24 lead clinical data manager jobs at 18 companies in Salem, MA
3mo
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Senior Clinical Data Manager
Cambridge, Massachusetts, United States
$131k-$187k/yr OnsiteFull Time
7+ YOE7+ years in industry-sponsored clinical trials; lead data management; oversee CROs/vendors; Medidata Rave experience; CDISC/CDASH/SDTM/ADaM knowledge; oncology trial experience.
Medidata Rave, eCRF, CDASH, SDTM, ADaM
1w
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Senior Manager, Clinical Data Management
Burlington or Carmel
OnsiteFull Time
9+ YOEMaster’s degree in a relevant field and 9+ years of clinical data management experience in biotech, pharmaceutical, or CRO settings, including global Phase 2/3 lead data management.
Medidata Rave, EDC, eCOA, eDiary, IRT, TMF
1mo
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Director, Clinical Data & AI
Andover or Mansfield or Fort Worth or Pittsburgh or Memphis or Austin
$165k-$236k/yr HybridFull Time
10+ YOE10+ years clinical data/AI/platform leadership in medtech/pharma/biotech; experience with enterprise data architecture, regulatory submissions, and leading multi-domain teams; Databricks preferred.
Databricks, EDC, eCOA, Clinical Data Lake, CDISC, ADaM, TFLs
1w
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Associate Director, Clinical Data Management
Boston, Massachusetts, United States
$175k-$200k/yr HybridFull Time
8+ YOE3+ MgmtRequires 8+ years of clinical data management experience and 3+ years leading data management and vendor relationships in biotechnology, pharmaceutical, or CRO environments, including Phase 2/3 and regulatory submissions.
Good Clinical Practice (GCP), ICH guidelines, FDA, EMA, CDISC, SDTM
1w
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Clinical Operations Lead
Boston, Massachusetts, United States
HybridFull Time
3+ YOEActive Massachusetts RN or NP license, 3+ years of clinical experience with patient-facing care, and 1+ year in digital health or software product teams. Epic EHR experience and clinical data expertise preferred.
Epic, Electronic Health Record (EHR), Electronic Medical Record (EMR)
3d
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Global Clinical Program Lead
Boston, Massachusetts, United States
$288k-$432k/yr HybridFull Time
5+ YOEM.D., Ph.D., or equivalent qualification; 5–8 years of clinical development experience, including trial design, implementation, monitoring, data interpretation, and reporting; expertise in safety, GCP, regulatory requirements, and cross-functional leadership.
1mo
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Director, Clinical Development Scientist (Non-MD)
Collegeville or La Jolla or Lake Forest or Cambridge or Groton or New York City
$177k-$294k/yr HybridFull Time
5+ YOELead clinical execution, provide clinical and safety guidance, support protocol design and data review, manage committees, and may supervise clinical colleagues; requires substantial clinical research experience in biopharma.
2w
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Lead Technology Product Manager, Clinical Decision Support Adoption & Engagement Analytics
Waltham or Madison or Coppell or Tampa or Draper or Philadelphia or Kennesaw or Dallas or Chicago or Indianapolis or Greenwood Village
$129k-$226k/yr HybridFull Time
5+ YOE5+ years in product, data, business analytics, or product operations; independent SQL querying; product telemetry, funnels, cohorts, dashboards, experimentation, and stakeholder communication experience.
SQL, A/B testing
3w
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RWE Project Lead
Cambridge, Massachusetts, United States
$149k-$215k/yr OnsiteFull Time
2+ YOEPhD or MSc in health sciences/epidemiology/public health with quantitative background; minimum 2 years RWE/clinical project experience in industry; project delivery, RWE/data analytics/statistics knowledge; therapeutic area and regulatory understanding.
3w
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Manager Statistical Programming
Cambridge or Warren
$129k-$210k/yr OnsiteFull Time
5+ YOEMaster's degree with 5+ years relevant programming experience (or 8-10 years), experience leading clinical study programming deliverables, project and people management experience, strong documentation skills in regulated environments.
SAS
3mo
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Manager Statistical Programming
Cambridge or Warren
$129k-$210k/yr OnsiteFull Time
8+ YOE5+ MgmtMaster’s degree required; 8-10 years of related experience; SAS certification desirable; experience leading programming for clinical trials; on-site role.
SAS, CDISC SDTM, CDISC ADaM
1mo
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Senior Manager, R&D Procurement - Clinical Labs and Diagnostics
Upper Providence or Waltham or Durham or Cambridge or Rockville or San Francisco
$114k-$190k/yr HybridFull Time
5+ YOEBachelor's degree,5+ years category management/procurement experience,experience leading complex negotiations and projects;pharmaceutical/healthcare preferred;advanced degree,AI and data analysis skills preferred.
AI
3mo
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Vice President, Biostatistics
Watertown or Watertown
$293k-$358k/yr HybridFull Time
15+ YOE5+ MgmtLead biostatistics strategy and team for oncology programs; design and oversight of clinical trials; regulatory readiness and vendor management.
SAS, R, Python, CDISC, Clinical trial design, Interim analyses
2mo
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GCP & GLP QA Lead (Nonclinical & Clinical Quality Assurance)
Boston, Massachusetts, United States
$171k-$257k/yr HybridFull Time
8+ YOEBachelor's in life sciences, 8+ years GLP/GCP QA experience, CRO/vendor oversight and inspection experience (FDA BIMO), GCP/GLP auditor certification preferred, knowledge of ICH E6/E8, TMF, data integrity, and audit execution.
ICH E6, ICH E8, TMF, eCOA, IRT
2w
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Director, Medical Lead - CNS
Raleigh or Woburn
HybridFull Time
10+ YOEDoctoral qualification required; 10+ years in pharmaceutical or biotech Medical Affairs, with expertise in lifecycle management, clinical research, regulatory frameworks, medical data, strategy, and cross-functional leadership.
Medical Science Liaisons (MSLs), RWE, HEOR
2w
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Lead Computer Systems Validation Engineer I (Clinical & R&D)
Waltham, Massachusetts, United States
$110k-$126k/yr HybridFull Time
7+ YOEBachelor’s degree in computer science, life sciences, engineering, or related field with 9+ years in digital quality; master’s with 7+ years considered. Requires GxP, CSV, quality systems, compliance, data integrity, and team leadership experience.
Learning Management System (LMS), Veeva DMS, TrackWise, TrackWise Digital, ValGenesis, GAMP 5, Artificial Intelligence (AI), Quality Risk Management, Change Control, CAPAs, SOPs
1mo
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Director, Patient Experience & Regulatory Engagement
Boston, Massachusetts, United States
$152k-$228k/yr OnsiteFull Time
10+ YOE10+ years in biotech/pharma with regulatory, clinical development, or consulting experience; bachelor\u0002s degree; experience generating/synthesizing patient experience data; ability to influence senior leaders and lead global initiatives.
1mo
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Senior Director, Biometrics
Cambridge, Massachusetts, United States
$263k-$321k/yr OnsiteFull Time
10+ YOEAdvanced degree in statistics/biostatistics/math, 10+ years in biometrics, expertise in clinical trial design, regulatory submissions, and leading biometrics/data management teams.
CDISC, SDTM, ADaM
3w
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Gastrointestinal & Inflammation (GI2) Therapeutic Area Head (TAH), Global Medical Safety
Boston, Massachusetts, United States
$321k-$504k/yr HybridFull Time
10+ YOE3+ MgmtMedical degree required,10+ years in pharmacovigilance/clinical research,3+ years people management,regulatory safety expertise,global pharmacovigilance experience,ability to synthesize complex data and lead cross-functional teams.
1w
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Executive Director, Head of US Rare Endocrinology and Rare Tumors
Boston, Massachusetts, United States
$282k-$423k/yr HybridFull Time
12+ YOE10+ MgmtAdvanced scientific or clinical degree required, with 12+ years of biopharmaceutical experience and 10+ years leading teams. Requires Medical Affairs strategy, rare disease, cross-functional leadership, and digital, data, and AI experience.
AI