HEOR Operational Study Manager (3 roles) jobs

Showing 25+ verified jobs

Browse locationsLocations Create alert

query:HEOR Operational Study Manager (3 roles)

Arine

HEOR Researcher

RemoteRemoteMid Level$130K–150K

posted last month

Komodo Health

Principal, Product Strategy (RWE/HEOR)

United States$245K–288K

posted 17 days ago

Beacon Biosignals

Clinical Study Operations Manager

Boston, United StatesRemote$90K–110K

posted 4 days ago

careers heart

Operations Manager, Clinical Studies

Dallas, United Statesfull timeMid Level

posted 2 months ago

EVERSANA

Manager, HEOR

Toronto, CanadaRemotefull timeDirector

posted 2 months ago

Motive

Role Readiness Operations Manager

Remote, United StatesRemote

posted 15 days ago

Lifelancer | Career Page

Local Study Operations Manager TA Head

Job Openings Local Study Operations Manager TA Head About the job Local Study Operations Manager TA Head Job Title: Local Study Operations Manager TA Head Job Location: Washington D.C., District of Columbia, United States Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.Local Study Operations Manager TA HeadWhat you will doLet’s do this. Let’s change the world. In this role, you will lead and develop Local Study Operations Senior Managers, strengthening their leadership capabilities, functional expertise, and overall performance to ensure alignment with both global and country-level objectives. You will oversee the successful delivery of the country’s study portfolio—managing scope, timelines, and budgets—through effective guidance and support of the LSOM Senior Manager team. Working closely with the Country GSSO Head, you will help cultivate a strong clinical research environment that supports global R&D priorities. Additionally, you will drive strategic alignment and continuous improvement by standardizing processes across LSOM Senior Managers, promoting best practices, encouraging digital innovation, and facilitating the systematic sharing of knowledge and lessons learned across teams.Ensure the accountable delivery of the study portfolio assigned to LSOM Senior Managers.Oversee and guide the country study portfolio through effective leadership of LSOM Senior Managers, aligning execution with global strategies and local priorities.Provide strategic direction and support to LSOM Senior Managers in portfolio monitoring, driving local action plans, and resolving issues.Serve as the primary escalation point for complex or systemic local study challenges, facilitating resolution and ensuring portfolio targets are met with quality and efficiency.Lead the development and mentorship of LSOM Senior Managers to equip them for effective team leadership and operational excellence.Build and maintain a high-performing leadership team that promotes accountability, collaboration, and resilience across the LSOM organization.Facilitate close collaboration between global study strategy teams and local study teams to effectively manage the assigned portfolio.Oversee coordination among country functional teams to ensure successful delivery of the country portfolio.Support discussions on country study placements, considering country strengths and growth potential.Act as a key advisor for site selection, identifying priority sites and allocating resources accordingly.Support country-level risk assessments by proactively identifying and managing risks to delivery.Ensure inspection readiness and provide hands-on support during inspections, including responsibility for storyboards.Promote continuous operational improvements and encourage sharing of best practices.Manage resource allocation and workload distribution among LSOM Senior Managers and the broader LSOM team, including both FSP and FTE, to optimize trial execution and align with global priorities.Ensure compliance with relevant regulatory and quality standards.Collaborate with the country head to engage cross-functional stakeholders, align on trial deliverables, and manage escalations as needed.What we expect of youWe are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an individual with the following qualifications.Basic Qualifications:Doctorate degree and 3 years of clinical execution experience ORMaster’s degree and 7 years of clinical execution experience ORBachelor’s degree and 9 years of clinical execution experience ORAssociate’s degree and 12 years of clinical execution experience ORHigh school diploma / GED and 14 years of clinical execution experienceIn addition to meeting at least one of the above requirements, you must have a minimum of 3 years of experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Your managerial experience may run concurrently with the required technical experience referenced abovePreferred Qualifications:+8 years work experience in life sciences or medically related field, including 6 years of biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company)Experience managing multiple teams / direct reportsExperience at or oversight of outside clinical research vendors (CRO’s, central labs, imaging vendors, etc.)Experience working on global clinical trials, with highly effective communications skills and track record for improving site engagement, improving relationships with investigators, and operational efficiencyWhat you can expect of usAs we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.The annual base salary range for this opportunity in the U.S. is $167,187-$226,194.In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.A discretionary annual bonus program, or for field sales representatives, a sales-based incentive planStock-based long-term incentivesAward-winning time-off plans and bi-annual company-wide shutdownsFlexible work models, including remote work arrangements, where possibleApply nowfor a career that defies imaginationObjects in your future are closer than they appear. Join us.careers.amgen.comAs an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Apply for Position Or refer someone Share Facebook Line LinkedIn X (Formerly Twitter) Whatsapp EmailRemote$167.2K–226.2K

posted 19 hours ago

Apple

Clinical Study Operations Engineering Program Manager - Health

Sunnyvale, United StatesSenior

posted 2 months ago

Medtronic

HEOR Specialist

Warsaw, Polandfull timeMid Level

posted 2 months ago

Beacon Biosignals

Clinical Study Operations Associate

RemoteRemote$65K–85K

posted 3 days ago

EVERSANA

Associate Director, HEOR

Burlington, ON, CanadaRemotefull timeDirector

verified Jun 11, 2026posted 3 months ago

WNS Global Services

Healthcare Support Roles - Operations Supervisor / Manager (PHRN / USRN)

Quezon City, NCR, Philippinesfull timeMid Level

posted 3 months ago

Lifelancer | Career Page

Local Study Operations Line Sr. Manager

Job Openings Local Study Operations Line Sr. Manager About the job Local Study Operations Line Sr. Manager Job Title: Local Study Operations Line Sr. Manager Job Location: Washington D.C., District of Columbia, United States Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Join Amgen’s Mission of Serving PatientsAt Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.Local Study Operations Line Sr. Manager What you will doLet’s do this. Let’s change the world. . Let’s change the world. In this role, you will lead the skill development of Local Study Operations Managers, ensuring effective trial implementation within the country and strong alignment with global strategies. You will oversee the delivery of the country’s study portfolio—managing scope, timelines, and budgets—through the leadership of LSOM. Working in close partnership with the Country GSSO Head, you will help foster, enhance, and sustain an optimal clinical research environment that supports global R&D objectives. Additionally, you will drive alignment and continuous improvement in LSOM execution by integrating best practices, promoting digital innovation, and facilitating robust knowledge sharing across the team.Ensure the successful delivery of the study portfolio assigned to LSOMs.Oversee LSOMs’ fulfillment of responsibilities throughout the assigned country portfolio, from feasibility through to study close-out.Monitor portfolio progress, provide risk and quality oversight, and support issue escalation and resolution for LSOMs.Manage LSOM and LSOM vendor performance to guarantee high-quality study execution, serving as the primary escalation point for local study challenges, driving solutions, and ensuring portfolio targets are met within the country.Mentor, train, and support the professional development of LSOMs to prepare them for managing complex trials.Build and maintain a high-performing team.Facilitate close collaboration between the study strategy team and local study teams to effectively manage the assigned portfolio.Promote cross-functional collaboration among country teams to ensure successful delivery of the country portfolio.Support discussions regarding study placement decisions based on country capabilities and growth potential.Proactively evaluate risks, quality trends, and resource requirements; implement mitigation strategies and drive continuous improvement in country operations.Lead initiatives to enhance operational efficiency and encourage sharing of best practices.Manage resource allocation and workload distribution across LSOMs, including both FSP and FTE personnel, to optimize trial execution and align with global priorities.Ensure adherence to regulatory and quality standards where applicable.Collaborate with and support the country head in engaging cross-functional stakeholders, aligning on trial deliverables, and managing escalations.What we expect of youWe are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an individual with the following qualifications.Basic Qualifications:Doctorate degree & 2 years of clinical execution experience ORMaster’s degree & 6 years of clinical execution experience ORBachelor’s degree & 8 years of clinical execution experience ORAssociate’s degree & 10 years of clinical execution experience ORHigh school diploma / GED & 12 years of clinical execution experienceIn addition to meeting at least one of the above requirements, you must have a minimum of 2 years experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation of resources. Your managerial experience may run concurrently with the required technical experience referenced abovePreferred Qualifications:7 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO companyExperience managing multiple teams / direct reports across multiple clinical functions / trialsExperience at, or oversight of, clinical research vendors (CRO’s, central labs, imaging vendors, etc.)Experience managing clinical operations across relevant geography / region, including strong understanding of local regulatory requirements around global clinical trialsWhat you can expect of usAs we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is $151,988 - $205,630. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accountsA discretionary annual bonus program, or for field sales representatives, a sales-based incentive planStock-based long-term incentivesAward-winning time-off plansFlexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.Apply now and make a lasting impact with the Amgen team.careers.amgen.comIn any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.Application deadlineAmgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.SponsorshipSponsorship for this role is not guaranteed.As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Apply for Position Or refer someone Share Facebook Line LinkedIn X (Formerly Twitter) Whatsapp EmailRemote$152K–205.6K

posted 19 hours ago

AbbVie

Director, HEOR Strategy, Migraine

Mettawa, IL, United Statesfull timeDirector

posted 23 days ago

Novartis

BSI HEAD HEOR

Hyderabad, Indiafull timeExecutive

posted 29 days ago

Lifelancer | Career Page

Project Manager, Market Access & HEOR - Syneos Health Careers

Job Openings Project Manager, Market Access & HEOR - Syneos Health Careers About the job Project Manager, Market Access & HEOR - Syneos Health Careers Job Title: Project Manager, Market Access & HEOR - Syneos Health Careers Job Location: Remote - Canada Job Location Type: Remote Job Contract Type: Full-time Job Seniority Level: Description We are looking for a seasoned market access and HEOR project manager with solid experience of Canadian and North American pharmaceutical markets, payer environments, and consulting dynamics.Areas of responsibility will include managing client projects end-to-end, ensuring milestones are met on time, and advising clients on complex market access needs-such as commercialization, entity establishment, pricing (PMPRB and pCPA), HTA submissions (CDA and INESSS), provincial and private drug plans, health systems, and patient support programs (PSPs). The project manager will lead client projects, direct project teams, support clients with strategic advisory with minimal to no supervision.In addition to having a solid experience in market access and project management, the right individual will also bring HEOR experience, such as overseeing evidence synthesis, reviewing submission dossiers, AMCP dossiers, developing patient journey assessment, conducting primary market research (PMR), reviewing and developing economic models (such as budget impact and cost-effectiveness models), writing and editing reports and presenting findings to various reimbursement agencies and clients. Knowledge of the US healthcare setting is very important.Here is what you will need to be successful:Education and ExperienceMaster’s degree in a quantitative discipline (such as Health Economics, Pharmacoeconomics, or Biostatistics) is required5-7 years of relevant professional experience, or combination of experience and a higher degree in a related fieldExperience managing Canadian and US payer evidence and access projects are requiredDirect experience in the preparation of submission dossiers for private and public reimbursement submissions is requiredKnowledge and SkillsDeep knowledge of the Canadian and US health care systems, including public/private payer pathways, PMPRB regulations, the pCPA negotiation process, and PSP setups in CanadaStrong consulting background with the ability to act as a primary strategic advisor to clients on commercialization, launch readiness, and legal entity establishmentAbility to manage client work independently and conduct critical appraisal and quality assurance on client-facing and payer-related market access and HEOR materialsAbility to work independently as well as in a team environmentProven project management and team leadership skills Excellent verbal and written communication skills; excellent presentation skillsLocation: Anywhere in Canada (currently remote/home-based; subject to change). Candidates must be legally authorized to work in Canada.At Syneos Health, we are dedicated to building a diverse, inclusive and authentic workplace. If your past experience doesn’t align perfectly, we encourage you to apply anyway. At times, we will consider transferable skills from previous roles. We also encourage you to join our Talent Network to stay connected to additional career opportunities.Why Syneos Health? Here, you’re a part of the big picture. You will collaborate with colleagues across clinical and commercial disciplines to guide premarket development through post-market commercial strategy. Every project is a chance to solve a new challenge, learn from your colleagues, and advance your career. The diversification and breadth of our new and existing partnerships create a multitude of career paths and employment opportunities. Join our game-changing, global company dedicated to creating better, smarter, faster ways to get biopharmaceutical therapies to patients. Experience the thrill of knowing that your everyday efforts are contributing to improving patients’ lives around the world. Work Here Matters Everywhere | How are you inspired to change lives?Syneos Health companies are affirmative action/equal opportunity employers (Minorities/Females/Veterans/Disabled) This job is curated by Lifelancer. Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains. Please apply via Lifelancer platform to get connected to the application page and to find similar roles. Apply for Position Or refer someone Share Facebook Line LinkedIn X (Formerly Twitter) Whatsapp EmailRemote

posted 9 days ago

Novartis