44 Clinical Data And Biostatistics jobs in Remote - United States.

Hiring now: Solution Consultant Assoc @ Parexel, Staff Medical Science Lia @ Guardanthe, Dir Statistical Programmi @ Arcus Bios, Coding Quality Auditor @ Conifer He, Global Pharmacovigilance @ Amgen, Clinical Study Monitor Co @ Natera, Medical Monitor @ Psi, Sr Quantitative Scientist @ Verana Hea, Medical Writer Consultant @ Iqvia, Associate Clinical Resear @ Novartis.Explore more at jobswithgpt.com.

🔥 Skills

clinical trials (9) regulatory compliance (6) clinical studies (6) clinical research (5) Medical Writing (4) project management (4) biostatistics (4) oncology (4) clinical development plans (4) risk mitigation (4)

đź“Ť Locations

United States (44)
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Parexel

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
Study Operations Manager I United States
Skills & Focus: study management, clinical trials, vendor management, recruitment strategy, project management, regulatory compliance, clinical research, site activation, risk management, communication
About the Company: Parexel is a global clinical research organization that provides drug development and regulatory consulting services.
Experience: Minimum of 5 years of relevant global/regional clinical trial management experience.
Type: Full-time
Lead Clinical Research Associate - Oncology United States
Skills & Focus: Clinical Trials, CRA, Functional Service Provider, Oncology, Site Care Partner, Remote, Biostatistics, Data Management, Medical Writing, Regulatory Affairs

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

Conifer Health Solutions

Coding Quality Auditor United States
Skills & Focus: coding, data quality audits, ICD-9-CM, CPT-4, medical records, discharge disposition, standards of ethical coding, consulting, chart analysis, professional development
About the Company: Conifer Health brings 30 years of healthcare industry expertise to clients in more than 135 local regions nationwide.
Experience: Three years coding experience including hospital and consulting background
Salary: $30.85 - $46.28 per hour
Type: Full-time
Benefits: Medical, dental, vision, disability, and life insurance, Paid time off (vacation & sick leave), 401k with up to 6% empl…

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.

Natera

Clinical Study Monitor - Companion Diagnostics (CDx) United States
Skills & Focus: Clinical Study Monitor, companion diagnostics, clinical studies, IVDR, GCP, FDA regulations, monitoring, data quality, diagnostic laboratory, protocol deviations
About the Company: Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic t…
Experience: 3–5 years in clinical research, with at least 2 years in monitoring IVD or CDx studies.
Salary: $98,400 - $123,000 USD
Type: Full-time
Benefits: Employee benefits include comprehensive medical, dental, vision, life and disability plans, free testing for employees …

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…

Verana Health

Senior Quantitative Scientist United States
Skills & Focus: biostatistics, epidemiology, observational data, health data analytics, commercial projects, clinical development cycle, statistical analysis plans, collaborating with life science companies, cross-functional teams, real-world data
About the Company: a digital health company that delivers quality drug lifecycle and medical practice insights from an exclusive real-world data network
Experience: 5+ years of hands-on experience with messy data and analytical methodologies; 5+ years working with life science/pharmaceutical/biotechnology organizations
Salary: $150,000 — $175,000 USD
Type: Full-time
Benefits: We provide health, vision, and dental coverage for employees; 401k Match - 3% match paid year end, up to $1000/year; A …
Senior Quantitative Scientist United States
Skills & Focus: biostatistics, epidemiology, observational data, health data analytics, commercial projects, clinical development cycle, statistical analysis plans, collaborating with life science companies, cross-functional teams, real-world data
About the Company: a digital health company that delivers quality drug lifecycle and medical practice insights from an exclusive real-world data network
Experience: 5+ years of hands-on experience with messy data and analytical methodologies; 5+ years working with life science/pharmaceutical/biotechnology organizations
Salary: $150,000 — $175,000 USD
Type: Full-time
Benefits: We provide health, vision, and dental coverage for employees; 401k Match - 3% match paid year end, up to $1000/year; A …

Amgen

Clinical Systems & Analytical Reporting Manager United States
Skills & Focus: clinical application technologies, stakeholders, technology implementation, clinical trial execution, business requirements, integration specifications, documentation, audit findings, clinical research, biopharmaceutical development
About the Company: Amgen is a biotechnology company that focuses on pioneering innovative medicines to serve patients with serious illnesses since 1980.
Experience: Doctorate Degree or Master's Degree and 3 years of clinical experience or Bachelor's Degree and 5 years of clinical experience or Associates degree and 10 years of clinical experience or High school diploma/GED & 12 years of clinical experience
Salary: 130,065.00 USD - 155,856.00 USD
Type: Full-time

Iqvia

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.
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.

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…

Iqvia

Clinical Trial Assistant United States
Skills & Focus: Clinical Trial Assistant, administrative activities, Trial Master File, Clinical Research Associates, document maintenance, regulatory compliance, clinical documents, Case Report Forms, clinical monitoring, Microsoft Office
About the Company: IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industri…
Experience: 3 years administrative support experience.
Salary: $42,800.00 - $95,000.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Novartis

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

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…

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…

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.

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…

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

Biogen

Senior Clinical Trial Specialist United States
Skills & Focus: clinical trials, GCP, SOPs, administration, coordination, organizational support, protocol review, study management, inspection readiness, supplier management
About the Company: Biogen’s West Coast Hub, based in South San Francisco, is specifically focused on transforming the lives of patients with severe immune-mediated diseases by de…

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

Verana Health

Quantitative Scientist United States
Skills & Focus: biostatistics, epidemiology, data science, real-world data, clinical studies, cross-functional, SQL, Python, R, clinical datasets
About the Company: A digital health company that delivers quality drug lifecycle and medical practice insights from an exclusive real-world data network.
Experience: 3+ years of hands-on experience with messy data and analytical methodologies; 1+ years working with life science/pharmaceutical/biotechnology organizations.
Salary: $130,000 - $165,000 USD
Benefits: 100% health, vision, and dental coverage, 401K Match, flexible vacation plans, $700 learning and wellness annual stipen…

Natera

Clinical Biospecimen Operations Manager United States
Skills & Focus: clinical research, biospecimen management, project management, regulatory compliance, clinical protocols, sample processing, data management, KPI reporting, clinical trial supplies, SOPs
About the Company: Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic t…
Experience: Minimum of 5 years of experience working on clinical studies in the academic, biopharma, diagnostics, or medical device fields
Salary: $111,900 - $139,900 USD
Type: Full-time
Benefits: Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and t…

Iodine Software

Clinical Product Consultant - CDI United States
Skills & Focus: CDI, implementation, client success, healthcare, clinical, AI technology, data analysis, best practices, product development, patient care
About the Company: Iodine is an enterprise AI company that is championing a radical rethink of how to create value for healthcare through technology.
Experience: 5-7 years in CDI role
Salary: $120K – $145K
Type: Full time
Benefits: Comprehensive Healthcare, Telehealth Services, Savings Accounts, Ancillary Benefits, Retirement Plan, Extra Life Insura…

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…

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…

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

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…

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…

Q-Centrix

VQI Data Abstractor United States
Skills & Focus: Vascular Quality Initiative, Data Abstractor, Carotid Artery Stent, Carotid Endarterectomy, Endovascular AAA Repair, Open AAA Repair, Hemodialysis Access, Peripheral Vascular Intervention, Thoracic and Complex EVAR, Varicose Vein
Experience: Experience abstracting for the Vascular Quality Initiative (VQI) in the last 12 months.
Type: Part-time

Regeneron Pharmaceuticals Inc.

Senior Manager, Clinical Publications Writer United States
Skills & Focus: clinical, publications, medical writing, scientific writing, abstracts, manuscripts, project management, oncology, hematology, publication strategy
Experience: Over 3 years scientific and clinical writing of journal articles from a biopharma and/or medical communications agency
Salary: $132,400.00 - $216,000.00
Type: Contract
Benefits: Health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees

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…

Syneos Health

Principal/Sr Medical Writer (CMH Publications) United States
Skills & Focus: medical writing, clinical study protocols, clinical study reports, IND submissions, NDA submissions, clinical development plans, regulatory standards, peer reviewer, presentation skills, leadership skills
About the Company: Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medic…
Salary: $85,500.00 - $175,700.00
Benefits: Health benefits to include Medical, Dental and Vision, Company match 401k, eligibility to participate in Employee Stock…

Biogen

Medical Director, Global Medical Safety United States
Skills & Focus: pharmacovigilance, safety data analysis, adverse events, clinical development, strategic leadership, safety surveillance, Regulatory compliance, Clinical Operations, safety reports, benefit-risk profile
About the Company: Biogen is a biotechnology company that develops therapies for neurological and neurodegenerative diseases.
Experience: Experience in pharmacovigilance and safety data analysis.
Type: Full-time
Medical Director, Global Medical Safety United States
Skills & Focus: pharmacovigilance, safety data analysis, adverse events, clinical development, strategic leadership, safety surveillance, Regulatory compliance, Clinical Operations, safety reports, benefit-risk profile
About the Company: Biogen is a biotechnology company that develops therapies for neurological and neurodegenerative diseases.
Experience: Experience in pharmacovigilance and safety data analysis.
Type: Full-time

Astrazeneca

Senior Statistician II United States
Skills & Focus: Statistical Analysis Plan, preclinical studies, clinical programmes, regulatory submissions, modeling and simulation, statistical methodology, quality improvement, data transformation, team collaboration, pharmaceutical industry
About the Company: AstraZeneca Spain is a rising force in our global business. With headquarters in Madrid and our global hub in Barcelona, we’ve become an important internationa…
Experience: MSc/PhD in Statistics, Mathematics (containing a substantial statistical component), or recognized equivalent to stats MSc. Experience of design, analysis, and reporting of preclinical or clinical studies in more than one setting.
Type: Full time