24 associate research director jobs at 11 companies in Durham, NH
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Associate Director, Research & Development
Manchester, New Hampshire, United States
OnsiteFull Time
4+ YOEPhD with ~4+ years experience in human stem cell biology or tissue engineering; experience leading R&D teams, assay development, ELN use, GLP familiarity, RNASeq and flow cytometry knowledge, and strong documentation skills.
ELN, GraphPad, JMP, RNASeq, flow cytometry
2mo
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Scientific Director/Associate Director, Clinical Pharmacology
Billerica, Massachusetts, United States
$168k-$261k/yr HybridFull Time
2+ YOERequires a relevant PhD, PharmD, or MD and 2+ years of pharmaceutical or postdoctoral clinical drug development experience; Scientific Director applicants require 5+ years. Expertise in clinical pharmacology and MIDD required.
Model Informed Drug Development (MIDD)
2mo
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Scientific Director/Associate Director, Clinical Pharmacology
Billerica, Massachusetts, United States
$168k-$261k/yr HybridFull Time
2+ YOEDoctorate in a relevant discipline and 2+ years of pharmaceutical or postdoctoral clinical drug development experience; 5+ years required for Scientific Director. Expertise in clinical pharmacology, MIDD, PK/PD, and cross-functional leadership.
Model Informed Drug Development (MIDD), PK/PD, Pharmacometrics, Biostatistics, Data Sciences, Clinical Biomarkers, Clinical Pharmacology, ADME, Exposure-QTc, GXP, Clinical Protocols, IBs, CTDs, INDs, NDAs, IMPDs
3w
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Associate Director - Value, Access, Insights, and Solutions
Cambridge or Lexington
$169k-$266k/yr HybridFull Time
5+ YOEMaster's or doctorate required; 5+ years healthcare experience including 2 years in pharma; payer/PBM experience; observational and outcomes research expertise; strong oral/written communication and cross-functional leadership.
VEEVA
2mo
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Scientific Director/Associate Director, Clinical Pharmacology (Billerica, Massachusetts, US, 01821)
Billerica, Massachusetts, United States
$168k-$261k/yr HybridFull Time
5+ YOE2+ years in pharma industry or postdoc in clinical drug development; doctorate in clinical pharmacology, pharmaceutics, pharmacometrics, statistics, engineering, or mathematics; strong CP and MIDD expertise.
3mo
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Business Insights & Strategy, Cardiology, NETs & Pipeline Associate Director
Bedford, Massachusetts, United States
$139k-$232k/yr OnsiteFull Time
7+ YOE7+ years in market research or commercial strategy in life sciences; expertise in qualitative and quantitative methods; strong communication and vendor management; BS/BA, advanced degree preferred.
2mo
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Associate Director, Formulation Development
Burlington or Carmel or Indianapolis
OnsiteFull Time
8+ YOE8+ years industrial experience in peptide or protein formulation and analytical development; expertise in parenteral and lyophilized formulations, SEC/RP-HPLC/LC-MS, stability studies, CMC regulatory knowledge, and strong communication skills.
PEP™ platform, SEC, RP-HPLC, LC-MS, subvisible particle analysis, lyophilization
3w
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Associate Director, Translational Toxicology, Preclinical Development
Lexington, Massachusetts, United States
$170k-$230k/yr OnsiteFull Time
7+ YOEDoctorate (DVM/PhD) in biology/toxicology,7+ years preclinical safety experience,GLP and regulatory toxicology expertise,experience with regulatory submissions and CRO oversight,ability to travel to monitor studies.
2mo
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Associate Director, Laboratory Informatics and Platform Automation
Lexington, Massachusetts, United States
$196k-$230k/yr OnsiteFull Time
10+ YOEPhD with 10+ years (or BS/MS with 15+ years) in laboratory informatics/automation for drug discovery; life sciences background (screening, biology, chemistry, DMPK, multi-omics/NGS); proven technical team leadership; deep LIMS/ELN/SDMS and automation integration experience.
LIMS, ELN, SDMS, Dotmatics, Snowflake, Opal Computational Platform, High-Res Cellario, Biosero Green Button Go, API
2mo
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Assoc. Director, Evidence Generation
Lexington, Massachusetts, United States
$191k-$264k/yr OnsiteFull Time
7+ YOE7+ years in evidence generation within pharma/CRO; advanced scientific degree (PhD/PharmD/MD or MS/MPH); experience leading registries; strong analytical, communication, and presentation skills; high proficiency in Microsoft Office and CoPilot; AI experience preferred.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, CoPilot, Microsoft Outlook, AI
3w
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Associate Director, Biostatistics
Woburn, Massachusetts, United States
$194k-$251k/yr RemoteFull Time
3+ YOEPhD or MS in Biostatistics/Statistics required, 3+ years (PhD) or 5+ years (MS) industry experience, SAS and SDTM/ADaM knowledge, oncology clinical trial and regulatory submission experience preferred.
SAS, SDTM, ADaM
1w
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Sr. Manager/Associate Director, Analytical Development & Quality Control
Indianapolis or Fishers or Lexington or Boston
OnsiteFull Time
8+ YOE4+ MgmtRequires a bachelor's degree, 8–10 years of biopharma or CDMO analytical/QC experience, 4 years of leadership, viral vector expertise, cGMP experience, and knowledge of laboratory systems and regulatory requirements.
qPCR, ddPCR, ELISA, Flow cytometry, LIMS, FDA, EMA, ICH, ALCOA+, Part 11, AAV, LVV, RVV
2d
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Principal Scientist / Associate Director, Process Analytical Technology (PAT) Lead
Woburn or Allston
$140k-$180k/yr HybridFull Time
10+ YOEPh.D. with 10+ years or M.S. with 12+ years in pharmaceutical or biotech PAT/process analytics; expertise in spectroscopy, image analysis, chemometrics, GMP manufacturing, control strategies, and regulatory submissions.
Process Analytical Technology (PAT), UV/Vis, NIR, Statistical Process Control (SPC), Real-Time Release Testing (RTRT), Partial Least Squares (PLS), Principal Component Analysis (PCA), Computer System Validation (CSV), GAMP 5, OpenCV, Python, Raman spectroscopy
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