74 Clinical Data And Biostatistics jobs in Boston.

Hiring now: Exec Dir Biostatistics Ra @ Astrazenec, Dirsr Dir Clinical Data M @ Seaport Th, Sr Mgr Data Analytics And @ Johnson Jo, Dir Sports Epidemiology @ Iqvia, Dir Clinical Pharmacology @ Alexion, Associate Dir Of Clinical @ Tango Ther, Principal Scientist Neuro @ Regeneron , Scientist Ii Life Science @ Tempus, Dir Of Clinical Trial Man @ Formation , Sr Data Ops Analyst Healt @ Veeva Syst.Explore more at jobswithgpt.com.

🔥 Skills

clinical trials (20) project management (14) data analysis (14) regulatory submissions (10) clinical development (10) cross-functional collaboration (8) collaboration (7) Biostatistics (7) clinical research (7) biostatistics (6)

📍 Locations

Boston (48) Cambridge (25) Burlington (1)

Astrazeneca

Skills & Focus: biostatistics, pharmaceutical industry, clinical trials, leadership, statistical methodologies, regulatory submissions, collaboration, managerial experience, R&D strategies, communication skills
About the Company: A global, science-led biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines.
Experience: Managerial experience, background in clinical trials and/or pharmaceutical industry
Type: Full-time
Benefits: Inclusion and diversity initiatives, career development opportunities

Seaport Therapeutics

Skills & Focus: Clinical Data Management, Data Management SOPs, clinical trial objectives, data cleaning activities, compliance, regulatory requirements, electronic data capture, data quality, CDISC, project management
About the Company: Seaport Therapeutics is a clinical-stage biopharmaceutical company advancing the development of novel neuropsychiatric medicines in areas of high unmet patient…
Experience: 12+ years of data management experience or 14+ years with a Bachelor's degree

Johnson & Johnson

Skills & Focus: Data Analytics, Insights, Regulatory Affairs, Business Intelligence, Statistical Methods, SQL, Python, Data Visualization, Project Management, Data Integrity
About the Company: Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deli…
Experience: 8-10+ years of experience in Data analytics and/or Data Visualization
Type: Fully Remote

Iqvia

Skills & Focus: epidemiology, data science, sports injury, analytics, research, scientific leadership, team management, public health, program coordination, business development
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: 10 or more years of relevant experience for Master's degree; 7 or more years for Ph.D.
Salary: $177,800.00 - $330,200.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Alexion

Skills & Focus: clinical pharmacology, quantitative pharmacology, drug development, pharmacokinetics, pharmacodynamics, clinical trials, model-informed drug development, regulatory process, data analysis, team leadership
About the Company: AstraZeneca's Alexion division focuses on transforming the lives of people affected by rare diseases and devastating conditions through continuous innovation a…
Experience: At least 10 years of post-doctoral experience
Type: Full-time
Benefits: Tailored development programs, supportive community of leaders and peers, commitment to diversity and inclusion.

Tango Therapeutics

Skills & Focus: clinical data management, CROs, data handling, data management plans, database lock, clinical trials, CDASH, SDTM, vendor management, collaboration
About the Company: Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the trea…
Experience: At least 8 years of clinical data management experience in industry.

Astrazeneca

Skills & Focus: Clinical Safety, risk management, safety assessment, adverse event, signal detection, safety documents, medical review, epidemiological data, Patient Safety, Drug Development
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, dedicated to delivering life-changing medicines.
Experience: At least 2+ years of clinical experience post-registration
Salary: $233,290 to $349,935
Benefits: Qualifying retirement program (401(k) plan); paid vacation and holidays; paid leaves; health benefits including medical…

Tango Therapeutics

Skills & Focus: clinical trials, monitoring, oncology, data quality, ICH-GCP, site visits, enrollment, adverse events, collaboration, documentation
About the Company: Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the trea…
Experience: 6 years industry experience in clinical trials

Regeneron Pharmaceuticals Inc.

Skills & Focus: Principal Scientist, Neurology, Ophthalmology, Clinical Imaging, imaging biomarkers, neuroimaging, statistical analysis plans, imaging protocols, image analysis, clinical trials
Experience: PhD with 4+ years in Neurology and/or Ophthalmology Clinical Imaging
Salary: $126,700.00 - $206,900.00
Type: Contract
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off

Seaport Therapeutics

Skills & Focus: clinical studies, CRO management, Informed Consent Form, project leadership, timelines, budgets, site management, quality assurance, clinical trial communications, CNS therapeutic experience
About the Company: Seaport Therapeutics is a clinical-stage biopharmaceutical company advancing the development of novel neuropsychiatric medicines in areas of high unmet patient…
Experience: Minimum 4+ years of experience or demonstration of equivalent capability in a Clinical Trials Manager role
Type: Hybrid

Tempus

Skills & Focus: genomic sequencing, computational analysis, translational research, molecular data, multi-modal data, biopharmaceutical, scientific communication, clinical oncology, R programming, integrative modeling
About the Company: Tempus is a healthcare technology company at the forefront of change to leverage data to improve patient lives.
Experience: PhD or MSc with 4+ years of industry experience
Salary: $90,000 - $150,000 USD
Benefits: Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and o…

Formation Bio

Skills & Focus: clinical trial management, regulatory compliance, leadership, cross-functional collaboration, patient safety, data integrity, study design, biotechnology, strategic thinking, project management
About the Company: Formation Bio is a tech and AI driven pharma company differentiated by radically more efficient drug development. The company partners, acquires, or in-license…
Experience: Minimum of 10 years of experience in clinical trial management, with at least 5 years in a leadership role.
Salary: $211,000 - $250,000 (NYC Metro Area, Boston Metro Area, SF Bay Area) / $200,000 - $238,000 (All Other Eligible Remote Locations)
Type: Full-time
Benefits: Equity, generous perks, hybrid flexibility, and comprehensive benefits.

Astrazeneca

Skills & Focus: Director Clinical Scientist, Immunology, Cell Therapy, clinical trials, scientific leadership, data analysis, regulatory documents, clinical development, safety assessment, electronic data capture
About the Company: AstraZeneca is one of the world’s most forward-thinking and connected BioPharmaceutical companies, focused on delivering life-changing medicines.
Experience: 5 plus years of industry experience in clinical development

Iqvia

Skills & Focus: data management, clinical data management, project management, negotiations, quality management, financial tracking, process improvements, Good Clinical Practices, regulatory guidelines, compliance
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: 5 years direct Data Management experience, including 3 or more years as a CDM project lead.
Salary: $82,300.00 - $173,900.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs so you can thrive at work and at home.

Astrazeneca

Skills & Focus: epidemiology, pharmaceutical industry, strategic leadership, cross-functional collaboration, observational studies, data analysis, systematic literature reviews, study protocols, regulatory documents, project management
About the Company: AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development, and commercialization of prescription medicines, pri…
Experience: PhD/DSc/DrPH in Epidemiology with at least 6 years industry experience, or MPH/MSc in Epidemiology with at least 10 years industry experience
Type: Full-time

Tempus

Skills & Focus: biostatistics, epidemiology, computational biology, oncology, genomic data, data analysis, R, SQL, healthcare data, project management
About the Company: Tempus is on a mission to connect an entire ecosystem to redefine how genomic and clinical data is used for evidence-based medicine. They focus on precision me…
Experience: 1+ years of post-grad experience in computational biology, epidemiology, biostatistics, data science or related fields. 1+ post-grad experience with healthcare data.

Johnson & Johnson

Skills & Focus: Quantitative Sciences, Interventional Oncology, Data Analytics, Biostatistics, Statistical Methods, Drug Development, Regulatory Support, Statistical Communication, Collaboration, Mentorship
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: Ph.D. in Statistics or related field
Type: Hybrid

Alexion

Skills & Focus: epidemiology, pharmacoepidemiology, clinical development, patient safety, regulatory affairs, observational studies, data analysis, mentor, cross-functional teams, strategic planning
About the Company: At Alexion, we transform the lives of people affected by rare diseases and devastating conditions by continuously innovating and creating meaningful value in a…
Experience: PhD/DSc/DrPH in Epidemiology with at least 6 years industry experience in the pharmaceutical industry, biotechnology, or consulting environment, or MPH/MSc in Epidemiology with at least 10 years industry experience.

Tempus

Skills & Focus: Biostatistics, Epidemiology, Oncology, Cardiology, Statistical Analysis, Clinical Trials, Machine Learning, Regulatory Submissions, Data Analysis, Interdisciplinary Collaboration
About the Company: Tempus is building a business to develop, validate, and launch new predictive tests in oncology and new disease areas, leveraging clinical, molecular, and imag…
Experience: Ph.D. in Biostatistics, Statistics, or Epidemiology with a minimum of 3+ years of relevant experience, or equivalent with a Master’s.
Salary: $100,000 - $175,000 USD
Type: Full-time
Benefits: Tempus offers a full range of benefits which may include incentive compensation, restricted stock units, medical and ot…

Alexion

Skills & Focus: Neurology, genomic medicine, clinical development, protocol development, regulatory document, clinical trial, safety monitoring, medical content, business development, clinical research
About the Company: At Alexion, we’re inspired to think differently, to create better outcomes. By creating an unparalleled employee experience, our organization is equipped to ad…
Experience: MD, DO, MBBS (or equivalent) degree with relevant clinical specialty for the therapeutic area
Type: Hybrid

Veeva Systems

Skills & Focus: data management, MDM processes, data quality, health data terminology, data flows, cross-functional collaboration, data profiling, data validation, data modeling, analytics
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster.
Experience: 5+ years of data management/analysis experience
Salary: $80,000 - $145,000
Type: Full-time
Benefits: Medical, dental, vision, and basic life insurance; Flexible PTO; Retirement programs; 1% charitable giving program

Tango Therapeutics

Skills & Focus: statistical programming, clinical trials, SAS programming, data analysis, regulatory submissions, SDTM, ADaM, CRO management, biostatistics, programming standards
About the Company: Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the trea…
Experience: at least 8 years’ statistical programming experience

Kura Oncology

Skills & Focus: clinical development, oncology studies, drug discovery, clinical research, medical monitor, regulatory deliverables, precision oncology, team leadership, strategic execution, data analysis
About the Company: Kura Oncology is a clinical-stage biopharmaceutical company discovering and developing personalized therapeutics for the treatment of blood cancers and solid t…
Experience: Minimum of 3 years of relevant experience in drug development either in industry (preferred) or in academia.
Salary: $318,000 to $364,000
Type: Full-time
Benefits: Generous benefits package including 401K, PTO, maternity/paternity leave, catered lunches, and equity.

Costello Medical

Skills & Focus: Medical Communications, Evidence Development, Value and Access, scientific data, clinical trials, data presentation, medical education, systematic searches, clinical trial manuscripts, HTA submissions
About the Company: Fast-growing healthcare consultancy that works with a variety of clients including pharmaceutical and medical technology companies, patient and public health o…
Experience: Recent graduates and post-graduates, as well as current students permitted to complete full-time internships.
Salary: $24 to $30 per hour
Type: Full-time, 3-month internship
Benefits: Generous vacation leave allowance, flexible working hours, the chance to work from home 1 day per week, access to medic…

Alexion

Skills & Focus: epidemiology, clinical development, strategic plan, data analysis, observational studies, disease registries, cross-functional teams, project management, mentoring, regulatory affairs
About the Company: To transform the lives of people affected by rare diseases and devastating conditions by continuously innovating and creating meaningful value in all that we d…
Experience: PhD / DSc / DrPH in Epidemiology with at least 6 years industry experience or MPH/MSc in Epidemiology with at least 10 years industry experience.
Type: Full-time

Tango Therapeutics

Skills & Focus: biostatistics, clinical trials, statistical modeling, regulatory submissions, oncology, FDA, SAS, R, statistical analysis plans, data standards
About the Company: Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the trea…
Experience: At least 12 years’ experience in the pharmaceutical or biotech industry

Boston Scientific

Skills & Focus: clinical trial, protocol development, regulatory submissions, data analysis, clinical strategy, evidence strategy, medical device, Good Clinical Practices, statistical analysis, cross-functional collaboration
About the Company: A leader in medical science for over 40 years, Boston Scientific is committed to solving the challenges that matter most in healthcare, united by a deep caring…
Experience: Minimum 10 years of medical device clinical trial experience
Salary: $127900 - $243000
Type: Hybrid
Benefits: Core and optional employee benefits; details available at www.bscbenefitsconnect.com

Iqvia

Skills & Focus: data management, leadership, project planning, execution, customer satisfaction, collaboration, healthcare, clinical data, quality deliverables, innovation
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: 5-7 years direct Data Management experience, including experience as a CDM project lead.
Salary: $82,300.00 - $173,900.00
Type: Full time
Benefits: Work/life balance, flexible schedules, strong team environment, technical training, career advancement opportunities.

Orchard Therapeutics

Skills & Focus: clinical trials, clinical study, administration, project support, documentation, communication, organisational skills, study trackers, CRO, finance reconciliation
About the Company: Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the develop…
Experience: 2-years CTA experience; Experience & knowledge of supporting clinical trials, particularly coordination/administration

Costello Medical

Skills & Focus: clinical data analysis, scientific writing, medical communications, market access, evidence development, publications, regulatory documents, healthcare, patient access, creative presentation skills
About the Company: Costello Medical is structured into divisional teams focusing on distinct services within the healthcare industry. The company has a presence in the US (Boston…
Experience: Recent graduates in the sciences; those with experience in scientific research
Salary: $70,000 to $73,000 per annum
Type: Full-time, Permanent
Benefits: Hybrid working options, generous holiday allowance, flexible working hours, private medical and dental insurance, 401K …

Formation Bio

Skills & Focus: medical writing, clinical development, regulatory documents, pharmacovigilance, cross-functional teams, AI tools, Good Clinical Practice, document author, stylish guidelines, continuous improvement
About the Company: Formation Bio is a tech and AI driven pharma company focused on radically more efficient drug development, utilizing technology platforms and AI advancements t…
Experience: 7+ years in the development of clinical and regulatory documents
Salary: $250,000 - $300,000 for NYC and Boston; $238,000 - $285,000 for other eligible remote locations
Type: Hybrid
Benefits: Equity, generous perks, hybrid flexibility, comprehensive benefits

Iqvia

Skills & Focus: monitoring, site management, Good Clinical Practice, study protocol, subject recruitment, documentation, data integrity, communication, regulatory submissions, clinical trial
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: Requires at least 2 years of on-site monitoring experience.
Salary: $71,900.00 - $189,000.00
Type: Full time
Benefits: Benefits programs are designed to meet your total well-being needs.

Om1

Skills & Focus: Epidemiology, Pharmacoepidemiologic studies, Healthcare datasets, Clinical research, Data collection, Study design, Regulatory environment, Analytic services, Leadership, Mentoring
About the Company: OM1 is a healthcare data and technology company focused on real world clinical data and outcomes, accelerating medical research and personalizing healthcare.
Experience: Deep experience with the design, conduct, and interpretation of pharmacoepidemiologic studies.
Benefits: Growth, learning opportunities, and achievement for every employee.

Atalanta Therapeutics

Skills & Focus: nonclinical safety programs, GLP, toxicology, safety assessments, regulatory submissions, CRO management, study design, FDA guidance, Good Laboratory Practices, data-driven decisions
About the Company: Atalanta Therapeutics is developing novel Di-siRNA therapies to treat severe neurological diseases at the root cause, building on the founders’ Nobel-prize win…
Experience: 8-10 years in toxicology, pharmacology, or related discipline
Type: Full-time

Pa Health Data Platforms

Skills & Focus: Clinical Data Management, EHR, Data Integrity, Data Quality, Standards Compliance, Customer Support, Documentation, Data Processing, Collaboration, Analytics

Veeva Systems

Skills & Focus: Pharmacovigilance, Drug Safety, Reporting, Analytics, Vault Safety, Implementation, SQL, Data Analysis, Client Engagement, Compliance
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: 5+ years of experience in Drug Safety, Pharmacovigilance, Healthcare, or adjacent Safety Industry, with at least 2 years of experience in leading PV reporting workstreams
Salary: $80,000 - $200,000
Type: Full-time
Benefits: Medical, dental, vision, and basic life insurance; Flexible PTO and company paid holidays; Retirement programs; 1% char…

Om1

Skills & Focus: real world data, epidemiology, study design, analytic approaches, dissemination of findings, biopharmaceutical product life cycle, data analytic, research questions, subject matter expertise, prospective study designs
About the Company: OM1 is a healthcare data and technology company focused on real world clinical data and outcomes, accelerating medical research and personalizing healthcare.

Veeva Systems

Skills & Focus: Pharmacovigilance, SaaS, Software Product Strategy, Safety Suite, market adoption, data collection, data processing, data analysis, process management, regulatory compliance
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Experience: Deep understanding of the Pharmacovigilance function and related business processes
Type: Full-time
Benefits: Work Anywhere policy, flexibility to work from home or in the office

Precision Medicine Group

Skills & Focus: Health Economics, Outcome Research, Statistical Analysis, Cost-effectiveness Models, Budget Impact Models, Microsoft Excel, VBA, SAS, Team Collaboration, Research Communication
About the Company: Precision Medicine Group is an established global portfolio organization focusing on health economics and outcomes research (HEOR). Our culture is similar to t…
Experience: 2-5 years' relevant research experience
Salary: $84,000 - $117,000 USD
Benefits: Discretionary annual bonus, health insurance, retirement savings benefits, life insurance, disability benefits, parenta…

Veeva Systems

Skills & Focus: Master Data Management, data products, data quality, data consistency, data standardization, Terminology Reference Library, health data terminologies, data domains, data flows, continuous improvement
About the Company: Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the…
Benefits: flexibility to work from home or in the office

Nchroma Bio

Skills & Focus: clinical trial, stakeholder management, CRO oversight, GCP, ICH guidelines, clinical trial methodology, budget management, risk management, cross-functional team, vendor management
About the Company: nChroma Bio is a pioneering biotechnology company redefining the future of in vivo targeted genetic medicine to treat a wide array of diseases and bring cures …
Experience: 8+ years
Type: Full-time

Boston Scientific

Skills & Focus: Clinical Data, eCRF Design, Data Management, Collaboration, Medical Device, Data Integrity, Validation, Technical Design, Good Clinical Practices, User Acceptance Testing
About the Company: Boston Scientific is a leader in medical science for more than 40 years, committed to solving the challenges that matter most, united by a deep caring for huma…
Experience: Minimum 2 years of Clinical Database (eCRF) Design experience
Salary: $76,000 - $144,400
Type: Hybrid
Benefits: Competitive core and optional employee benefits

Sophia Genetics

Skills & Focus: Companion Diagnostics, Clinical Trial Assays, Regulatory Affairs, Oncology, Rare Diseases, CDx collaborations, IVD, Regulatory submissions, NGS, BioPharma partnerships
About the Company: SOPHiA GENETICS is focused on BioPharma solutions, providing access to high-quality NGS solutions through their patented SOPHiA DDM™ platform, including ctDNA-…
Experience: 10+ years of Regulatory Affairs experience in the pharmaceutical or diagnostics industry, including 5+ years in IVD.
Type: Permanent
Benefits: Comprehensive US benefits package including medical (with telemedicine), dental and vision plans, life and AD&D insuran…

Costello Medical

Skills & Focus: health economic models, stakeholder communication, resource allocation, strategic advice, project management, client relationships, economic modelling techniques, healthcare interventions, pharmaceutical companies, data analysis
About the Company: Costello Medical is a rapidly growing global healthcare agency specialising in medical communications, market access and health economic and outcomes research.…
Experience: Minimum of 2 years in health economics, economic or mathematical modelling techniques, ideally in a pharmaceutical or medical consulting environment
Salary: $95,000 to $102,000 per annum
Type: Full-time, permanent
Benefits: Discretionary profit share bonuses, hybrid and flexible working options, generous vacation allowance, private medical a…

Orchard Therapeutics

Skills & Focus: clinical trials, administration, clinical operations, project management, study trackers, timelines, collaboration, regulatory affairs, communication, organization
About the Company: Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the develop…
Experience: 2-years CTA experience

Johnson & Johnson

Skills & Focus: clinical trials, oncology, medical monitoring, protocol development, clinical research, solid tumors, data management, regulatory affairs, biostatistics, cross-functional teams
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: 3 or more years in clinical research within the pharmaceutical industry or academia
Type: Hybrid

Tempus

Skills & Focus: clinical development, precision medicine, genomics, genomic assays, AI, clinical trials, bioinformatics, medical monitoring, collaborations, clinical research
About the Company: Tempus' proprietary platform connects an entire ecosystem of real-world evidence to deliver real-time, actionable insights to physicians, providing critical in…
Experience: 7+ years of clinical research experience
Salary: $315,000 — $360,000 USD
Benefits: Tempus offers a full range of benefits, which may include incentive compensation, restricted stock units, medical and o…

Pa Health Data Platforms

Skills & Focus: Clinical Data Management, EHR systems, Data Integrity, Standards Compliance, LOINC, FHIR, HL7, ICD-10, Data Quality Assurance, Documentation and Reporting
About the Company: A team focused on delivering software data services by analyzing and processing clinical data.
Experience: Extensive experience with clinical data from Electronic Health Records (EHRs) and other clinical systems

Boston Scientific

Skills & Focus: Clinical Data, eCRF Design, Data Management, Collaboration, Medical Device, Data Integrity, Validation, Technical Design, Good Clinical Practices, User Acceptance Testing
About the Company: Boston Scientific is a leader in medical science for more than 40 years, committed to solving the challenges that matter most, united by a deep caring for huma…
Experience: Minimum 2 years of Clinical Database (eCRF) Design experience
Salary: $76,000 - $144,400
Type: Hybrid
Benefits: Competitive core and optional employee benefits

Aditum Bio

Skills & Focus: Biostatistics, clinical trials, statistical design, data analysis, regulatory compliance, Neuroscience, Immunology, statistical software, collaboration, adaptive designs
About the Company: At Aditum Bio our mission is to provide access to medicines to patients in need. Co-founded by industry veterans Joe Jimenez, former CEO of Novartis and Mark F…
Experience: At least 8 years of biopharma experience, with a track record in clinical trial design and analysis, ideally in agile biotech environments.
Salary: $225,000 - $250,000
Type: Full-time
Benefits: Target bonus, equity compensation and benefits including medical, dental, vision, and 401k.

Iterative Health

Skills & Focus: clinical research, regulatory compliance, Phase 2-4 clinical trials, Good Clinical Practice (GCP), FDA guidelines, project management, organizational skills, communication skills, clinical trial management, Adobe Pro
About the Company: Iterative Health is a healthcare technology and services company on a mission to advance gastrointestinal care through relentless innovation. With deep experti…
Experience: 5+ years of relevant work experience
Salary: $85,000 — $100,000 USD
Type: Full-time
Benefits: Vision/Dental/Medical Insurance, Life/Disability Insurance, Parental Leave, Stock Options, Flexible Work Hours, Unlimit…

Johnson & Johnson

Skills & Focus: clinical research, medical and scientific contribution, clinical development strategy, regulatory affairs, clinical operations, health authorities, clinical study reports, interpersonal skills, problem-solving skills, Ophthalmology
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: At least 7 years of experience in clinical research and development.
Salary: $226,000 to $391,000 USD
Type: Hybrid Work
Benefits: Employees may be eligible to participate in Company employee benefit programs such as health insurance, savings plan, p…

Beam Therapeutics

Skills & Focus: pharmacovigilance, safety reports, clinical trials, signal detection, risk management, MedDRA dictionary, aggregate safety reports, electronic data capture, FDA regulations, project management
About the Company: Beam Therapeutics is committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembl…
Experience: 10+ years’ pharmaceutical industry experience, including a minimum of 5 years’ experience in pharmacovigilance (PV).

Regeneron Pharmaceuticals Inc.

Skills & Focus: clinical trials, study design, project management, regulatory guidelines, budget management, cross-functional leadership, data management, risk assessment, site evaluation, clinical study delivery
About the Company: Regeneron is an equal opportunity employer and has an inclusive and diverse culture that provides comprehensive benefits.
Experience: minimum of 8 years of relevant industry experience
Salary: $148,300.00 - $241,900.00
Type: Full-time
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off

Parexel

Skills & Focus: Clinical Logistics, Remote, Clinical Trials, Project Leader, Biostatistics, Clinical Research, Data Management, Medical Writing, Functional Service Provider, Supply Chain

Biogen

Skills & Focus: medical leadership, clinical programs, translational programs, rare diseases, clinical study design, data interpretation, multidisciplinary team, research-to-development, strategic initiatives, collaboration

Beam Therapeutics

Skills & Focus: clinical development, medical monitoring, gene therapies, sickle cell disease, beta-thalassemia, Target Product Profile, Clinical Development Plan, Good Clinical Practices, regulatory submissions, collaborations with study investigators
About the Company: Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this …
Experience: 15+ years

Blueprint Medicines

Skills & Focus: Medical Safety Lead, Pharmacovigilance, Clinical Trials, Risk Management, Safety Data, Safety Signals, Aggregate Reports, Drug Safety Regulations, Cross-functional Collaboration, Subject Matter Expert
About the Company: Blueprint Medicines is a global, fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solvi…
Experience: 6+ years’ experience as a Medical Safety Lead/Global Safety Officer in clinical trials in the pharmaceutical industry.
Type: Full-time

Amylyx Pharmaceuticals

Skills & Focus: clinical development, strategic leadership, clinical trial design, regulatory engagement, stakeholder collaboration, budget management, cross-functional teams, clinical data analysis, rare disease drug development, communication skills
About the Company: Amylyx is a pharmaceutical company based in Cambridge, Massachusetts, dedicated to the discovery and development of potential treatments for neurodegenerative …
Experience: Minimum of 15 years in clinical development within the biotechnology or pharmaceutical industry, with significant experience leading teams in rare disease drug development.
Type: Remote

Regeneron

Skills & Focus: clinical trials, project management, study design, budget management, stakeholder engagement, risk mitigation, data quality, clinical operations, protocol development, vendor management
Experience: Minimum of 8 years of relevant industry experience.
Salary: $145,400.00 - $237,200.00
Type: Contract
Benefits: health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off.

Iterative Health

Skills & Focus: data annotation, machine learning, cross-functional, project management, annotation teams, clinical research, regulatory submissions, quality metrics, dynamically-paced environment, Gastroenterology
About the Company: Iterative Health is a healthcare technology and services company on a mission to advance gastrointestinal care through relentless innovation. With deep experti…
Experience: Over 2 years of experience in data annotation, data operations, or related fields, including at least 1 year in leading annotation teams.
Benefits: Vision/Dental/Medical Insurance, Life/Disability Insurance, Parental Leave, Stock Options, Flexible Work Hours, Unlimit…

Blueprint Medicines

Skills & Focus: medical writing, regulatory submissions, clinical data, cross-functional collaboration, document management, project management, regulatory compliance, Common Technical Document, quality control, standard operating procedures
About the Company: Blueprint Medicines is a global, fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solvi…
Experience: 7+ years of experience in medical/clinical/regulatory writing in the pharmaceutical/biotechnology/healthcare industry; 3+ years of regulatory document project management oversight/experience

Amylyx Pharmaceuticals

Skills & Focus: clinical trials, clinical development, medical monitoring, clinical study design, data interpretation, regulatory documents, neurodegenerative diseases, rare diseases, leadership, interpersonal skills
About the Company: A clinical-stage pharmaceutical company based in Cambridge, Massachusetts, focused on developing novel therapies for high unmet needs.
Experience: 8+ years of experience in leading clinical development programs in the biotechnology/pharmaceutical industry
Type: Remote friendly

Blueprint Medicines

Skills & Focus: statistical programming, CDISC datasets, SDTM, ADaM, clinical studies, R, SAS, communication skills, biostatistics, internship program
About the Company: Blueprint Medicines is a global, fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solvi…
Experience: Currently enrolled in a Master program for Computer Science, Pharmacy, Mathematics, Statistics or Biostatistics with a minimum of one year graduate school completed.
Salary: $23.00-$25.00 per hour
Type: Internship
Benefits: Summer Internship Program includes mentoring, networking events, lunch and learn sessions, and volunteer opportunities.…
Skills & Focus: Medical Safety, Drug Safety, Pharmacovigilance, Safety Surveillance, Risk Management, Clinical Trials, Safety Reports, ICSRs, Regulatory Filings, Mentorship
About the Company: Blueprint Medicines is a global, fully integrated biopharmaceutical company that invents life-changing medicines. We seek to alleviate human suffering by solvi…
Experience: 3+ years of experience as a product safety lead in Drug Safety/Pharmacovigilance in a pharmaceutical or biotech company, CRO, or regulatory agency.

Biogen

Skills & Focus: clinical trials, site management, local operational expertise, patient safety, investigator relationships, regulatory compliance, cross-functional collaboration, clinical development strategy, KPI monitoring, operational direction
About the Company: Biogen is a biotechnology company specializing in the discovery, development, and delivery of innovative therapies for the treatment of neurological diseases.
Experience: Experienced research professional with site management experience.
Type: Full-time

Boston Scientific

Skills & Focus: clinical trial, protocol development, regulatory submissions, data analysis, clinical strategy, evidence strategy, medical device, Good Clinical Practices, statistical analysis, cross-functional collaboration
About the Company: A leader in medical science for over 40 years, Boston Scientific is committed to solving the challenges that matter most in healthcare, united by a deep caring…
Experience: Minimum 10 years of medical device clinical trial experience
Salary: $127900 - $243000
Type: Hybrid
Benefits: Core and optional employee benefits; details available at www.bscbenefitsconnect.com

Amgen

Skills & Focus: data analytics, statistical process control, multivariate statistical analysis, visualizations, regulatory report authoring, data scientists, process engineers, cGMP activities, analytical method development, innovation
About the Company: Amgen is a leading biotech company that pioneers innovative treatments for serious illnesses. The company focuses on four therapeutic areas: Oncology, Inflamma…
Experience: 10 years of data analytics experience OR Associate’s degree and 8 years of data analytics experience OR Bachelor’s degree and 4 years of data analytics experience OR Master’s degree and 2 years of data analytics experience OR Doctorate degree
Salary: 137,855.00 USD - 168,574.00 USD
Type: Flex Commuter / Hybrid
Benefits: Comprehensive employee benefits package, including health and welfare plans, total rewards plan, retirement savings pla…

Biogen

Skills & Focus: Safety, Analytics, Pharmacovigilance, Regulatory, Software Implementations, Technology Strategy, Database Design, Reports Migration, Validation Strategy, Process Optimization

Regeneron Pharmaceuticals Inc.

Skills & Focus: Biostatistics, clinical trials, drug development, statistical methodology, cross-functional collaboration, data analysis, regulatory interactions, training, process improvement, leadership
About the Company: Regeneron is a biotechnology company that invents life-transforming medicines for people with serious diseases.
Experience: >6 years (PhD) or >11 years (MS) in the pharmaceutical industry
Salary: $170,100.00 - $277,500.00
Type: Contract
Benefits: comprehensive benefits including health and wellness programs, fitness centers, equity awards, annual bonuses, and paid…

Regeneron

Skills & Focus: Bioinformatics, Data Scientist, human genetics, Cardiovascular, Metabolic, Musculoskeletal, analytical methods, genetic analyses, high-performance computing, statistics
About the Company: Regeneron specializes in discovering new disease biology and highlighting drug targets using extensive human genetic datasets.
Experience: At least 3 years of relevant post-doc experience
Salary: $173,500.00 - $283,100.00
Type: Contract
Benefits: Comprehensive benefits including health programs, fitness centers, equity awards, annual bonuses, and paid time off.

Moma Therapeutics

Skills & Focus: Regulatory Affairs, FDA interactions, Drug development, Oncology programs, Regulatory submissions, Clinical trials, Team leadership, Biopharmaceutical industry, Companion Diagnostics, Regulatory strategy
About the Company: MOMA Therapeutics is a clinical-stage, next-generation precision medicine company dedicated to targeting highly dynamic proteins that underlie human disease vi…
Experience: A minimum of 9 years of Regulatory Affairs experience in the biopharmaceutical industry with at least 3 years of Regulatory experience with oncology programs.
Type: Full-time
Benefits: Competitive benefits package including health, dental and vision coverage, unlimited PTO, week-long company shutdown, c…

Parexel

Skills & Focus: Clinical Research, Biostatistics, Data Management, Project Leadership, Quality Assurance, Clinical Trials, Remote Work, Functional Service Provider, Statistical Programming, Health Economics
About the Company: Parexel is a global clinical research organization that provides a range of services to the biopharmaceutical industry, helping clients bring new therapies to …
Skills & Focus: Medical Writing, Clinical Research, Regulatory Affairs, Biostatistics, Data Management, Healthcare, Pharmaceuticals, FSP, Clinical Trials, Technical Editing
About the Company: Parexel provides innovative drug development and regulatory consulting services to the global biopharmaceutical industry.
Type: Remote