal, regions etc.
What we offer:
  • Annual bonus
  • Eligibility to participate in our share based long term incentive program
  • Health care and other insurance benefits (for employee and family)
  • Retirement benefits
  • Paid holidays
  • Vacation
  • Paid caregiver/parental and medical leave

Additional Information:

Job Posted:
January 07, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Icon
GSK - All Job Offers
Job Link Share:
Copy Link Icon
Facebook Icon Twitter Icon LinkedIn Icon

Looking for more opportunities? Search for other job offers that match your skills and interests.

Briefcase Icon

Similar Jobs for Executive Director, Medicine Development Leader

New

Director, Oncology Clinical Biomarkers

In this role, you will be responsible for the development and effective implemen...
Location
Location
United States; United Kingdom , Collegeville; London; Stevenage; Waltham
Salary
Salary:
189750.00 - 316250.00 USD / Year
us.gsk.com Logo
GSK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD in Life Sciences or Medical degree
  • Minimum of 5 years of experience in the pharmaceutical industry, with a solid background in oncology clinical biomarkers -expertise in late-phase oncology studies- and translational research within clinical development
  • Experience in leading cross-functional teams and executing strategic biomarker plans
  • Experience in conducting clinical trials and working as part of clinical study teams
  • Expertise in interpreting clinical biomarker data and evaluating innovative biomarker technologies for clinical trial applications
  • Experience in influencing teams and key leaders
Job Responsibility
Job Responsibility
  • Collaborating closely with the Clinical Biomarker Executive Director to drive the design, alignment, and execution of clinical biomarker and translational medicine strategies focused on identifying predictive biomarkers that enable clinical success
  • Validating and implementing biomarker strategies, including target engagement, pharmacodynamic, and proof-of-mechanism biomarkers, for clinical-phase programs to support patient stratification, dose selection, and enable clinical go/no-go decisions
  • Participating in tumor-specific Biomarker Matrix teams, with responsibility for executing clinical biomarker strategies for late-stage oncology programs, while working closely with internal and external stakeholders, as well as disease area strategy teams
  • Representing Translational Medicine at Clinical Development Matrix Teams (CMT) to establish biomarker-driven decision-making criteria and their seamless integration into clinical study designs, aligning with clinical study objectives
  • Identifying cutting-edge science and technological advances to incorporate into biomarker strategies for guiding indication selection, patient enrichment, and combination strategies
  • Overseeing and/or developing sample testing plans and delivering high-quality biomarker data packages to inform clinical development and regulatory strategies
  • Managing effective relationships with clinical and scientific operations, diagnostics, medical science, medical affairs, regulatory, portfolio management, and commercial functions
  • Supporting the expansion of mechanism and disease understanding to generate insights for indication expansion and scientific exchange as needed
  • Contributing to the company’s scientific credibility through publications and presentations
What we offer
What we offer
  • Competitive base salary
  • Annual bonus based on company performance
  • Flexible working options available for most roles
  • Learning and career development
  • Access to healthcare & wellbeing programmes
  • Employee recognition programmes
  • Health care and other insurance benefits (for employee and family)
  • Retirement benefits
  • Paid holidays
  • Vacation
  • Fulltime
Read More
Arrow Right

Associate Director, Medical Affairs (Scientific Communications/Publications)

We are seeking a detail-oriented and proactive Associate Director, Medical Affai...
Location
Location
United States , Philadelphia
Salary
Salary:
Not provided
cabalettabio.com Logo
Cabaletta Bio Inc
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Master’s degree in Health Care, Life Sciences, Biomedical Sciences, or a related field
  • >3 years of experience in medical affairs, scientific communications, or publication planning within the biotechnology or pharmaceutical industry
  • Therapy area experience in rheumatology, neurology, immunology, and/or cell therapy
  • Experience working with publications management software/vendors (such as iEnvision, PubStrat, PubPro)
  • Experience managing a publications or asset/project budget including overseeing external vendors
  • Strong scientific writing skills with the ability to translate complex scientific data into clear and concise publications, including ability to analyze and interpret clinical trial data
  • Knowledge of publication guidelines (e.g., ICMJE, GPP2022) and industry best practices
  • Excellent organizational skills with the ability to manage multiple projects simultaneously and meet deadlines
  • Proficiency in Microsoft 365 (Word, Excel, PowerPoint, OneNote)
  • Ability to travel up to 25% to attend conferences and meetings
Job Responsibility
Job Responsibility
  • Manage the end-to-end process of publication planning, ensuring adherence to timelines and compliance with industry standards
  • Collaborate with cross-functional teams, including Clinical Development, Translational Medicine, Computational Biology, Regulatory Affairs, and external authors/key opinion leaders, and vendors, to facilitate the development of manuscripts, abstracts, posters, and presentations
  • Manage the operational execution and day-to-day budget for external medical writing and communications agencies that support content and publication deliverables
  • Lead the preparation of journal manuscripts and abstracts and presentations for medical conferences, ensuring compliance with conference guidelines and requirements
  • Advise teams regarding compliance with medical publications as defined in journal and congress guidelines
  • Coordinate internal review processes and facilitate approval workflows for publications in collaboration with Legal, Compliance, and Medical teams
  • Train internal teams on publications software and workflows
  • Assist in the preparation of scientific content for medical conferences and other scientific forums
  • Maintain awareness of industry trends and regulatory guidelines related to publication practices in the biopharmaceutical industry
  • Develop and execute comprehensive scientific engagement strategies and congress plans (i.e. manage relationships with conference organizers, lead internal pre/post congress meetings, organize onsite HCP meetings, etc.)
What we offer
What we offer
  • health and retirement
  • PTO
  • stock option plans
Read More
Arrow Right

Translational Medicine Sr. Director

Join Enveda as a Translational Medicine Sr. Director, ENV-308 in a remote capaci...
Location
Location
United States
Salary
Salary:
300000.00 - 325000.00 USD / Year
enveda.com Logo
Enveda
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Ph.D., M.D., or equivalent advanced degree in pharmacology, biomedical sciences, or a related field
  • Minimum of 10 years of experience in translational medicine and / or biomarker strategy within the biotechnology or pharmaceutical industry
  • Minimum of 5 years focused on metabolism / metabolic disease programs with at least some experience in Obesity and Diabetes with a strong scientific grounding in energy balance, appetite regulation, and metabolic adaptation
  • Proven track record of successfully leading translational programs from discovery through clinical development
  • Deep understanding of PK/PD principles, biomarker development, and their application in drug development
  • Strong leadership skills with the ability to influence cross-functional teams and drive strategic initiatives
  • Excellent communication and interpersonal skills, with a demonstrated ability to present complex scientific concepts to diverse audiences
  • Experience with regulatory interactions and knowledge of the regulatory requirements for biomarkers and translational endpoints
Job Responsibility
Job Responsibility
  • Own End-to-End Translational Scope for ENV-308: Lead the translational strategy across preclinical and clinical development, with clear ownership for how human biology informs program direction, risk, and value
  • Define Biomarker & MOA Strategy: In collaboration with our MOA and pre-clinical teams, develop and prioritize biomarker and MOA hypotheses, including trial, experiment and assay design to support development decisions and differentiate ENV-308
  • Execute Translational Analyses: Take a hands-on role in analyzing and interpreting clinical, biomarker, and translational data in real time to guide active program decisions
  • Make High-Impact Scientific Judgments: Apply independent scientific judgment to translational decisions that shape the development path and differentiation strategy
  • Lead External Vendor Scientific Oversight: Evaluate, select, and scientifically guide translational and biomarker vendors from feasibility through data delivery
  • Create Decision-Enabling Readouts: Ensure biomarker and translational outputs are high-quality, interpretable, and designed to support clear program decisions
  • Integrate Data into Program and Regulatory Decisions: Synthesize translational and clinical evidence into go/no-go recommendations and contribute translational input to INDs, protocols, and internal reviews
  • Operate as an Asset-Embedded Program Leader: Work as a peer within the program leadership team, embedding translational thinking into clinical design, development sequencing, and portfolio trade-offs
What we offer
What we offer
  • 90% Medical, Dental, Vision
  • 401k Match
  • Flexible PTO
  • Adoption Assistance
  • Fulltime
Read More
Arrow Right
New

Head of Clinical Practice – Forensic Healthcare, Primary Care and Community Services

The Head of Clinical Practice provides senior, strategic clinical leadership acr...
Location
Location
United Kingdom
Salary
Salary:
70000.00 GBP / Year
phlgroup.co.uk Logo
Partnering Health
Expiration Date
May 15, 2026
Flip Icon
Requirements
Requirements
  • Registered healthcare professional (NMC, HCPC or GMC)
  • Significant senior clinical leadership experience in forensic healthcare, custody medicine or similarly high-risk environments
  • Strong working knowledge of FFLM guidance and custody healthcare systems
  • Experience of clinical governance, risk management and patient safety
  • Experience leading multidisciplinary clinical teams including FMEs, HCPs and doctors
  • Experience of workforce stabilisation or service improvement in complex environments
Job Responsibility
Job Responsibility
  • Set the clinical vision and standards for forensic healthcare services
  • Provide clinical assurance that care in custodial environments is safe, lawful and aligned to equivalence principles
  • Define and maintain organisation-wide forensic clinical practice standards
  • Lead clinical preparedness for external scrutiny
  • Champion high-quality clinical decision-making and professional standards in custody settings
  • Direct the clinical risk agenda for forensic services
  • Embed trauma-informed and compassionate approaches across forensic pathways
  • Set the clinical direction and standards for Primary Care services
  • Develop clinical leadership capacity within Primary Care and ADHD directorates
  • Assure safe clinical systems across Primary Care
What we offer
What we offer
  • Bike2Work Scheme
  • DSE Eye Tests and Spectacles
  • Employee Assistance Program – 24 hour helpline
  • Employee Recognition
  • Family Friendly Policy
  • Long Service Award
  • Menopause Support
  • NHS Discount – Blue Light Card
  • Paid Sick Pay
  • Professional Development
  • Fulltime
Read More
Arrow Right

Director, Global Content Design and Delivery, Oncology

The Director, Global Content Design and Delivery, Oncology in the Global Scienti...
Location
Location
United States; Switzerland; United Kingdom , Collegeville; Baar; Durham; London; Philadelphia; Upper Providence
Salary
Salary:
Not provided
us.gsk.com Logo
GSK
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Advanced degree in science, medicine, pharmacy, communications or a related field
  • 7+ years of related experience in scientific communications, medical content design and delivery, or a related field within the pharmaceutical or healthcare industry
  • Experience in leading cross-functional teams and driving strategic communication plans
  • Mastery developing and executing innovative communication tools, including digital and social media strategies
  • Project management expertise with multiple projects simultaneously, meeting deadlines
  • Experience in developing and delivering medical training materials
  • Proficiency in digital content creation and management tools with solid technical capabilities in Excel, PowerPoint, and Team sites
  • Interpreting, analyzing, organizing, and presenting complex data to a broad range of audiences required
Job Responsibility
Job Responsibility
  • Chair the Global Integrated Medical Communication Teams (GIMCT) for assigned assets/therapeutic areas to drive the development of Integrated Medical Communication Plans (IMCP), inclusive of content, channel, and congress plans/tactics
  • Drive key asset deliverables including the Scientific Communication Platform (SCP), Scientific Narratives, Content and Channel plans, Congress Plans and all associated tactics
  • Serve as a key partner to therapeutic area medical leaders, global publications, R&D, Global Medical Team (GMT), and priority markets and regions
  • Collaborate with internal stakeholders on the development and execution of innovative tools for internal and external communication, including digital/social medical delivery
  • Drive timely execution of all deliverables within the IMCPs for assigned assets, ensuring they are scientifically accurate, evidence-based, and comply with relevant regulations, industry guidelines, and ethical standards
  • Accountable for aligning with key stakeholders and for the input of the IMCP framework and related engagement planning elements within the asset annual business planning process
  • Lead annual scope of work development with procurement for IMCP deliverables with agencies of record, and provide continuous oversight and feedback to drive effective collaboration and partnership
  • Ensure content development follows all relevant codes and system requirements (e.g. ABPI code of practice, GSK Code, and use of Content Lab), particularly with respect to the delivery of promotional versus non-promotional information
  • Participate in initiatives on Gen AI platforms being leveraged for content creation and personalization/adaptation to ensure broader scalability and use
  • Gather and share best practices across Global to ensure consistency, high standards, and excellence are maintained across the organization
What we offer
What we offer
  • Competitive base salary
  • Annual bonus based on company performance
  • Flexible working options available for most roles
  • Learning and career development
  • Access to healthcare & wellbeing programmes
  • Employee recognition programmes
  • Fulltime
Read More
Arrow Right

Medical Director-Health Care Delivery, Clinical Perf-At Home

At CVS Health, we’re building a world of health around every consumer and surrou...
Location
Location
United States , Illinois
Salary
Salary:
174070.00 - 374920.00 USD / Year
https://www.cvshealth.com/ Logo
CVS Health
Expiration Date
July 01, 2026
Flip Icon
Requirements
Requirements
  • M.D. / D.O. in good standing with no restrictions required
  • Board certification in Internal Medicine or Family Medicine required for M.D. or D.O., Board certification in Family, Adult, or Gerontology for A.P.N.
  • Experience in clinical leadership roles, leading and coaching providers to be the best they can be for their patients and their colleagues
  • Experience using a metrics-driven approach to the provision of medical care and/or quality projects
  • 5+ years of experience in outpatient practice preferred
  • Providers who have been at OSH for a minimum of 1 year are welcome to apply
  • Fellowship training in Geriatrics and/or other professional degrees (e.g., M.B.A., J.D., M.P.H.) welcome but not required
  • Working knowledge of adult learning and prior experience of developing lectures and presentations for remote and in-person learners
  • Willingness to shadow and conduct patient visits, as needed, to test workflows and clinical skills in direct patient care settings
  • Minimum of 1 year in roles coaching providers and their teams to provide exemplary care
Job Responsibility
Job Responsibility
  • Onboarding
  • Content Development
  • Clinical development
What we offer
What we offer
  • Mission-focused career impacting change and measurably improving health outcomes for Medicare patients
  • Paid vacation, sick time, and investment/retirement 401K match options
  • Health insurance, vision, and dental benefits
  • Opportunities for leadership development and continuing education stipends
  • New centers and flexible work environments
  • Opportunities for high levels of responsibility and rapid advancement
  • Fulltime
Read More
Arrow Right

Director, Payer Policy

The Director, Payer Policy is responsible for shaping, influencing, and executin...
Location
Location
United States
Salary
Salary:
164900.00 - 247000.00 USD / Year
neogenomics.com Logo
NeoGenomics Laboratories
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • Bachelor’s degree in Business, Health Policy, Science, or related field required
  • Advanced degree (MBA, MPH, MHA, MS, PharmD, PhD) preferred
  • 10 years’ experience required in of payer relations, market access, reimbursement, or managed care leadership, preferably within diagnostics, laboratory services, or biotech
  • Deep expertise in payer policy, coding, coverage frameworks, and reimbursement economics
  • Demonstrated experience influencing coverage decisions and navigating LBM organizations
  • Strong understanding of oncology testing, precision medicine, and relevant regulatory pathways
  • Proven track record of leading cross-functional teams in complex, matrixed environments
  • Experience shaping evidence strategy and collaborating with Medical Affairs/HEOR teams preferred
  • Experience in laboratory or diagnostic reimbursement environments preferred
Job Responsibility
Job Responsibility
  • Develop and execute a multi-year payer strategy to secure broad, durable coverage for NeoGenomics’ oncology diagnostic portfolio
  • Lead payer policy engagement, including proactive outreach, policy reviews, coverage advocacy, and targeted education on new and emerging technologies
  • Define and communicate NeoGenomics’ payer value proposition, leveraging clinical evidence, HEOR, real-world data, and patient outcomes
  • Partner with Medical Affairs, Clinical, and R&D to influence evidence plans needed to support positive coverage decisions
  • Oversee payer policy monitoring and regulatory surveillance
  • communicate changes and recommended actions to internal stakeholders
  • Ensure payer contracts, policies, and billing operations are fully aligned to maximize reimbursement yield and reduce leakage
  • Advocate directly with payer Medical Directors, policy teams, and LBMs to support positive coverage and overturn restrictive decisions
  • Develop and present scientifically grounded, evidence-based dossiers and materials tailored to payer needs
  • Support preparation of clinical, economic, and outcomes evidence that strengthens the payer value story
What we offer
What we offer
  • Career coaches
  • Many training opportunities
  • Highly competitive benefits with a variety of HMO and PPO options
  • Company 401k match
  • Employee Stock Purchase Program
  • Tuition reimbursement
  • Leadership development
  • 16 days of paid time off plus holidays
  • Wellness courses
  • Highly engaged employee resource groups
  • Fulltime
Read More
Arrow Right

Senior Director, Molecular Pathology and Cell Biology

Moderna is seeking a strategic and scientifically rigorous leader to serve as Sr...
Location
Location
United States , Cambridge
Salary
Salary:
196700.00 - 353400.00 USD / Year
modernatx.com Logo
Moderna
Expiration Date
Until further notice
Flip Icon
Requirements
Requirements
  • PhD, MD, or equivalent in Pathology, Cell Biology, Immunology, Cancer Biology, or related discipline
  • 12+ years of experience in translational research, molecular pathology, or functional cell biology within biotech, pharma, or academia
  • Strong understanding of advanced tissue-based assay strategies, including highly multiplexed spatial profiling approaches and AI-powered image analysis
  • Significant experience in cell-based functional assays, including cytotoxicity and immune effector assays
  • Experience building and deploying advanced experimental model systems (3D cultures, explants, co-culture platforms)
  • Demonstrated experience supporting translational research programs and contributing to development-stage decision-making
  • Proven leadership of multidisciplinary scientific teams within a matrixed organization
  • Strong communication skills and ability to influence across Research and Development functions
Job Responsibility
Job Responsibility
  • Lead and integrate high-performing Molecular Pathology and Cell Biology teams while defining and executing a forward-looking translational strategy aligned with therapeutic area priorities and portfolio needs
  • Serve as a scientific thought partner to Research, Translational Medicine, and Clinical Biomarker leaders, shaping priorities and enabling effective cross-functional collaboration
  • Set the strategic direction for Molecular Pathology support of target and tissue expression profiling across normal and disease tissues to inform target selection, program prioritization, and translational hypothesis development
  • Guide the deployment of routine and advanced tissue-based assays, novel spatial profiling approaches, and the continued evolution of the digital pathology infrastructure to ensure fit-for-purpose application across programs
  • Oversee development and execution of cell-based functional assays including cytotoxicity, cell-killing, ADCC, and pathway interrogation assays
  • Drive innovation in advanced experimental model systems including organoids, patient-derived explants, and co-culture systems
  • Establish quality standards, reproducible workflows, and scalable infrastructure to deliver high-quality data supporting Therapeutics Research, Translational Medicine, and, when appropriate, IND-enabling efforts
What we offer
What we offer
  • Best-in-class healthcare coverage, plus voluntary benefit programs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Family planning benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investment opportunities to help you plan for the future
  • Location-specific perks and extras
  • Eligible for an annual discretionary bonus, other incentive compensation, or equity award
  • Fulltime
Read More
Arrow Right