50 Biopharmaceutical Leadership jobs in Remote - United States.

Hiring now: Associate Dir Regulatory @ Orca Bio, Sr Medical Science Liaiso @ Biogen, Proposal And Contract Mgr @ Parexel, Staff Medical Science Lia @ Guardanthe, Dir Statistical Programmi @ Arcus Bios, Clinical Spec @ Symmetrio, Medical Monitor @ Psi, Sr Oncology Medical Scien @ Kyowa Kiri, Global Pharmacovigilance @ Amgen, Clinical Trials Asst Cta @ Iqvia.Explore more at jobswithgpt.com.

🔥 Skills

clinical trials (9) clinical research (6) compliance (6) Medical Science Liaison (5) oncology (5) clinical studies (5) project management (5) regulatory strategies (4) Research (4) Drug Development (4)

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United States (50)
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Orca Bio

Associate Director, Regulatory Affairs United States
Skills & Focus: biotechnology, regulatory affairs, promotional materials, cell therapies, cross-functional, regulatory strategies, submissions, graft vs. host disease, matrixed environment, commercial planning
About the Company: Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing signif…
Type: Full-time
Associate Director, Regulatory Affairs United States
Skills & Focus: biotechnology, regulatory affairs, promotional materials, cell therapies, cross-functional, regulatory strategies, submissions, graft vs. host disease, matrixed environment, commercial planning
About the Company: Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing signif…
Type: Full-time

Biogen

(Sr) Medical Science Liaison United States
Skills & Focus: Medical Science Liaison, clinical decisions, Key Medical Experts, healthcare professionals, stakeholder engagement, strategic relationships, medical community, medical excellence, KME engagement plans, medical insights
About the Company: Biogen is a global biotechnology company specializing in discovering, developing, and delivering innovative therapies for neurological and neurodegenerative di…
Type: Full-time

Parexel

Proposal and Contract Manager United States
Skills & Focus: Proposal, Contract, Manager, Remote, Clinical, Research, Biopharmaceutical, Consulting, Regulatory, Drug Development
About the Company: Parexel is a global biopharmaceutical services organization that provides a comprehensive range of drug development and regulatory consulting services.
Type: Full-time
Various Regulatory Affairs and Consulting Roles United States
Skills & Focus: Regulatory Affairs, Biologics, Clinical Research, Project Management, Consulting, Technical, Medical Device, Strategy, Drug Development, Clinical Trials
About the Company: Parexel is a global biopharmaceutical services organization that provides services to the pharmaceutical, biotechnology, and medical device industries.
Type: Full-time
Solution Consultant Associate Director/Director/Senior Director United States
Skills & Focus: Sales, Clinical Research, Consulting, Project Management, Biostatistics, Statistical Programming, Medical Writing, Safety Solutions, Account Management, Enterprise Sales
About the Company: Parexel is dedicated to advancing science by keeping the patients in mind, working towards building deeper connections with patients, and has a global approach…
Type: Remote

Guardanthealth

Staff Medical Science Liaison United States
Skills & Focus: Key Opinion Leaders, clinical expertise, educational materials, scientific events, sales teams, research collaborations, outreach campaigns, product adoption, Clinical Advisory Board, Guardant datasets

Parexel

Biomarker Sample Operations Associate United States
Skills & Focus: Biomarker, Sample, Operations, Associate, Clinical, Research, Medical, Data Management, Global, Health

Arcus Biosciences

Director, Statistical Programming United States
Skills & Focus: Statistical Programming, CDISC standards, FDA guidance, biostatistics, clinical trials, data management, analysis standards, programming standards, SAS, oncology
Experience: Minimum 12+ years of biotechnology or pharmaceutical experience
Salary: $225,000 - $250,000 USD annually
Benefits: opportunity to participate in stock programs, performance-based bonus, comprehensive benefits package

Symmetrio

Clinical Specialist United States
Skills & Focus: liver tumor ablation, clinical education, case support, training, interventional oncology, product adoption, clinical research, ablation technologies, communication, travel
About the Company: a medical device and software manufacturer
Experience: 3+ years of experience in interventional radiology, oncology, or liver tumor ablation
Salary: $120,000 to $150,000
Benefits: Health Care Plan (Medical, Dental & Vision), Retirement Plan (401k, IRA), Paid Time Off (Vacation, Sick & Public Holida…

Psi

Medical Monitor United States
Skills & Focus: Medical input, clinical studies, patient safety, regulatory agencies, clinical development plans, data safety monitoring, Pharmacovigilance, GCP guidelines, risk mitigation, clinical documents
About the Company: PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and…

Kyowa Kirin North America

Senior Oncology Medical Science Liaison- Great Lakes United States
Skills & Focus: Medical Science Liaison, pharmaceutical, oncology, stakeholder relationships, clinical research, educational resources, compliance, key opinion leaders, territory management, scientific communication
About the Company: Kyowa Kirin is a fast-growing global specialty pharmaceutical company that applies state-of-the-art biotechnologies to discover and deliver novel medicines in …
Experience: Minimum three (3) years MSL experience in pharmaceutical environment, preferably with an oncology therapeutic focus.
Salary: $165,000 – $180,000
Type: Full-time
Benefits: Medical, Dental & Vision Insurance, Life Insurance, Short- and Long-Term Disability Insurance, Flexible Spending Accoun…

Amgen

Global Pharmacovigilance (PV) Scientist United States
Skills & Focus: pharmacovigilance, safety assessment, signal detection, data analysis, regulatory inquiries, risk management, clinical trials, adverse event data, aggregate reports, medical research
About the Company: 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…
Experience: Minimum 3 years direct experience in pharmacovigilance.
Salary: 122,105.00 USD - 145,799.00 USD
Type: Full time
Benefits: From our commitment to professional and personal growth and well-being.

Iqvia

Clinical Trials Assistant (CTA) United States
Skills & Focus: Clinical Research, Trial Master File, administrative activities, regulatory compliance, clinical documents, clinical data, Microsoft Office, Good Clinical Practice, time management, communication
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: 3 years administrative support experience
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs.
Medical Writer (Consultant for HTA) United States
Skills & Focus: Medical Writing, HEOR, HTA, Clinical Assessment, Dossiers, Research, Analytics, Value Communications, Economics, Healthcare
About the Company: IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates int…
Experience: Significant experience in medical writing
Type: Full-time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Syneos Health

Mgr, Regulatory Consulting United States
Skills & Focus: regulatory submissions, project management, compliance, clinical reports, budgeting, staff management, pharmaceutical, medical writing, IND, PMA
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
Experience: Moderate experience in regulatory with demonstrated experience in contributing to the preparation of regulatory submissions.
Salary: $79,800-139,600 USD
Type: Full-time
Benefits: Health benefits to include Medical, Dental, and Vision, Company match 401k, eligibility to participate in Employee Stoc…
Regulatory Project Manager United States
Skills & Focus: regulatory submissions, project management, project teams, business development, budgets, clients, regulatory research, IND, pharmaceutical development, clinical reports
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Experience: Minimum of 8 years of experience in regulatory affairs or project management within the pharmaceutical/biotechnology industry.
Salary: $79,800 - $139,600
Benefits: Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock…

Novartis

Associate Clinical Research Medical Director - Immunology United States
Skills & Focus: clinical trials, clinical development, medical leadership, safety standards, clinical data quality, clinical trial operations, recruitment potential, insights, Informed Consent Forms, collaboration
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people's lives so that patients, healthcare profess…

Johnson & Johnson

Sr. Manager Clinical Marketing - Shockwave United States
Skills & Focus: clinical marketing, product management, cardiovascular medtech, Intravascular Lithotripsy, market adoption, competitive differentiation, sales force engagement, global marketing programs, clinical research, key opinion leaders
About the Company: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented,…
Experience: Minimum 10 years of professional product management or equivalent experience
Salary: 114,000.00 - 229,000.00 USD Annual
Type: Full-time
Benefits: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal …

Novartis

Senior Molecular Imaging Expert (Senior Principal Scientist) United States
Skills & Focus: Molecular Imaging, Clinical Trials, PET/SPECT, Biomarkers, Drug Development, Oncology, Efficacy, Safety, Translational Imaging, Clinical Imaging
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Experience: 5+ years of experience in PET/SPECT Imaging in academia or industry
Type: Full-time
Clinical Development Medical Director (CDMD) United States
Skills & Focus: clinical leadership, program management, data review, regulatory documents, trial data, safety reporting, clinical development plan, medical monitor, external partnerships, disease standards
About the Company: Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare profess…
Type: Full-time

Eikon Therapeutics

Senior Clinical Research Associate United States
Skills & Focus: clinical trials, monitoring, Good Clinical Practice, site management, Oncology, protocols, data integrity, inspection readiness, relationship management, Clinical Trial Management System
About the Company: Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biolog…
Experience: Typically requires a minimum of 8+ years of experience with a Bachelor's Degree, or 6+ years of experience with a Master's degree.
Salary: $130,000 to $142,500
Type: Full-time
Benefits: 401k plan with company matching, Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums cove…

Psi

Medical Monitor United States
Skills & Focus: clinical studies, medical matters, clinical development plans, safety monitoring, data safety monitoring boards, clinical data analysis, Pharmacovigilance, FDA compliance, ICH guidelines, GCP guidelines
About the Company: PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and…
Type: Full-time
Medical Monitor United States
Skills & Focus: clinical studies, medical matters, clinical development plans, safety monitoring, data safety monitoring boards, clinical data analysis, Pharmacovigilance, FDA compliance, ICH guidelines, GCP guidelines
About the Company: PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and…
Type: Full-time

Biomarin

Medical Director, Experimental Medicine United States
Skills & Focus: clinical development plans, phase 1 clinical trials, first-in-human, clinical research, IND filings, clinical trial protocols, biomarkers, medical monitor, cross-functional team, collaborative environment
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: 5+ years of hands-on experience in industry clinical trials
Salary: $220,000 to $330,000 per year
Type: Remote Only
Benefits: a discretionary bonus and/or long-term incentive units, full range of medical, financial, and/or other benefits

Guardanthealth

Staff Medical Science Liaison United States
Skills & Focus: Medical Science Liaison, Key Opinion Leaders, educational materials, scientific events, clinical expert, Advisory Board meetings, research collaborations, Guardant datasets, outreach campaigns, product adoption

Syneos Health

Principal Medical Writer- Regulatory United States
Skills & Focus: Medical Writing, Clinical Study Protocols, Data Presentation, Regulatory Standards, Team Collaboration, Clinical Reports, IND Submissions, NDA Submissions, Document Development, Interpersonal Skills
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…

Pfizer

Medical Lead, MD United States
Skills & Focus: Primary Care, Medical Lead, Medical Affairs, Promotional review, Patient needs, Cross-functional, Risk-management, Healthcare ecosystem, Telemedicine, Strategic thinking
Experience: 5+ years of relevant industry experience
Salary: $242,000 - $403,400
Type: Full time
Benefits: Comprehensive and generous benefits, participation in Pfizer’s Global Performance Plan, bonus target of 25.0% of base s…

Bridgebio Pharma

Director/Sr. Director, Regulatory Affairs - CMC United States
Skills & Focus: Regulatory Affairs, CMC, NDA, MAA, Documentation, Submissions, Compliance, Health Authority, Drug Development, Quality Control
About the Company: BridgeBio Pharma is a commercial stage biopharmaceutical company focused on addressing the large and growing unmet need in diseases caused by transthyretin, or…
Experience: Successful experience leading Regulatory CMC activities for multiple regulatory filings in pre-and post-approval settings, including experience filing an NDA/MAA for a new chemical entity.
Salary: $210,000 - $315,000 USD
Type: Full-time
Benefits: A robust and market-competitive compensation & benefits package including base pay, annual performance bonus, company e…

Amgen

Clinical Research Medical Director, Blinatumomab United States
Skills & Focus: clinical research, Blinatumomab, clinical expert, protocol development, safety and regulatory interactions, clinical trial data, publications, key opinion leaders, clinical input, Good Clinical Practices
About the Company: 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…
Experience: 2 years of clinical research experience and/or basic science research
Salary: 261,969.00 USD - 329,723.00 USD
Type: Full time
Benefits: Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, g…

Legend Biotech

Associate Director Medical Affairs Training United States
Skills & Focus: Medical Affairs, training, scientific initiatives, ciltacabtagene autoleucel, biopharmaceutical, collaboration, KOL engagement, congress preparation, knowledge assessment, project management
About the Company: Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inc…
Experience: 2+ years of experience in Medical Affairs or training within the biopharmaceutical industry preferred

Ascendis Pharma

Medical Science Liaison United States
Skills & Focus: Medical Science Liaison, Endocrinology, KOLs, clinical expertise, medical profession, scientific expertise, patient advocacy, clinical data presentations, investigator-initiated trials, CRM platform
About the Company: Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States that is using its TransCon…
Experience: Minimum 5+ years of pharmaceutical experience as a medical science liaison required
Benefits: 401(k) plan with company match, Medical, dental, and vision plans, Life and AD&D insurance, Short and long-term disabil…

Iqvia

Clinical Trial Educator – Cardiovascular United States
Skills & Focus: Clinical Trials, Patient Enrollment, In-Service Presentations, Referral Networks, Community Engagement, Interpersonal Skills, Customer Service, Data Abstraction, Travel, Healthcare
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industrie…
Experience: Clinical Research experience required
Salary: $74,900.00 - $124,800.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Precisionmedicinegroup

Regulatory and Start Up Specialist United States
Skills & Focus: clinical trial submission, regulatory, IRB, contract negotiation, site start-up, compliance, Clinical Trial Application Forms, Essential Document collection, budget negotiation, project plans

Amgen

Sr. Manager IVD Strategy & Operations - Precision Medicine Unit United States
Skills & Focus: IVD, strategy, operations, regulatory, cross-functional, coordination, training, performance tracking, collaboration, change management
About the Company: Amgen's shared mission is to serve patients living with serious illnesses, pioneering the world of biotech since 1980.
Experience: 7+ years of experience in biopharma, with a focus on clinical operations, R&D-related roles, regulatory affairs, project management, or cross-functional coordination
Salary: 141,928.00 USD - 171,979.00 USD
Type: Full time

Astrazeneca

HTA & Modelling Science Lead United States
Skills & Focus: HTA, Modelling, Statistical analysis, Data interpretation, Evidence synthesis, Comparative effectiveness, Indirect comparisons, Oncology, Meta-analysis, Health Economics
About the Company: AstraZeneca Spain is a rising force in our global business, with headquarters in Madrid and a global hub in Barcelona. We are committed to clinical development…
Experience: Prior experience working in consultancy or industry in applying expertise to support HTA submissions.
Type: Full time

Teleflex Incorporated

Clinical Trial Manager United States
Skills & Focus: clinical studies, data integrity, SOPs, monitoring visits, project management, risk mitigation, clinical evidence generation, medical technology, research experience, continuous improvement
About the Company: Teleflex is a global provider of medical technologies, driven by the purpose to improve health and quality of people’s lives. They offer a diverse portfolio wi…
Experience: Minimum eight years of clinical research experience, with at least two years managing direct reports.
Salary: $140,000 - $152,100
Type: Full-time
Benefits: Medical, prescription drug, dental and vision insurance, flexible spending accounts, participation in 401(k), various p…

Regeneron Pharmaceuticals

Associate Director, Field Medical Affairs (Gastroenterology/Rhinology) United States
Skills & Focus: Field Medical Affairs, Gastroenterology, Allergy, Rhinology, Clinical Research, Medical Specialists, Health Care Professionals, Scientific Expertise, Medical Strategy, Healthcare Trends
About the Company: Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or be…
Experience: Minimum of 5 years related work experience (clinical, managed care, or industry experience). Experience in a Field Medical Affairs position (Medical Science Liaison) is required.
Salary: $173,500.00 - $283,100.00
Type: Contract
Benefits: Health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off.

Cogent

Senior Manager/Associate Director of Regulatory Affairs United States
Skills & Focus: Regulatory Affairs, kinase inhibitors, oncology, rare diseases, regulatory strategies, cross-functional teams, strategic input, project teams, compliance, bio-pharmaceuticals
About the Company: A biopharmaceutical company focused on developing precision kinase inhibitors for oncology and rare diseases.
Experience: 5+ years in regulatory affairs, preferably in oncology or biopharmaceuticals.
Type: Full-time
Senior Manager/Associate Director of Regulatory Affairs United States
Skills & Focus: Regulatory Affairs, kinase inhibitors, oncology, rare diseases, regulatory strategies, cross-functional teams, strategic input, project teams, compliance, bio-pharmaceuticals
About the Company: A biopharmaceutical company focused on developing precision kinase inhibitors for oncology and rare diseases.
Experience: 5+ years in regulatory affairs, preferably in oncology or biopharmaceuticals.
Type: Full-time

Precision Medicine Group

Senior Manager Scientific Content United States
Skills & Focus: scientific marketing content, white papers, case studies, conference talks, webinars, content development, biomarker-driven development, drug development process, copywriting, scientific accuracy
About the Company: Precision Medicine Group provides services in support of preclinical and clinical development, including genomics and molecular assays, tissue and liquid biops…
Experience: Minimum of 10+ years of experience working in life sciences or relevant experience developing scientific content or as a copywriter, or PhD in life sciences plus 4+ years of experience working in life sciences
Salary: $120,400 – $180,600 USD
Type: Full-time
Benefits: Discretionary annual bonus, health insurance, retirement savings benefits, life insurance, disability benefits, parenta…

Amgen

Associate Director, Global Biomarker Lead – Oncology Clinical Biomarkers United States
Skills & Focus: biomarker research, oncology, clinical studies, biomarker strategies, pharmacodynamics, mechanisms of resistance, clinical protocols, team collaboration, biomarker platforms, clinical development
About the Company: 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…
Experience: Doctorate degree and 3 years of related clinical biomarker experience, or Master's degree and 5 years of related clinical biomarker experience, or Bachelor’s degree and 7 years of related clinical biomarker experience, or Associate’s degree and 12 years of related clinical biomarker experience, or High school diploma / GED and 14 years of related clinical biomarker experience.
Salary: 178,138.00 USD - 210,142.00 USD
Type: Full time
Benefits: A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions,…

Emergent Biosolutions

VP, Head of Clinical Development United States
Skills & Focus: clinical development, regulatory approval, clinical trials, product lifecycle management, cross-functional collaboration, data integrity, compliance, risk mitigation, global regulatory requirements, team leadership
About the Company: Emergent BioSolutions is involved in developing products designed to protect and enhance life, addressing public health challenges.
Experience: Minimum 15 years of experience in clinical development, including 5 years of progressive leadership experience managing clinical research teams and programs.
Salary: $291,000 to $352,200
Benefits: Emergent offers a comprehensive benefits package that includes eligibility for additional incentive compensation such a…

Biomérieux

Medical Science Liaison - Pacific Northwest United States
Skills & Focus: Medical Science Liaison, Infectious Diseases, Microbiology, Clinical Education, KOL Development, Healthcare Providers, Medical Engagement, Strategic Plan, Patient Care, Laboratory Innovation
About the Company: bioMĂ©rieux is a global company that provides diagnostic solutions for medical biology, including in vitro diagnostic products.
Experience: Minimum of 3 years of continuous significant clinical experience
Type: Full-time

Coherus Biosciences

Director, Thought Leader Strategy, I/O Commercial Franchise United States
Skills & Focus: pharmaceutical marketing, Thought Leader Development, KOL engagement, brand marketing, immuno-oncology, head and neck cancer, collaboration, project management, strategic thinking, insights generation
Experience: 2+ years of pharmaceutical marketing experience and Thought Leader Development experience
Salary: $190,000 - $240,000
Type: Exempt

Biomarin

Sr. Director, Clinical Supply Chain United States
Skills & Focus: clinical supply chain, vendor management, logistics, risk mitigation, supply planning, regulatory compliance, clinical trials, inventory management, cross-functional collaboration, strategic oversight
About the Company: BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future o…
Experience: Minimum of 15+ years of direct experience in clinical and commercial supply chain management
Salary: $211,200 to $316,800
Type: Full-time
Benefits: Benefits include company-sponsored medical, dental, vision, and life insurance plans, discretionary annual bonus, discr…

Apogee Therapeutics

Sr. Oversight Clinical Research Associate United States
Skills & Focus: clinical research, CRA, biotechnology, monitoring, clinical trials, data integrity, ICH guidelines, GCP, regulatory compliance, site management
About the Company: Apogee Therapeutics, Inc. is a biotechnology company seeking to develop differentiated biologics for the treatment of atopic dermatitis, chronic obstructive pu…
Experience: Minimum of 5 years of both monitoring experience and experience as a Sr. CRA/CRA from the biotechnology industry.
Salary: $120,000 - $150,000
Type: Full-time
Benefits: Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunit…

Medrio

Director of RTSM United States
Skills & Focus: RTSM, SaaS, clinical trials, life sciences, sales management, customer success, team leadership, healthcare solutions, software solutions, product strategy
About the Company: Medrio's SaaS offering is a key component in the pipeline of getting lifesaving drugs to the people who need them. We automate the clinic trial process and off…
Experience: Minimum 5 years successful RTSM leadership experience required
Salary: $175,000 - $200,000
Type: Full-time
Benefits: Medrio covers the cost of employee premiums for medical, dental, vision, life and LTD insurance, gym membership, and pr…
Director of RTSM United States
Skills & Focus: RTSM, SaaS, clinical trials, life sciences, sales management, customer success, team leadership, healthcare solutions, software solutions, product strategy
About the Company: Medrio's SaaS offering is a key component in the pipeline of getting lifesaving drugs to the people who need them. We automate the clinic trial process and off…
Experience: Minimum 5 years successful RTSM leadership experience required
Salary: $175,000 - $200,000
Type: Full-time
Benefits: Medrio covers the cost of employee premiums for medical, dental, vision, life and LTD insurance, gym membership, and pr…

Truveta

Senior Research Epidemiologist United States
Skills & Focus: Epidemiology, Research, Statistical programming, R, Python, Healthcare, Electronic Health Record data, Regulatory submissions, Pharmacoepidemiology, Collaboration
About the Company: Truveta is the world’s first health provider led data platform with a vision of Saving Lives with Data. Our mission is to enable researchers to find cures fast…
Experience: Minimum of 7 years with a Master's degree or 3 years with a PhD in Epidemiology.
Benefits: Great benefits package including strong medical, dental and vision insurance plans, 401K plan, professional development…