72 manager clinical development jobs at 42 companies in Durham, NH
1mo
Save
Mark Applied
Hide
Executive Director, Clinical Development Lead
Lexington, Massachusetts, United States
$315k-$370k/yr OnsiteFull Time
8+ YOEMD/PhD/PharmD required, 8+ years in clinical research/drug development, experience leading clinical programs, IND/CTA submissions, strong trial design and regulatory knowledge, excellent communication and leadership.
2w
Save
Mark Applied
Hide
Senior Manager, Clinical Development and Validation
Burlington or New York City
$185k/yr HybridFull Time
5+ YOE5+ years diagnostic ultrasound/POCUS experience (registries required), ARDMS required, 3+ years R&D experience, bachelor's preferred, strong clinical-to-product translation and leadership, willingness to travel.
Compass AI, Butterfly Garden, Ultrasound-on-Chip, Butterfly iQ3
2w
Save
Mark Applied
Hide
Associate Director, Global Clinical Team Manager
Billerica, Massachusetts, United States
$145k-$200k/yr HybridFull Time
8+ YOEBachelor's degree and 8+ years in global pharmaceutical drug development, including 5+ years in clinical development, project management, or clinical program coordination; strong leadership and communication skills.
PMP, Integrated Evidence Plan (IEP), Biomarker Plan, Clinical Pharmacology Plan, protocols, CSRs, IBs
2w
Save
Mark Applied
Hide
Associate Director, Global Clinical Team Manager
Billerica, Massachusetts, United States
$145k-$200k/yr HybridFull Time
8+ YOEBachelor's degree in a relevant field, 8+ years in global pharmaceutical drug development, and 5+ years in clinical development, project management, or program coordination; PMP preferred.
Integrated Evidence Plan (IEP), Clinical Development Plans, Biomarker Plan, Clinical Pharmacology Plan, Clinical Team (CT), Global Clinical Lead (GCL), Global Program Head (GPH), Program Management Lead (PML), protocols, CSRs, IBs
1mo
Save
Mark Applied
Hide
Manager, Clinical Supplies
Burlington, Massachusetts, United States
HybridFull Time
3+ YOEBachelor's degree, 3+ years clinical supply management in pharma/biotech, IRT experience preferred, strong MS Excel/Word/PowerPoint skills, cross-functional communication, SOP development, global clinical supply and cold chain knowledge.
IRT, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
1mo
Save
Mark Applied
Hide
Principal Clinical Trial Manager
Andover, Massachusetts, United States
$137k-$194k/yr OnsiteFull Time
8+ YOEBA/BS in science or life sciences,8+ years clinical trial experience in pharma/biotech/CRO (8-10 preferred),experience with IRB/EC submissions,GCP/ICH/FDA knowledge,EDC experience,clinical budget and vendor management.
Electronic data capture (EDC)
1mo
Save
Mark Applied
Hide
Associate Director, Global Clinical Trial Manager
Billerica, Massachusetts, United States
$145k-$200k/yr HybridFull Time
8+ YOEBachelor's in life sciences or related,8+ years drug development,5+ years clinical development/project management in pharma/CRO,PMP preferred,master's preferred,familiarity with protocols/CSRs/IBs,strong communication and cross‑functional leadership.
2mo
Save
Mark Applied
Hide
Manger, Clinical Outreach, Boston
Boston or Woburn
$90k-$110k/yr FieldFull Time
3+ YOEBased in Greater Boston with ~75% travel. 3+ years in provider outreach/business development or related healthcare relationship role; strong presentation, CRM (HubSpot) experience, and ability to build referral partnerships; clinical licensure preferred.
HubSpot, CRM, HealthJoy
1mo
Save
Mark Applied
Hide
Oncology Senior Veterinary Clinical Research Manager
Westbrook, Maine, United States
$145k/yr HybridFull Time
DVM, PhD, or equivalent medical and scientific training; companion animal expertise; clinical research experience; strong communication, analytical, organizational, and collaboration skills; Microsoft Office and Excel proficiency.
Microsoft Office, Microsoft Excel
4w
Save
Mark Applied
Hide
Clinical Psychologist
Woburn, Massachusetts, United States
$63k-$114k/yr OnsiteFull Time
Doctoral degree in clinical psychology, experience in diverse public school settings, knowledge of child development, assessment administration and reporting, program development and staff supervision.
2mo
Save
Mark Applied
Hide
Executive Director, Clinical Program Management
Burlington or United States
$276k-$321k/yr HybridFull Time
Extensive biotech/pharma clinical development leadership across multi-stage programs; governance participation; strong cross-functional collaboration.
1mo
Save
Mark Applied
Hide
Manager, Global Clinical Supply Chain Planning
Lexington, Massachusetts, United States
$116k-$182k/yr OnsiteFull Time
4+ YOEDevelop end-to-end clinical supply plans, perform scenario and risk analysis, liaise with cross-functional teams, ensure GMP/GDP/GCP compliance, and use clinical supply systems; 4+ years pharma experience.
ClinApps Clinical Supplies Management Database (CSMD), Interactive Response Technology (IRT), Microsoft Excel, MS Project
1mo
Save
Mark Applied
Hide
Clinical Supervisor - ACCS
Malden, Massachusetts, United States
$75k-$80k/yr OnsiteFull Time
Master's-level or licensed clinician with experience working with adults with mental illness; able to conduct assessments, develop treatment plans, provide clinical supervision, and participate in on-call rotation. Valid Massachusetts driver's license preferred clinical license (LICSW/LCSW/LMHC/LRC/LADCI).
1mo
Save
Mark Applied
Hide
Director, Clinical Affairs of Coronary/Vascular
Plymouth or Cambridge or Colorado Springs or San Diego or Bedford or Bothell
$171k-$306k/yr OnsiteFull Time
10+ YOE5+ Mgmt10+ years clinical/scientific experience with coronary research, 5+ years managing clinical research teams, knowledge of FDA/GCP and global clinical regulations, Bachelor's degree required (advanced degree preferred), ability to travel 20–30%.
4d
Save
Mark Applied
Hide
Director, Clinical Data Management
Bedford or Waltham
$225k-$244k/yr HybridFull Time
10+ YOEBachelor’s degree in a scientific or healthcare discipline and 10+ years of clinical data management experience, including people leadership. Requires EDC, CDISC, GCP, regulatory compliance, and analytics expertise.
TANGO, EDC, eCOA, eDiary, ePRO, ClinRO, ObsRO, SAS, R, Python, Spotfire, Power BI, J-Review, Microsoft Outlook, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Project, Microsoft Visio, Medidata Rave, Veeva Vault CDMS, CDISC, CDASH, SDTM, ADaM, Define-XML, MedDRA, WHODrug, ALCOA+, E-Verify
2mo
Save
Mark Applied
Hide
Senior Clinical Trial Associate - Oncology
Bedford, Massachusetts, United States
$108k-$132k/yr HybridFull Time
3+ YOE3+ years on phase I-IV clinical studies in biotech/CRO/academic settings; strong knowledge of ICH/GCP, TMF management, vendor oversight, audit support, and cross-functional coordination. BS/BA/RN (preferred).
Microsoft Project
2mo
Save
Mark Applied
Hide
Registered Nurse Clinical Manager Home Care
Westford, Massachusetts, United States
$45-$55/hr FieldFull Time, Part Time
2+ YOEActive RN license, 2–3 years home health/hospice/skilled nursing experience, IV infusion expertise, CPR, driver and car with insurance, leadership and supervisory experience, care plan development, regulatory compliance and QA skills.
1mo
Save
Mark Applied
Hide
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
2w
Save
Mark Applied
Hide
Clinical Research Coordinator I - Colon and Rectal Surgery
Burlington, Massachusetts, United States
$22-$27/hr OnsiteFull Time
0+ YOECoordinate and implement clinical research studies, manage regulatory documents, recruit and consent participants, maintain study data and files, and support protocol adherence.
1mo
Save
Mark Applied
Hide
Manager Study Start-up
Aliso Viejo or San Clemente or Burlington or United States
$130k-$163k/yr OnsiteFull Time
8+ YOE8+ years clinical research experience in medical device/pharma; experience leading study execution, timelines, budgets, and cross-functional teams; strong knowledge of FDA regulations and GCP; risk management skills.
Explore Jobs